CoChat
Sign Up
Cited by 434

The DOI matches its Crossref record.

Sesqui-, Di-, and triterpenoids as chemosystematic markers in extant conifers - A review

Otto, Angelika, Wilde, Volker·2001·The Botanical Review
DOI 10.1007/bf02858076
Open this paper in CoChat — free account

Overview

Integrity signals

Registry

Crossref · 10.1007/bf02858076

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

No references could be resolved yet.

Research works printed but not linked: 557

  1. Adams, R. P. 1990.Juniperus procera of East Africa: Volatile leaf oil composition and putative relationship toJuniperus excelsa. Biochem. Syst. Ecol. 18: 207–210. · DOI
  2. — 1991. Cedar wood oil—Analysis and properties. Pp. 159–173in H. F. Linskens & J. F. Jackson (eds.), Essential oils and waxes. Modern methods of plant analysis, n.s., 12. Springer-Verlag, Berlin. · DOI
  3. —,E. von Rudloff, T. A. Zanoni &L. Hogge. 1980. The terpenoids of an ancestral/advanced species pair ofJuniperus. Biochem. Syst. Ecol. 8: 35–37. · DOI
  4. —,T. A. Zanoni &L. Hogge. 1984. The volatile oils ofJuniperus flaccida var.flaccida and var.poblana. J. Nat. Prod. (Lloydia) 47: 1064–1065. · DOI
  5. —,S. Z. Zhang &G. L. Chu. 1995. Essential oil ofJuniperus formosana HAYATA leaves from China. J. Essential Oil Res. 7: 687–689. · DOI
  6. Agrawal, P. K. &R. P. Rastogi. 1981. Terpenoids fromCedrus deodara. Phytochemistry 20: 1319–1321. · DOI
  7. ——. 1984. Chemistry of the true cedars. Biochem. Syst. Ecol. 12: 133–144. · DOI
  8. Ahond, A., P. Garnero &B. Gastambide. 1964. Isolation of communic acid from the cones of a dwarf variety of cypress. Bull. Soc. Chim. France 1964: 348–349.
  9. Akiyoshi, S., H. Erdtman &T. Kubota. 1960. The identity of junipene, kuromatsuene and longifolene and of juniperol, kuromatsuol, macrocarpol and longiborneol. Tetrahedron 9: 237. · DOI
  10. Allen, F. H., J. P. Kutney, J. Trotter &N. D. Westcott. 1971. The structures and absolute stereochemistry of cyclograndisolide and epicyclograndisolide, novel triterpene lactones ofAbies grandis. Tetrahedron Lett. 1971: 282–286.
  11. Andersen, N. H. &D. D. Syrdal. 1970. Terpenes and sesquiterpenes ofChamaecyparis nootkatensis leaf oil. Phytochemistry 9: 1325–1340. · DOI
  12. Anderson, A. B. 1954. Rosin from Jeffrey pine stumpwood. Tappi 37: 316–320.
  13. —,R. Riffer &A. Wong. 1969. Monoterpenes, fatty and resin acids ofPinus ponderosa andPinus jeffreyi. Phytochemistry 8: 873–875. · DOI
  14. Aplin, R. T. &R. C. Cambie. 1964. Taxonomic distribution of some diterpene hydrocarbons. New Zealand J. Sci. (Wellington) 7: 258–260.
  15. —— &P. S. Rutledge. 1963. The taxonomic distribution of some diterpene hydrocarbons. Phytochemistry 2: 205–214. · DOI
  16. Appendino, G. 1995. The phytochemistry of the yew tree. Natural Prod. Rep. 12: 349–360. · DOI
  17. —,P. Gariboldi, A. Pisetta et al. 1992. Taxanes fromTaxus baccata. Phytochemistry 31: 4253–4257. · DOI
  18. Appleton, R. A., R. McCrindle &K. H. Overton. 1970. The diterpenes from the leaves ofCryptomeria japonica. Phytochemistry 9: 581–583. · DOI
  19. Arbuzov, B. A. &A. G. Khismatullina. 1958. Composition of rosin acids from resins ofPinus pithyusa andPinus insignis. Chem. Abstr. 52: 12823g.
  20. Arya, V. P. 1962. Neutral constituents of the bark extractive ofJuniperus commuais. J. Scientific & Industrial Res. (New Delhi) B21: 236–237.
  21. Avcibasi, H., H. Anil &M. Toprak. 1987. Four terpenoids fromCedrus lebanotica. Phytochemistry 26: 2852–2854. · DOI
  22. —,—— 1988. Terpene acids fromCedrus libani. Phytochemistry 27: 3967–3968. · DOI
  23. Baggaley, K. H., H. Erdtman &T. Norin. 1968. Some new cedrane derivatives fromJuniperus foetidissima WILLD. Configuration of cedrolic acid. Tetrahedron 24: 3399–3405. · DOI
