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  AMINO-ACID ESTERS - VERSATILE CHIRAL AUXILIARY GROUPS FOR THE ASYMMETRIC-SYNTHESIS OF NITROGEN-HETEROCYCLES

Waldmann, H. (1995). AMINO-ACID ESTERS - VERSATILE CHIRAL AUXILIARY GROUPS FOR THE ASYMMETRIC-SYNTHESIS OF NITROGEN-HETEROCYCLES. SYNLETT, (2), 133-141.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-729E-1 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-9A7F-9
Genre: Journal Article

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 Creators:
Waldmann, Herbert1, Author           
Affiliations:
1Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

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Free keywords: DIELS-ALDER REACTIONS; MANNICH-MICHAEL REACTIONS; (S)-PROLINE BENZYL ESTER; YOHIMBINE-TYPE ALKALOIDS; BARBIER-TYPE REACTIONS; AQUEOUS-SOLUTION; BRASSARD-DIENE; IMINIUM SALTS; IMINES; INDOLYLETHYLIMINES
 Abstract: The development of amino acid esters as chiral auxiliary groups for the asymmetric construction of N-heterocycles by means of aza Diels-Alder reactions, Mannich reactions, Pictet-Spengler reactions and 1,3-dipolar cycloadditions is described. Also their application in the steric steering of carbo Diels-Alder reactions, radicalic transformations and enantioselective nucleophilic additions to carbonyl groups is highlighted.

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Language(s): eng - English
 Dates: 1995-02
 Publication Status: Issued
 Pages: 9
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: A1995QG63100002
 Degree: -

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Title: SYNLETT
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: STUTTGART : GEORG THIEME VERLAG
Pages: - Volume / Issue: (2) Sequence Number: - Start / End Page: 133 - 141 Identifier: ISSN: 0936-5214