The highly enantiocontrolled functionalization of a 2-oxazolone heterocycle by intramolecular radical-based addition. A chiral synthon for 2-amino alcohols which contain three contiguous stereocenters-Reference-Cited by-同舟云学术

The highly enantiocontrolled functionalization of a 2-oxazolone heterocycle by intramolecular radical-based addition. A chiral synthon for 2-amino alcohols which contain three contiguous stereocenters

Published:1998-09 Issue:39 Volume:39 Page:7131-7134
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Morita Toru,Matsunaga Hirofumi,Sugiyama Eiji,Ishizuka Tadao,Kunieda Takehisa

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Versatile chiral synthons for vic-amino alcohols. Facile synthesis of (2S,3R)-3-hydroxyglutamic acid and (+)-statine

2. Chiral synthons for 2-amino alcohols. Facile preparation of optically active amino hydroxy acids of biological interest.

3. Lewis acid-promoted direct substitution of 4-methoxy- and 4-phenylthio-2-oxazolidinones by alkyl cuprates. Facile preparation of (3s,4s)-statine and (3s,4s)-cyclohexylstatine.

4. Facile Synthesis of (2S,3R)-3-Amino-2-Hydroxycarboxylic Acids, the Key Components of Amastatin and Bestatin

5. Stereoselective Synthesis of (−)-α-Kainic Acid and (+)-α-Allokainic Acid via Trimethylstannyl-Mediated Radical Carbocyclization and Oxidative Destannylation

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1. ChemInform Abstract: The Highly Enantiocontrolled Functionalization of a 2-Oxazolone Heterocycle by Intramolecular Radical-Based Addition. A Chiral Synthon for 2-Amino Alcohols which Contain Three Contiguous Stereocenters.;ChemInform;2010-06-18

2. Synthetic Uses of R3MH (MÂ =Â Ge, Sn, Pb);PATAI'S Chemistry of Functional Groups;2009-12-15

3. Recent Advances in Stereoselective Syntheses Using N-Acylimines;Synthesis;2007-01

4. Synthetic utility of five-membered heterocycles—chiral functionalization and applications;Tetrahedron;2005-08

5. One or More CH Bond(s) Formed by Substitution: Reduction of CHalogen and CChalcogen Bonds;Comprehensive Organic Functional Group Transformations II;2005