  24. Balansard, G., A. Hannan, P. Bernard et al. 1976. Chemical composition of the fertilized female strobuli ofThuja: Thuja occidentalis L., I. Trav. Soc. Pharm. Montpellier 36: 231–237.
  25. Bambagiotti, M., F. F. Vincieri &G. Cosi. 1972. Monoterpene and sesquiterpene hydrocarbons ofPinus mugo. Phytochemistry 11: 1455–1460. · DOI
  26. Banthorpe, D. V., R. J. H. Duprey, J. F. Jones &C. M. Voller. 1977. Distribution of longibornane sesquiterpenes, I. Re-examination of some reported sources. Pl. Med. 31: 278–285. · DOI
  27. Barboni, L., P. Gariboldi, E. Torregiani et al. 1993. Taxanes from the needles ofTaxus wallichiana. Phytochemistry 33: 145–150. · DOI
  28. Bardyshev, I.I., L. Badam, R. I. Zen’ko et al. 1969. Properties and chemical composition of a mixture of terpenoids extracted from the oleoresin of Scotch pine. Chem. Abstr. 72: 51774z.
  29. Barnes, M. A. &W. C. Barnes. 1983. Oxic and anoxic diagenesis of diterpenes in lacustrine sediments. Pp. 289–298in M. Bjorøy (ed.), Advances in organic geochemistry, 1981. John Wiley & Sons, Chichester, England.
  30. Barrero, A. F., J. F. Sanchez &J. Altarejos. 1987. Resin acids in the woods ofJuniperus sabina L. andJuniperus oxycedrus L. Chem. Abstr. 110: 111701p.
  31. —,—,E. J. Alvarez-Manzaneda &M. Munoz Dorado. 1989. Sesquiterpenoids related to juvabione inAbies pinsapo. Phytochemistry 28: 2617–2619. · DOI
  32. —,—,J. E. Oltra et al. 1991. Oxygenated sesquiterpenes from the wood ofJuniperus oxycedrus. Phytochemistry 30: 1551–1554. · DOI
  33. —,—,E. J. Alvarez-Manzaneda et al. 1992. Diterpenoids and cyclolanostanolides fromAbies marocana. Phytochemistry 31: 615–620. · DOI
  34. —,—,—et al. 1993. Terpenoids and sterols from the wood ofAbies pinsapo. Phytochemistry 32: 1261–1265. · DOI
  35. —,—,—et al. 1994. Terpenoids in the wood ofAbies marocana. Phytochemistry 35: 1271–1274. · DOI
  36. —. 1996. Novel tricyclic sesquiterpenes fromJuniperus thurifera L. Chemical confirmation of the duprezianane skeleton. Tetrahedron Lett. 37: 3757–3760. · DOI
  37. Barreto, H. S.&C. Enzell. 1961. The chemistry of the natural order Cupressales 39. Heartwood constituents ofCupressus torulosa DON. Acta Chem. Scand. 15: 1313–1318. · DOI
  38. Baset, Z. H., R. J. Pancirov &T. R. Ashe. 1980. Organic compounds in coal: Structure and origin. Pp. 619–630in A. G. Douglas & J. R. Maxwell (eds.), Advances in organic geochemistry, 1979. Pergamon Press, Oxford.
  39. Batt, R. D. &C. H. Hassel. 1950. The essential oilof Libocedrus bidwillii, New Zealand cedar. J. Soc. Chemical Industry (London) 68: 359–361. · DOI
  40. Bennett, C. R. &R. C. Cambie. 1967. Chemistry of the Podocarpaceae, XIII. Constituents of the heartwoods ofPodocarpus nivalis HOOK, andP. acutifolius KIRK. Phytochemistry 6: 883–887. · DOI
  41. Berry, K. M., N. B. Perry &R. T. Weavers. 1985. Foliage sesquiterpenes ofDacrydium cupressinum: Identification, variation and biosynthesis. Phytochemistry 24: 2893–2898. · DOI
  42. Bisarya, S. C. &Sukh Dev. 1964. Allohimachalol, a new type in sesquiterpenoids. Tetrahedron Lett. 1964:3761–3765. · DOI
  43. Bol’shakova, V. I., L. I. Demenkova, E. N. Shmidt &V. A. Pentegova. 1988. Neutral diterpenoids in resin of five conifer species of Transcarpathia. Chem. Abstr. 111: 4244r.
  44. —,V. A. Khan, Z. V. Dubovenko et al. 1985. Terpenoids of the oleoresin ofLarix leptolepis. Chem. Abstr. 104: 183304k.
  45. Bower, C. L. &J. W. Rowe. 1967. Extractives of Jack pine bark: Occurrence of (+)-l3-epimanoyl oxide and related labdanes diterpenes. Phytochemistry 6: 151–153. · DOI
  46. Brandt, C. W. &B. R. Thomas. 1952a. Chemical differentiation of the generaPodocarpus andDacrydium. Nature 170: 1018. · DOI
