Bifunctional thiourea-catalyzed enantioselective double Michael reaction of γ,δ-unsaturated β-ketoester to nitroalkene: asymmetric synthesis of (−)-epibatidine-Reference-Cited by-同舟云学术

Bifunctional thiourea-catalyzed enantioselective double Michael reaction of γ,δ-unsaturated β-ketoester to nitroalkene: asymmetric synthesis of (−)-epibatidine

Published:2004-12 Issue:50 Volume:45 Page:9185-9188
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hoashi Yasutaka,Yabuta Takaya,Takemoto Yoshiji

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference72 articles.

1. Diastereo- and Enantioselective Catalytic Carbometallative Aldol Cycloreduction: Tandem Conjugate Addition−Aldol Cyclization

2. Catalytic Enantioselective Synthesis of (−)-Prostaglandin E1 Methyl Ester Based on a Tandem 1,4-Addition−Aldol Reaction

3. Tandem Asymmetric Conjugate Addition−Silylation of Enantiomerically Enriched Zinc Enolates. Synthetic Importance and Mechanistic Implications

4. An Asymmetric Cyanation Reaction and Sequential Asymmetric Cyanation–Nitroaldol Reaction Using a [YLi3{tris(binaphthoxide)}] Single Catalyst Component: Catalyst Tuning with Achiral Additives

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