Sulfanyl-methylene-5(4H)-oxazolones and β-sulfanyl-α-nitroacrylates as appealing dienophiles for the synthesis of conformationally constrained cysteine analogues-Reference-Cited by-同舟云学术

Sulfanyl-methylene-5(4H)-oxazolones and β-sulfanyl-α-nitroacrylates as appealing dienophiles for the synthesis of conformationally constrained cysteine analogues

Published:2012-02 Issue:7 Volume:68 Page:1951-1962
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ruffoni Alessandro,Casoni Alessandro,Pellegrino Sara,Gelmi Maria Luisa,Soave Raffaella,Clerici Francesca

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

1. A Highly Diastereoselective Approach to Conformationally Constrained Serine Analogues: Synthesis of an α-Amino-β-hydroxycyclohexenecarboxylic Acid and Derivatives

2. Conformationally Constrained Serine Analogues: Synthesis of New 2-Amino-3-hydroxynorbornanecarboxylic Acid Derivatives

3. Carbocyclic serine analogues: regio- and diastereoselective syntheses of new 1-amino-2,5-dihydroxycyclohexanecarboxylic acids

4. A Highly Diastereoselective Synthesis of New Polyhydroxy 2-Aminonorbornanecarboxylic Acids

5. Asymmetric Synthesis of 2-Amino-3-hydroxynorbornene-2-carboxylic Acid Derivatives

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