  47. ——. 1952b. Resins of theDacrydium andPodocarpus genera: The wood resin fromDacrydium cupressinum. New Zealand J. Sci. Technol. B33: 30–37.
  48. Brassell S. C., G. Eglinton &J. R. Maxwell. 1983. The geochemistry of terpenoids and steroids. Biochem. Soc. Trans. 11: 575–586. · DOI
  49. Braun, S. &H. Breitenbach. 1977. Strukturaufklaerung einer neuen Diterpensäure ausMetasequoia glyptostroboides mit Hilfe der13-C NMR-Spektroskopie. Tetrahedron 33: 145–150. · DOI
  50. Brecknell, D. J. &R. M. Carman. 1978. Callitrin, callitrisin, dihydrocallitrisin, columellarin and dihydrocolumellarin, new sesquiterpene lactones from the heartwood ofCallitris columellaris. Tetrahedron Lett. 1978: 73–76. · DOI
  51. Bredenberg, J. B. 1957a. The non-occurrence of cedrene and cedrol inJuniperus communis L. Acta Chem.Scand. 11: 98–100. · DOI
  52. —. 1957b. Ferruginol and Δ9-dehydroferruginol. Acta Chem. Scand. 11: 932–935. · DOI
  53. Briasco, J. D. &J. Murray. 1952. Essential oils of New Zealand Podocarpaceae, I.Dacrydium colensoi. J. Appl. Chem. 2: 187–192. · DOI
  54. Briggs, L. H. 1937. The identity of dacrene and sciadopitene with phyllocladene. J. Chem. Soc. 1937: 79–80. · DOI
  55. —. 1940. Isolation of phyllocladene from the leaf oil ofPodocarpus hallii and its significance on the botanical classification of this species. Trans. Roy. Soc. New Zealand 70: 173–174.
  56. — &R. W. Cawley. 1948. Diterpenes, I. The identity of kaurene with podocarprene. J. Chem. Soc. 1948: 1888–1889. · DOI
  57. — &J. A. Loe. 1950. Diterpenes, IV. The isolation of phyllocladene from the essential oil ofPodocarpus spicatus grown in the North Island of New Zealand. J. Chem. Soc. 1950: 958–959. · DOI
  58. — &M. D. Sutherland. 1942. The essential oil ofCupressus macrocarpa. J. Organic Chem. 7: 397–407. · DOI
  59. —. 1948. The essential oil ofPhyllocladus trichomanoides. J. Organic Chem. 13: 1–9. · DOI
  60. — &G. W. White. 1975. Constituents of the essential oil ofAraucaria araucaria. Tetrahedron 31: 1311–1314. · DOI
  61. —,R. W. Cawley, J. A. Loe &W. I. Taylor. 1950. Diterpenes, III. The diterpenes fromPodocarpus ferrugineus. J. Chem. Soc. 1950: 955–958. · DOI
  62. —,R. C. Cambie, R. N. Seelye &A. D. Warth. 1959. Chemistry of the Podocarpaceae, IV. Constituents of the heartwood ofPodocarpus dacrydioides A. RICH. Tetrahedron 7: 270–276. · DOI
  63. —,M. Kingsford &G. W. White. 1974. New Zealand phytochemical survey, 10. Essential oil ofAgathis australis. New Zealand J. Sci. (Wellington) 17: 9–12.
  64. Brooker, E. G. 1959. Constituents ofPhyllocladus glaucus. New Zealand J. Sci. 2: 212–214.
  65. Brossi, A. &O. Jeger. 1950. Zur Kenntnis der Diterpene 59. Über die Identität der Miropinsäure und der Isodextropimarsäure. Helv. Chim. Acta 33: 722–724. · DOI
  66. Brummit, R. K., comp. 1992. Vascular plant families and genera. Roy. Bot. Gard., Kew, London.
  67. Bruns, K. &G. Weissmann. 1966. Die Konfiguration der Diterpene ausAraucaria imbricata PAVON (A. araucana). Tetrahedron Lett. 1966: 1901–1903. · DOI
  68. Brunsfeld, S. J., P. S. Soltis D. E. Soltis et al. 1994. Phylogenetic relationships among the genera of Taxodiaceae and Cupressaceae: Evidence fromrbcL Sequenzen. Syst. Bot. 19: 253–262. · DOI
  69. Bulgakov, A. N. 1988. Terpenoid composition of balsams ofPinus taeda L.,P. maritima LAMB.,P. pseudostrobus andP. contorta DOUGL. introduced in the U.S.S.R. Chem. Abstr. 109:89785z.
  70. Cairness, D. A., R. L. Eagan, O. Ekundaya &D. G. I. Kingston 1983. Plant anticancer agents, XIII. Constituents ofAustrocedrus chilensis. J. Nat. Prod. (Lloydia) 46: 135–139. · DOI
  71. Cambie, R. C. &L. N. Mander. 1961. The absolute configuration of hydroxytotarol. Chemistry & Industry (London) 1961: 1877–1878.
