Sulfoxide-mediated diastereoselective Michael additions. New enantioselective synthesis of C-4 substituted 2-pyroaminoadipic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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Cited by 9 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. ChemInform Abstract: Sulfoxide-Mediated Diastereoselective Michael Additions. New Enantioselective Synthesis of C-4 Substituted 2-Pyroaminoadipic Acids.;ChemInform;2010-06-13
2. Total diastereoselectivity in the one-pot multistep reaction of (RS)-(+)-{[(4-methylphenyl)sulfinyl]methyl}-1-oxa-4-azaspiro[4.5]dec-3-ene and E-methyl cinnamate. An approach to (2S,4S,5R,6R)-2-(hydroxymethyl)-4,6-diphenyl-1-azabicycle[3.3.1]nonane;Tetrahedron: Asymmetry;2008-06
3. A new approach to vinyl glycine derivatives from (+)-(RS)-3-[(p-toluenesulfinyl)methyl]-1-oxa-4-azaspiro[4,5]decen-3-ene;Tetrahedron: Asymmetry;2004-11
4. 1-Azaallylic Anions in Heterocyclic Chemistry;Chemical Reviews;2004-04-17
5. Recent developments in chiral non-racemic sulfinyl group chemistry in asymmetric synthesis;Arkivoc;2003-07-07
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