Indole alkaloids. A combined chemical and enzymatic route for eburnane ring construction : Formal synthesis of (−)-Eburnamonine
- 1 January 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (31) , 9487-9494
- https://doi.org/10.1016/s0040-4020(01)85522-8
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Asymmetric creation of quaternary carbon centersChemical Reviews, 1993
- Stereoselective alkylation of dianions derived from chiral half-esters of monosubstituted malonic acids: asymmetric synthesis of α-alkyl α-amino acids and key synthetic intermediates for Hunteria and Aspidosperma indole alkaloidsJournal of the Chemical Society, Perkin Transactions 1, 1991
- An Asymmetric Synthesis of the Takano Lactone. A Formal Synthesis of 9-(—)-EburnamineHETEROCYCLES, 1990
- Chiral total synthesis of indole alkaloids of the Aspidosperma and Hunteria typesThe Journal of Organic Chemistry, 1990
- The Hetero-Cope Rearrangement in Organic SynthesisSynthesis, 1989
- The thermal, aliphatic Claisen rearrangementChemical Reviews, 1988
- Chiral synthesis of (+)-eburnamine, (–)-eburnamenine, and (–)-eburnamonineJournal of the Chemical Society, Perkin Transactions 1, 1985
- Methodology for the construction of quaternary carbon centersTetrahedron, 1980
- Lanthanides in organic chemistry. 1. Selective 1,2 reductions of conjugated ketonesJournal of the American Chemical Society, 1978
- Syntheses with Dihydroresorcinol Mono Ethyl Ether: 3-Alkyl-Δ2-cyclohexenonesJournal of the American Chemical Society, 1949