  72. ——. 1962. Chemistry of the Podocarpaceae, VI. Constituents of the heartwood ofPodocarpus totara G. BENN. Tetrahedron 18: 465–475. · DOI
  73. ——. 1964. Extractives ofDacrydium biforme. New Zealand J. Sci. 7: 188–195.
  74. —,W. R. J. Simpson &L. D. Colebrook 1963. Chemistry of the Podocarpaceae, VII. Podototarin and the constituents of the heartwood ofPodocarpus hallii KIRK. Tetrahedron 19: 209–217. · DOI
  75. —,P. K. Grant, C. Huntrakul &R. J. Weston. 1969. Diterpenes ofDacrydium kirkii. Austral. J. Chem. 22: 1691–1697. · DOI
  76. —,R. J. Madden &J. C. Parnel. 1971. Chemistry of the Podocarpaceae, 28. Constituents of some Podocarpus—and other species. Austral. J. Chem. 24: 217–221. · DOI
  77. —,I. R. Burfitt, T. E. Goodwin &E. Wenkert. 1975. The structure of hallol. J. Organic Chem. 40: 3789–3791. · DOI
  78. —,B. A. Grigor &T. Mee-Ing. 1981. Chemistry of the Podocarpaceae, LVI. Resin acids fromPhyllocladus trichomanoides. Austral. J. Chem. 34: 1073–1078. · DOI
  79. —,R. E. Cox, K. D. Croft &D. Sidwell. 1983. Phenolic diterpenoids of some Podocarps. Phytochemistry 22: 1163–1166. · DOI
  80. —— &D. Sidwell. 1984. Phenolic diterpenoids ofPodocarpus ferrugineus and other Podocarps. Phytochemistry 23: 333–336. · DOI
  81. —,J. M. Coddington, M. J. Stone et al. 1989. Diterpenoids from the wood ofAgathis vitiensis. Phytochemistry 28: 1675–1679. · DOI
  82. Caputo, R. &L. Mangoni. 1974. Diterpenes fromAraucaria bidwillii. Phytochemistry 13: 467–470. · DOI
  83. —,— &P. Monaco. 1972. Diterpenesof Araucaria excelsa. Phytochemistry 11: 839–840. · DOI
  84. —,——. 1974a. Araucariaceae, III. Two new labdane norditerpenediols fromAraucaria excelsa. Gazz. Chim. Ital. 104: 491–498.
  85. —,—,— &L. Previtera. 1974b. New labdane diterpenes fromAraucaria cookii. Phytochemistry 13:471–174. · DOI
  86. —,V. Dovinola &L. Mangoni. 1974c. New diterpenes fromAraucaria cunninghamii. Phytochemistry 13:475–478. · DOI
  87. —,L. Mangoni, P. Monaco &L. Previtera. 1975. Araucariaceae, V. Diterpenes fromAraucaria angustifolia. Gazz. Chim. Ital. 105: 639–642.
  88. Carman, R. M. &D. E. Cowley. 1967. Diterpenoids, XII. “Dundatholic acid.” Austral. J. Chem. 20: 193–196.
  89. — &H. C. Deeth. 1967. Diterpenoides, XIV. 4-Epidehydroabietic acid from the oleoresin ofCallitris columellaris. Austral. J. Chem. 20: 2789–2793. · DOI
  90. —— 1971. Diterpenoids, XXVI. New diterpenoid acid from the oleoresin ofCallitris columellaris. Austral. J. Chem. 24: 353–359. · DOI
  91. — &N. D. Dennis. 1964. Diterpene acids ofAgathis robusta oleoresin. Austral. J. Chem. 17: 390–392. · DOI
  92. — &P. K. Grant. 1961. Biformene. J. Chem. Soc. 1961: 2187–2191. · DOI
  93. — &R. A. Marty. 1966. Diterpenoids, IX.Agathis microstachya oleoresin. Austral. J. Chem. 19: 2403–2406. · DOI
  94. ——. 1968. Diterpenoids, XVI. Agathalic acid—A new naturally occurring diterpenoid. Austral. J. Chem. 21: 1923–1925.
  95. -,R. E. Corbett, P. K. Grant et al. The diterpenesof Dacrydium colensoi, V. Tetrahedron Lett. 1966:3173–3179. · DOI
  96. —,W. J. Craig &I. M. Shaw. 1973. Diterpenoids, XXXI. Three new resin acids. Austral. J. Chem. 26: 209–214. · DOI
  97. Cassady, J. M., T. K. Lightner, T. G. McCloud et al. 1984. Revised structure of podolactone C, the antileukemic componentof Podocarpus milanjanus RENDLE. J. Organic Chem. 49: 942–945. · DOI
  98. Chalchat, J. C., R. P. Garry, A. Michet &A. Remery. 1985. The essential oils of two chemotypes ofPinus sylvestris. Phytochemistry 24: 2443–2444. · DOI
  99. Chaw, S.-M., H. Long, B.-S. Wang et al. 1993. The phylogenetic position of Taxaceae based on 18S rRNA sequences. J. Molec. Evol. 37: 624–630.
