Highly stereoselective Michael reduction/intramolecular Michael reaction cascade to synthesize trans-stereodiad comprising an all-carbon quaternary stereogenic center-Reference-Cited by-同舟云学术

Highly stereoselective Michael reduction/intramolecular Michael reaction cascade to synthesize trans-stereodiad comprising an all-carbon quaternary stereogenic center

Published:2014-01 Issue:5 Volume:55 Page:1100-1103
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujii Tomohiro,Orimoto Kohei,Nakada Masahisa

Funder

Waseda University

Scientific Research on Innovative Areas ‘Organic Synthesis based on Reaction Integration, Development of New Methods and Creation of New Substances’

Excellent Graduate Schools (Practical Chemical Wisdom), MEXT, Japan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. Tumor inhibitors. 100. Isolation and structural elucidation of bruceantin and bruceantinol, new potent antileukemic quassinoids from Brucea antidysenterica

2. Catalytic Asymmetric [4 + 2] Cycloadditions and Hosomi–Sakurai Reactions of α-Alkylidene β-Keto Imides

3. Li(sec-Bu)3BH-Mediated Cyclohexane Annulation of 2,7-Nonadienedioic Diesters

4. Stereoselective synthesis of (−)-gabosine C using a Nozaki–Hiyama–Kishi reaction and RCM

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