Cyclic imidate salts in acyclic stereochemistry: Diastereoselective syn-epoxidation of 2-alkyl-4-enamides to epoxyamides-Reference-Cited by-同舟云学术

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Cyclic imidate salts in acyclic stereochemistry: Diastereoselective syn-epoxidation of 2-alkyl-4-enamides to epoxyamides

Published:1996-02 Issue:9 Volume:52 Page:3327-3338
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Maligres P.E.,Weissman S.A.,Upadhyay V.,Cianciosi S.J.,Reamer R.A.,Purick R.M.,Sager J.,Rossen K.,Eng K.K.,Askin D.,Volante R.P.,Reider P.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. 1,3-Asymmetric induction: highly stereoselective synthesis of 2,4-trans-disubstituted γ-butyrolactones and γ-butyrothiolactones

2. Preparation of Nonracemic 3,5-Disubstituted-.gamma.-butyrolactones: An Effective Sequent Auxiliary for Amide Alkylation and Iodolactonization

3. Enantioselective halolactonisation of bis-γ,δ-unsaturated carboxylic acid derivatives: use of a sultam and oxazolidine-2-ones as chiral auxiliary

4. Highly enantioselective creation of quaternary carbons in a halolactonization of bis-γ,δ-unsaturated carboxylic imides derived from a camphorsultam: Enantioselective synthesis of (+)-mesembrine

5. Chiral Route to Some Alkaloids through Asymmetric Iodolactonization

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4. Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals;Organic Process Research & Development;2016-02-05

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