  100. —,H.-M. Sung, H. Long et al. 1995. The phylogenetic positions of the conifer generaAmento-taxus, Phyllocladus, andNageia inferred from 18S rRNA sequences. J. Molec. Evol. 41:224–230.
  101. —,A. Zharkikh, H.-M. Sung et al. 1997. Molecular phylogeny of extant gymnosperms and seed plant evolution: Analysis of nuclear 18S rRNA sequences. Molec. Biol. & Evol. 14: 56–68. · DOI
  102. Chen, W., P. Chang, B. Wu &Q. Zheng. 1991. Studies of the chemical constituents ofTaxus yunnanensis. Chem. Abstr. 116: 191082z.
  103. Cheng, Y. S. &M. D. Tsai. 1972. Terpenes and sterols ofCunninghamia konishii. Phytochemistry 11: 2108–2109. · DOI
  104. — &E. von Rudloff. 1970. The volatile oil of the leaves ofChamaecyparis nootkatensis. Phytochemistry 9: 2517–2527. · DOI
  105. —,T. Nishino &T. Toda. 1971. Essential oil components of the Benihi tree. Chem. Abstr. 76: 70134q.
  106. —,E. H. T. Chen &G. J. M. Fang. 1975. The neutral part of the bark ofPinus luchuensis MAYER. Chem. Abstr. 84: 132658q.
  107. Cherches, K. A., I.I. Bardyshev &O. T. Tkachenko. 1960. Resin acids from the oleoresin of Ayansk spruce. Chem. Abstr. 55: 7466d.
  108. —,—,A. N. Bulgakov &E. A. Akinchits. 1965. Resin acids of the oleoresinsof Pinus pityusa andPinus pallasiana and their hybrid. Chem. Abstr. 64: 10090b.
  109. Chernenko, G. F., L. I. Demenkova, E. E. Ivanova &E. N. Shmidt. 1990. Extractives from the bark ofPicea ajanensis. Chem. Abstr. 115: 25973a.
  110. Chernyaeva, G. N. &T. V. Barakov. 1983. Seasonal dynamics ofAbies sibirica essential oils. Chem. Abstr. 100: 135959y.
  111. Cheung, H. T. A., T. Miyase, M. P. Lenguyen &M. A. Smal. 1993. Further acidic constituents and neutral componentsof Pinus massoniana resin. Tetrahedron 49: 7903–7915. · DOI
  112. —,S. L. Fu &M. A. Smal. 1994. Inhibition of a platelet aggregation by diterpene acids fromPinus massoniana resin. Arzneimittelforsch. 44: 17–25.
  113. Chirkova, M. A. &V. A. Pentegova. 1962. The sesquiterpenes ofAbies sibirica. Chem. Abstr. 57: 14183b.
  114. —. 1969. Neutral substances inAbies sibirica oleoresin, II. Structure of neoabienol. Chem. Abstr. 72: 32057b.
  115. Chow, Y. L. &H. Erdtman. 1962. The chemistry of the natural order Cupressales 42. Heartwood constituents ofTetraclinis articulata (VAHL) MAST. Acta Chem. Scand. 16: 1291–1295. · DOI
  116. Chu, A., J. Zajicek, L. B. Davin et al. 1992. Mixed acetoxy-benzoxy taxanes esters fromTaxus brevifolia. Phytochemistry 31: 4249–4249. · DOI
  117. Clarke, D. B., S. F. R. Hinkley &R. T. Weavers. 1997. Waihoensene: A new laurenene-related diterpene fromPodocarpus totara var.waihoensis. Tetrahedron Lett. 38: 4297–4300. · DOI
  118. Conner, A. H. &J. W. Rowe. 1977. New neutral diterpenes from southern pine tall oil. Phytochemistry 16: 1777–1781. · DOI
  119. —,B. A. Nagasampagi &J. W. Rowe. 1980. Terpenoid and other extractives of western white pine bark. Phytochemistry 19: 1121–1131. · DOI
  120. —,T. P. Haromy &M. Sundaralingam. 1981. 30-Nor-3b-methoxyserrat-14-en-21-one: First reported natural occurrence of a norserratene triterpene. J. Organic Chem. 46: 2987–2988. · DOI
  121. Cool, L. G. 1996. Sesquiterpene alcohols from foliage ofFitzroya cupressoides. Phytochemistry 42: 1015–1019. · DOI
  122. — &K. Jiang. 1995a. Thujopsene and cis-muurolane-related sesquiterpenoids fromCupressus bakeri. Phytochemistry 40: 177–181. · DOI
  123. —— 1995b. A seco-amorphane tri-ether fromCupressus macnabiana foliage. Phytochemistry 40:857–859. · DOI
  124. —,A. B. Power &E. Zavarin. 1991. Variability of foliage terpenes ofFitzroya cupressoides. Biochem. Syst. Ecol. 19:421–432. · DOI
  125. Coppen, J. W., C. Gay, D. J. James et al. 1993a. Variability in xylem resin composition amongst natural populations of IndonesianPinus merkusii. Phytochemistry 33: 129–136. · DOI
