Enantioselective synthesis of (+)-indolizidine, (+)-laburnine and (+)-elaeokanines A and C using the Diels–Alder reaction of α-(2-exo-hydroxy-10-bornylsulfinyl)maleimide-Reference-Cited by-同舟云学术

Enantioselective synthesis of (+)-indolizidine, (+)-laburnine and (+)-elaeokanines A and C using the Diels–Alder reaction of α-(2-exo-hydroxy-10-bornylsulfinyl)maleimide

Published:1994 Issue:1 Volume: Page:15-23
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Arai Yoshitsugu,Kontani Tohru,Koizumi Toru

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1994/P1/P19940000015

Reference46 articles.

1. Y. Arai , M.Matsui, A.Fujii, T.Kontani, T.Ohno, T.Koizumi and M.Shiro, preceding paper.

2. Stereocontrol in intermolecular nucleophilic addition to N-acyliminium ion directed by a bicyclo(2.2.1)heptene or 7-oxabicyclo(2.2.1)heptene group. A novel route to 5-substituted 3-pyrrolin-2-ones of high optical purity.

3. Synthesis of (+)-elaeokanine A and (+)-elaeokanine C based upon a novel approach involving diastereoselective, nucleophilic addition to N-acyliminium ion and retro Diels-Alder reaction

4. Ueber die Coniceïne

5. Ueber die Coniceïne

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