The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
13C-2H correlation NMR spectroscopy studies of the in vivo transformations of natural products from Artemisia annua
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The tertiary allylic hydroperoxide 481 is a biosynthetic intermediate linking dihydroartemisinic acid (480) and artemisinin (495), as shown by in vivo experiments with labeled dihydroartemisinic acid (480).
“The tertiary allylic hydroperoxide 481, which is produced in step i), has already been shown to be a biosynthetic intermediate, linking dihydroartemisinic acid (480) and artemisinin (495), by in vivo experiments with labeled dihydroartemisinic acid (480) [185,189].”
From The Biosynthesis of Artemisinin (Qinghaosu) and the Phytochemistry of Artemisia annua L. (Qinghao) (2010) · cites this paper as [189]
Citations
Cites
An improved method for heteronuclear chemical shift correlation by two-dimensional NMR
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Haynes, R. K., & Vonwiller, S. C. (1997) · Accounts of Chemical Research · doi:10.1021/ar950058w · Cited by 220
The mechanism of the spontaneous autoxidation of dihydroartemisinic acid
Sy, L.-K., & Brown, G. D. (2002) · Tetrahedron · doi:10.1016/s0040-4020(01)01193-0 · Cited by 129
Wallaart, T. E., van Uden, W., Lubberink, H. G. M., Woerdenbag, H. J., Pras, N., & Quax, W. J. (1999) · Journal of Natural Products · doi:10.1021/np980370p · Cited by 129
Two New Compounds from Artemisia annua
Brown, G. D. (1992) · Journal of Natural Products · doi:10.1021/np50090a006 · Cited by 70
Sy, L., Brown, G. D., & Haynes, R. K. (1998) · Tetrahedron · doi:10.1016/s0040-4020(98)00148-3 · Cited by 66
Three sesquiterpenes from Artemisia annua
Sy, L., & Brown, G. D. (1998) · Phytochemistry · doi:10.1016/s0031-9422(97)01047-9 · Cited by 62
Sy, L.-K., & Brown, G. D. (2001) · Phytochemistry · doi:10.1016/s0031-9422(01)00358-2 · Cited by 36
García‐Martín, M. L., Garcia-Espinosa, M. A., Ballesteros, P., Bruix, M., & Cerdán, S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m107501200 · Cited by 31
Sy, L.-K., Zhu, N.-Y., & Brown, G. D. (2001) · Tetrahedron · doi:10.1016/s0040-4020(01)00711-6 · Cited by 27
A new technique for the exact determination of 13C1H spin-spin coupling constants
Günther, H., Seel, H., & Schmickler, H. (1977) · Journal of Magnetic Resonance (1969) · doi:10.1016/0022-2364(77)90266-9 · Cited by 21
Schmitt, P., Wesener, J. R., & Günther, H. (1983) · Journal of Magnetic Resonance (1969) · doi:10.1016/0022-2364(83)90178-6 · Cited by 18
The use of deuterium as a nucleus for locking, shimming, and measuring NMR at high magnetic fields
van Zijl, P. C. M. (1987) · Journal of Magnetic Resonance (1969) · doi:10.1016/0022-2364(87)90039-4 · Cited by 16
Hoffman, R. E., Treitel, N., & Rabinovitz, M. (2001) · Magnetic Resonance in Chemistry · doi:10.1002/mrc.865 · Cited by 10
Complete editing of 13C spectra of CD H groups using the UPT sequence plus gated 1H decoupling
Bendall, M. R., Pegg, D. T., Wesener, J. R., & Günther, H. (1984) · Journal of Magnetic Resonance (1969) · doi:10.1016/0022-2364(84)90167-7 · Cited by 7
Flagged first, then by citations
Research works printed but not linked: 3
- Ho KF (2000) The Biogenesis of Artemisinin (Chapter 4). M. Phil. Dissertation, The University of Hong Kong, Hong Kong.
- Kim NC & Kim SU (1992) Biosynthesis of artemisinin from 11,12-dihydroartemisinic acid. J. Korean Agric. Chem. Soc. 35: 106–109.
- Liu JM, Ni MY, Fan YF, Tu YY, Wu ZH, Wu YL & Zhou WS (1979) Artemisinin. ActaChim. Sin. 37: 129–141.