  126. —,—,—et al. 1993b. Xylem resin composition and chemotaxonomy of three varieties ofPinus caribaea. Phytochemistry 33: 1103–1 111. · DOI
  127. Corbett, R. E. &W. G. Hanger. 1954. The structure of metrosiderene. J. Chem. Soc. 1954:1179–1181. · DOI
  128. — &R. A. J. Smith. 1967a. Diterpenes from the volatile oil ofDacrydium colensoi. J. Chem. Soc. C 1967: 300–302. · DOI
  129. —— 1967b. Selin-11-en-4a-ol from the essential oilof Podocarpus dacrydioides. Tetrahedron Lett. 1967: 1009–1012. · DOI
  130. — &L. C. K. Wong. 1956. Volatile oil ofDacrydium biforme. J. Sci. Food Agric. 6: 739–743. · DOI
  131. —,D. R. Lauren &R. T. Weavers. 1979. The structure of laurenene, a new diterpene from the essential oil ofDacrydium cupressinum. J. Chem. Soc. Perkin Trans. 1 1979: 1774–1790. · DOI
  132. Couchman, F. M. &E. von Rudloff. 1965. Gas-liquid chromatography of terpenes, XIII. The volatile oil of the leavesof Juniperus horizontalis MOENCH. Canad. J. Chem. 43: 1017–1021. · DOI
  133. Crawford, D. J. &D. E. Giannasi. 1982. Plant Chemosystematics. BioScience 32: 114–124. · DOI
  134. Das, B., S. P. Rao, K. V. N. S. Srinivas et al. 1995. A taxoid from needles of HimalayanTaxus baccata. Phytochemistry 38: 671–674. · DOI
  135. Dauben, W. G. &V. F. German. 1966. The structure of lambertianic acid, a new diterpenic acid. Tetrahedron 22: 679–683. · DOI
  136. —,B. Weinstein, P. Ilm &A. B. Anderson. 1961. The structure of δ-cadinol. Tetrahedron 15: 217–222. · DOI
  137. Dawidar, A. M., S. T. Ezmirly &M. Abdel-Mogib. 1991. Sesquiterpenes and diterpenes fromJuniperus phoenicea L. Pharmazie 46: 472–473.
  138. Dembitskii, A., R. A. Yuring, L. A. Ignatova &M. I. Goryaev. 1969. Substances found in essential oils, L. Composition ofJuniperus pseudosabina essential oil. Chem. Abstr. 73: 28759k.
  139. Deng, J., J. Liu &S. Zhao. 1997. Diterpenes from the root bark of Chinese fir (Cunninghamia lanceolata). Chem. Abstr. 127: 260112a.
  140. De Paiva Campello, J. &S. Ferreira Fonseca. 1975. Diterpenes fromAraucaria angustifolia. Phytochemistry 14: 2299–2300. · DOI
  141. —,—,C. J. Chang &E. Wenkert. 1975. Terpenes ofPodocarpus lambertius. Phytochemistry 14: 243–248. · DOI
  142. De Pascual Teresa, J., A. San Feliciano &J. M. del Corral. 1974. Components ofJuniperus oxycedrus fruits. An. Quim. 70: 1015–1019.
  143. —,I. S. Bellido, A. San Feliciano &A. Barrero. 1976. Components ofJuniperus communis L. fruits, II. Essential oil. An. Quim. 72: 657–660.
  144. —,S. San Feliciano, T. Egido &A. F. Barrero. 1977a. Components ofJuniperus thurifera L. berries, II. 8-α-Acetoxyelemol. An. Quim. 73: 151–152.
  145. —,A. F. Barrero, A. San Feliciano &I. Sanchez Bellido. 1977b. Components of the berries ofJuniperus communis L., IV. Neutral fraction. An. Quim. 73: 568–573.
  146. —,—,— &M. C. Caballero. 1978a. Components of the berries ofJuniperus oxycedrus L., V. γand β1-bulgarene. An. Quim. 73: 1527–1528.
  147. —,A. San Feliciano, M. L. Tabernero et al. 1978b. Components of the berries ofJuniperus phoenicea L., I. Acid fraction. An. Quim. 74: 459–464.
  148. —,— &A. F. Barrero. 1978c. Components of the berriesof Juniperus phoenicea L., II. Neutral fraction. An. Quim. 74: 465–469.
  149. —,A. F. Barrero, M. C. Caballero &A. San Feliciano. 1978d. Components ofJuniperus oxycedrus berries, VI. Essential oil. An. Quim. 74: 966–971.
  150. —,—,——. 1978e. Components ofJuniperus sabina L. berries, I. Hydrocarbons of essential oil. An. Quim. 74: 1093–1096.
  151. —,—,A. San Feliciano &M. C. Caballero. 1980a. Components of the essential oils ofJuniperus thurifera berries. Chem. Abstr. 93: 245243e.
  152. —,—,L. Muriel et al. 1980b. New natural diterpene acids fromJuniperus communis. Phytochemistry 19: 1153–1156. · DOI
