The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.
Organocatalytic Asymmetric Domino Knoevenagel/Diels–Alder Reactions: A Bioorganic Approach to the Diastereospecific and Enantioselective Construction of Highly Substituted Spiro[5,5]undecane‐1,5,9‐triones
Abstract
A practical and environmentally friendly organocatalytic process for the synthesis of optically active highly substituted spiro[5,5]undecane-1,5,9-triones was achieved through the reaction of an aldehyde, an enone, and Meldrum's acid in the presence of a catalytic amount of chiral amino acid (see scheme). The Diels–Alder products were obtained as single diastereomers in excellent yields and enantiomeric excesses.
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Citations
Cites
Domino Reactions in Organic Synthesis
Tietze, L. F. (1996) · Chemical Reviews · doi:10.1021/cr950027e · Cited by 3,923
Proline-Catalyzed Direct Asymmetric Aldol Reactions
List, B., Lerner, R. A., & Barbas, C. F. (2000) · Journal of the American Chemical Society · doi:10.1021/ja994280y · Cited by 2,873
Self-citationSequential Transformations in Organic Chemistry: A Synthetic Strategy with a Future
Tietze, L. F., & Beifuss, U. (1993) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199301313 · Cited by 1,379
Asymmetric synthesis of bicyclic intermediates of natural product chemistry
Hajos, Z. G., & Parrish, D. R. (1974) · The Journal of Organic Chemistry · doi:10.1021/jo00925a003 · Cited by 1,252
Sakthivel, K., Notz, W., Bui, T., & Barbas, C. F. (2001) · Journal of the American Chemical Society · doi:10.1021/ja010037z · Cited by 1,166
Self-citationNew Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures
Eder, U., Sauer, G., & Wiechert, R. (1971) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197104961 · Cited by 1,057
The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes
Northrup, A. B., & MacMillan, D. W. C. (2002) · Journal of the American Chemical Society · doi:10.1021/ja0262378 · Cited by 706
Sequentielle Transformationen in der Organischen Chemie eine Synthesestrategie mit Zukunft
Tietze, L. F., & Beifuss, U. (1993) · Angewandte Chemie · doi:10.1002/ange.19931050204 · Cited by 558
H-Bonding Additives Act Like Lewis Acid Catalysts
Schreiner, P. R., & Wittkopp, A. (2002) · Organic Letters · doi:10.1021/ol017117s · Cited by 475
A Highly Enantioselective Amino Acid-Catalyzed Route to Functionalized α-Amino Acids
Córdova, A., Notz, W., Zhong, G., Betancort, J. M., & Barbas, C. F. (2002) · Journal of the American Chemical Society · doi:10.1021/ja017270h · Cited by 425
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Cited by
Asymmetric Aminocatalysis—Gold Rush in Organic Chemistry
Melchiorre, P., Marigo, M., Carlone, A., & Bartoli, G. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200705523 · Cited by 1,256
Asymmetric Organocatalysis: From Infancy to Adolescence
Dondoni, A., & Massi, A. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200704684 · Cited by 1,252
Organocatalysis Lost: Modern Chemistry, Ancient Chemistry, and an Unseen Biosynthetic Apparatus
Barbas, C. F. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200702210 · Cited by 527
Self-citationBencivenni, G., Wu, L., Mazzanti, A., Giannichi, B., Pesciaioli, F., Song, M., Bartoli, G., & Melchiorre, P. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200903192 · Cited by 448
Asymmetrische Organokatalyse: Eintritt in die Reifezeit
Dondoni, A., & Massi, A. (2008) · Angewandte Chemie · doi:10.1002/ange.200704684 · Cited by 398
Metadata
- Authors
- Ramachary, D. B., Chowdari, N. S., & Barbas, C. F.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2003-09-15
- Volume
- 42
- Issue
- 35
- Pages
- 4233-4237
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2099465025
- Cited by
- 375
- References
- 13
- FWCI
- 10.80
- Type
- journal article
- Language
- en
- Open access
- closed
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- Ramachary, D. B., Chowdari, N. S., & Barbas, C. F. (2003). Organocatalytic Asymmetric Domino Knoevenagel/Diels–Alder Reactions: A Bioorganic Approach to the Diastereospecific and Enantioselective Construction of Highly Substituted Spiro[5,5]undecane‐1,5,9‐triones. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200351916
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