Total synthesis of (+)-pilosinine via a stereodivergent conjugate addition strategy-Reference-Cited by-同舟云学术

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Total synthesis of (+)-pilosinine via a stereodivergent conjugate addition strategy

Published:2020-06 Issue:23 Volume:61 Page:151945
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Schrank Cassandra L.,Danneman Michael W.,Prebihalo Emily A.,Anderson Robert E.,Gibson Tyler J.,Wuest William M.^ORCID,Mullins Richard J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. Conjugate Addition Reactions in Organic Synthesis; Tetrahedron Organic Chemistry Series;Perlmutter,1992

2. Asymmetric conjugate addition

3. Asymmetric 1,4-addition of organocuprates to chiral .alpha.,.beta.-unsaturated N-acyl-4-phenyl-2-oxazolidinones: a new approach to the synthesis of chiral .beta.-branched carboxylic acids

4. Diastereospecific tandem Michael-like addition / electrophilic bromination: A one-pot tandem asymmetric synthesis of precursors of unusual amino acids

5. Syntheses of highly constrained β-aryl isohexanoic acid derivatives via asymmetric Michael addition

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Time‐Dependent Diastereodivergent Michael Addition Enabled by Phosphazenes Acting as Catalysts and Reactants;Advanced Synthesis & Catalysis;2021-09-07

2. Asymmetric conjugate addition reactions with chiral oxadiazinones: Unusual conformational properties of the oxadiazinones;Tetrahedron;2021-03

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