  153. —,S. San Feliciano, J. M. del Corral &A. F. Barrero. 1983. Terpenoids fromJuniperus sabina. Phytochemistry 22: 300–301. · DOI
  154. Dhar, K. L., O. P. Suri, S. Sood &R. P. Sood. 1990. Three new labdane diterpenes from leaves and twigs ofJuniperus pseudosabina HOOK, andp2D-NMR-studies of 3-acetoxymanool. Indian J. Chem., B. 29:911–917.
  155. Ding, T., H. Liu &Q. Pu. 1982. Studies on the resin constituents of Taxodiaceae, I. Sesquiterpene and diterpene components. Chem. Abstr. 98: 86222g.
  156. Doi, K. &T. Kawamura. 1972. A new diterpene fromJuniperus rigida. Phytochemistry 11: 841–842. · DOI
  157. — &T. Shibuya. 1972a. Sesquiterpenes ofJuniperus conferta. Phytochemistry 11: 1174. · DOI
  158. ——. 1972b. Diterpenes ofJuniperus conferta. Phytochemistry 11: 1175. · DOI
  159. ——,T. Matsuo &S. Miki. 1971. Longifol-7(15)-en-5β-ol and longifol-3α,7α-oxide: New sesquiterpenes fromJuniperus conferta PARL. Tetrahedron Lett. 1971: 4003–4006. · DOI
  160. Do Khac, D., J. Bastard &M. Fetizon. 1979. Acide nor-anticopalique d’Agathislanceolata. Phytochemistry 18: 1839–1842. · DOI
  161. Dolejs, L. &V. Herout. 1961. Composition of the oil and root extract fromFokienia hodginsii. Chem. Abstr. 56: 7367g.
  162. Drebushchak, T. D., E. N. Shmidt, V. A. Khan et al. 1982. Terpenoid resins ofPinus pithyusa andPinus eldarica. Chem. Abstr. 97: 159493n.
  163. Dubovenko, Z. V., V. A. Babkin &V. A. Pentegova. 1970a. Sesquiterpenoids ofPicea ajanensis andPinus koraiensis oleoresin. Chem. Abstr. 75: 137513n.
  164. —,M. A. Chirkova, N. K. Kashtanova et al. 1970b. Siberian conifer resin sesquiterpenoids. Chem. Abstr. 76: 23030t.
  165. Dyachenko, L. G., V. I. Roshchin, V. E. Kovalev et al. 1986. Neutral compounds of extractible substance ofLarix gmelini. Chem. Abstr. 105: 75875j.
  166. Eberhardt, T. L., J. S. Han, J. A. Micales &R. A. Young. 1994. Decay resistance in conifer seed cones: Role of resin acids as inhibitors of decomposition by white-rot fungi. Holzforsch. 48: 278–284. · DOI
  167. Eckenwalder, J. E. 1976. Re-evaluation of Cupressaceae and Taxodiaceae: A proposed merger. Madroño 23: 237–300.
  168. Edwards, O. E., A. Nicholson &M. N. Rodger. 1960. The structure of sandaracopimaric acid. Canad. J. Chem. 38: 663–667. · DOI
  169. Eglinton G. &G. A. Logan. 1991. Molecular preservation. Philos. Trans. Roy. Soc. London, B, 333: 315–328. · DOI · Paper page
  170. Ekundayo, O. 1980a. Essential oils, III. Analysis of Table Mountain pine (Pinus pungens LAMB.) needle oil by gas chromatography-mass spectrometry (GC/MS). J. Chromatogr. Sci. 18: 368–369. · DOI
  171. Ekundayo, O. 1980b. Essential oils, IV. Composition of the volatile leaf (needle) oils ofPinus species. Z. Pflanzenphysiol. 99: 235–239. · DOI
  172. Enzell, C. &M. Krolikowska. 1963. The chemistry of the natural order Cupressales 48. Heartwood constituents ofCupressus arizonica GREENE. Ark. Kemi 20: 157–162.
  173. — &O. Theander. 1962. The constituents of conifer needles, II. Pinifolic acid, a new diterpene acid isolated fromPinus sylvestris L. Acta Chem. Scand. 16: 607–614. · DOI
  174. Erdtman, H. 1955. The chemistry of heartwood constituents of conifers and their taxonomic importance. Experientia, Suppl. II: 156–180.
  175. —. 1968. Chemical principles in chemosystematics. Rec. Adv. Phytochem. 1: 13–26.
  176. — &J. Hamatha. 1979. Phenolic and terpenoid heartwood constituents ofLibocedrus yateensis. Phytochemistry 18: 1495–1500. · DOI
  177. — &T. Norin. 1966. The chemistry of the order Cupressales. Progr. Chem. Organic Natural Prod. 24: 207–287.
  178. — &Z. Pelchowicz. 1955. The chemistry of the natural order Cupressales, XV. Heartwood constituents ofAustrocedrus chilensis (DON) FLORIN et BOUTELJE. Acta Chem. Scand. 9: 1728–1729. · DOI
