An aza-Payne rearrangement-epoxide ring opening reaction of 2-aziridinemethanols in a one-pot manner: A regio- and stereoselective synthetic route to diastereomerically pure N-protected 1,2-amino alcohols-Reference-Cited by-同舟云学术

An aza-Payne rearrangement-epoxide ring opening reaction of 2-aziridinemethanols in a one-pot manner: A regio- and stereoselective synthetic route to diastereomerically pure N-protected 1,2-amino alcohols

Published:1996-09 Issue:36 Volume:52 Page:11739-11752
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ibuka Toshiro,Nakai Kazuo,Akaji Masako,Tamamura Hirokazu,Fujii Nobutaka,Yamamoto Yoshinori

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference56 articles.

1. Convenient Asymmetric Syntheses of anti-β-Amino Alcohols

2. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

3. Ready access to stereodefined β-hydroxy-γ-amino acids. Enantioselective synthesis of fully protected cyclohexylstatine

4. An improved, convenient procedure for reduction of amino acids to aminoalcohols: Use of NaBH4-H2SO4

5. A convenient reduction of amino acids and their derivatives

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