Cited by
Sorted by citations
The Biosynthesis of Artemisinin (Qinghaosu) and the Phytochemistry of Artemisia annua L. (Qinghao)
Brown, G. D. (2010) · Molecules · doi:10.3390/molecules15117603 · Cited by 363
Self-citationIn vivo transformations of dihydroartemisinic acid in Artemisia annua plants
Brown, G. D., & Sy, L.-K. (2004) · Tetrahedron · doi:10.1016/j.tet.2003.11.070 · Cited by 183
In vivo transformations of artemisinic acid in Artemisia annua plants
Brown, G. D., & Sy, L.-K. (2007) · Tetrahedron · doi:10.1016/j.tet.2007.06.062 · Cited by 100
Fraga, B. M. (2005) · Natural Product Reports · doi:10.1039/b501837b · Cited by 77
NMR analysis of plant nitrogen metabolism
Mesnard, F., & Ratcliffe, R. G. (2005) · Photosynthesis Research · doi:10.1007/s11120-004-2081-8 · Cited by 69
“detecting coupling interactions ( Brown 2003 ).”
BackgroundShinyuy, L. M., Loe, G. E., Jansen, O., Mamede, L., Ledoux, A., Noukimi, S. F., Abenwie, S. N., Ghogomu, S. M., Souopgui, J., Robert, A. R., et al. (2023) · Metabolites · doi:10.3390/metabo13050613 · Cited by 58
Quantification of artemisinin in Artemisia annua extracts by 1H‐NMR
Castilho, P. C., Gouveia, S. C., & Rodrigues, A. I. (2008) · Phytochemical Analysis · doi:10.1002/pca.1053 · Cited by 48
Nuclear magnetic resonance spectroscopy in biosynthetic studies
Schneider, B. (2007) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2007.02.006 · Cited by 34
Synthesis of labelled dihydroartemisinic acid
Brown, G. D., & Sy, L.-K. (2004) · Tetrahedron · doi:10.1016/j.tet.2003.11.069 · Cited by 23
Self-citationLesot, P., Lafon, O., & Berdagué, P. (2014) · Magnetic Resonance in Chemistry · doi:10.1002/mrc.4118 · Cited by 20
Benzene at 1GHz. Magnetic field-induced fine structure
Heist, L. M., Poon, C., Samulski, E. T., Photinos, D. J., Jokisaari, J. P., Vaara, J., Emsley, J. W., Mamone, S., & Lelli, M. (2015) · Journal of Magnetic Resonance · doi:10.1016/j.jmr.2015.06.005 · Cited by 12
In vivo transformations of dihydro-epi-deoxyarteannuin B in Artemisia annua plants
Brown, G. D., & Sy, L. (2007) · Tetrahedron · doi:10.1016/j.tet.2007.06.016 · Cited by 8
Optimised NMR detection of 13C–2H double labelling in small molecules
Bartholomeusz, T. A., Mesnard, F., Felpin, F., Lebreton, J., Robins, R. J., & Roscher, A. (2005) · Comptes Rendus Chimie · doi:10.1016/j.crci.2005.06.026 · Cited by 4
Three Iridoid Glycosides from the Root Extract of Stachytarpheta Angustifolia Mill Vahl Verbenaceae
Mohammed, M. H. H., Bugaje, I. M., & Garba, M. A. (2015) · Journal of Chemistry and Biochemistry · doi:10.15640/jcb.v3n1a4 · Cited by 1
“The strong NOESY correlations between H – 1/H – 10 also indicated that, the linkage between C – 8 and C – 10 are in α orientation while the H – 10 is in β (Brown, 2003; Kemp, 1991).”
BackgroundSaponins from the Leaves of Cassia occidentalis (Caesalpiniaceae)
Mohammed, M., Adeyemi, M. M., Aboki, M. A., & Musa, S. H. (2013) · Cited by 1
Technology Development of NMR for Metabolic Analysis and Its Future Perspective
Kikuchi, J., Sekiyama, Y., & Date, Y. (2010) · RADIOISOTOPES · doi:10.3769/radioisotopes.59.637
Metadata
- Authors
- Brown, G. D.
- Affiliations
- University of Reading (GB)
- Corresponding author
- Brown, G.D.
- ORCID
- Brown, G.D.
- Venue
- Phytochemistry Reviews
- Published
- 2003-01
- Volume
- 2
- Issue
- 1-2
- Pages
- 45-59
- ISSN
- 1568-7767 (ISSN-L)
- 1572-980X
- OpenAlex
- W2089419525
- Cited by
- 16
- References
- 17
- Citations by year
- 2023: 1 · 2015: 2 · 2014: 1 · 2013: 1
- FWCI
- 0.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Phytochemistry Reviews (publishedVersion)
- Funders
- University Grants Committee
- University of Hong Kong
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
- Physical Sciences › Chemistry › Spectroscopy › Advanced NMR Techniques and Applications
- Physical Sciences › Chemistry › Organic Chemistry › Sesquiterpenes and Asteraceae Studies
- Keywords
- Artemisia annua, artemisinin biosynthesis, dihydroartemisinic acid, autoxidation
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