  179. — &B. R. Thomas. 1958. The chemistry of the natural order Cupressales, XX. Heartwood constituents of the genusWiddringtonia. Acta Chem. Scand. 12: 267–273. · DOI
  180. — &J. G. Topliss. 1957. The chemistry of the natural order Cupressales, XVIII. Nootkatene, a new sesquiterpene type hydrocarbon from the heartwood ofChamaecyparis nootkatensis (LAMB.) SPACH. Acta Chem. Scand. 11: 1157–1161. · DOI
  181. — &H. Vorbrüggen. 1960. Die Chemie der natürlichen Ordnung Cupressales XXXII. Über die Inhaltsstoffe des Kernholzes vonAthrotaxis selaginoides DON,A. cupressoides DON undChamaecyparis pisifera SIEB, et ZUCC. Acta Chem. Scand. 14: 2161–2168. · DOI
  182. — &L. Westfelt. 1963. The neutral diterpenes from pine wood resin. Acta Chem. Scand. 17: 1826–1827. · DOI
  183. —,B. Kimland &T. Norin. 1966. Wood constituents ofDucampopinus krempfii (LECOMTE) CHEVALIER (Pinus krempfii LECOMTE). Phytochemistry 5: 927–931. · DOI
  184. —,—,— &P. J. L. Daniels. 1968. The constituents of the “pocket resin” from Douglas firPseudotsuga menziesii (MIRB.) FRANCO. Acta Chem. Scand. 22: 938–942. · DOI
  185. Ettouati, L., A. Ahond, O. Convert et al. 1988. Plants from New Caledonia, 114. Taxanes isolated from the leaves ofAustrotaxus spicata COMPTON (Taxaceae). Bull. Soc. Chim. France 1988: 749–755.
  186. Fang, J. M., S. K. Wu &Y. S. Cheng. 1985. A study of the constituents of the bark ofTsuga chinenesis PRITZ. var.formosana. J. Chin. Chem. Soc. 32: 477–480. · DOI
  187. —,S. T. Jan &Y. S. Cheng. 1987. Terpenoids fromCalocedrus formosana. Phytochemistry 26: 853–854. · DOI
  188. —,W. C. Su, W. C. Chuan &Y. S. Cheng. 1989a. A study of the constituents of the wood of Armand pine. J. Chin. Chem. Soc. 36: 483–485. · DOI
  189. —,K. C. Hsu &Y. S. Cheng. 1989b. Terpenoids from leaves ofCalocedrus formosana. Phytochemistry 28: 1173–1175. · DOI
  190. —,W. Y. Tsai &Y. S. Cheng. 1991a. Serratene triterpenoids fromPinus armandii bark. Phytochemistry 30: 1333–1336. · DOI
  191. —,C. I. Lang, W. L. Chen &Y. S. Cheng. 1991b. Diterpenoid acids from the leaves of Armand pine. Phytochemistry 30: 2793–2795. · DOI
  192. —,C. K. Lee &Y. S. Cheng. 1993a. Diterpenes from leaves ofJuniperus chinensis. Phytochemistry 33: 1169–1172. · DOI
  193. —,Y. C. Sou, Y. H. Chiu &Y. S. Cheng. 1993b. Diterpenes from the bark ofJuniperus chinensis. Phytochemistry 34: 1581–1584. · DOI
  194. —,Y. C. Chen, B. W. Wang &Y. S. Cheng. 1996. Terpenes from the heartwoodof Juniperus chinensis. Phytochemistry 41: 1361–1365. · DOI
  195. Fang, S., Y. Xu, Y. Li &M. Chen. 1990. Fleurylactones, a new type of sesquiterpene dilactone fromPodocarpus fleuryi HICKLE. Chem. Abstr. 113: 55897e.
  196. Figueiredo, M. R., M. A. C. Kaplan &O. R. Gottlieb. 1995. Diterpenes, taxonomic markers? Pl. Syst. & Evol. 195:149–158. · DOI
  197. Fleck, E. E. &S. Palkin. 1939. The presence of dihydroabietic acid in pine oleoresin and rosin. J. Amer. Chem. Soc. 61: 1230–1232. · DOI
  198. Florin, R. 1948. On the morphology and relationships of the Taxaceae. Bot. Gaz. (Crawfordsville) 110: 31–39. · DOI
  199. —. 1951. Evolution in Cordaites and Conifers. Acta Horti Berg. 15: 285–388.
  200. Fozdar, B. I., S. Khaan &K. M. Shansuddin. 1989. Norditerpenenedilactones, macrophyllic acid and biflavones fromPodocarpus latifolius. J. Indian Chem. Soc. 66: 423–424.

200 of 557 shown

Cited by

Sorted by citations

Metadata

Authors
Otto, A., & Wilde, V.
Venue
The Botanical Review
Publisher
Springer Science and Business Media LLC
Published
2001-04
Volume
67
Issue
2
Pages
141-238
ISSN
  • 0006-8101
  • 1874-9372
DOI
10.1007/bf02858076
Cited by
434
References
0
Language
en
Licence

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review