An Unusual Rearrangement of a LithiatedN-Acyl-tetrahydroisoquinoline to an Amino-indan Skeleton and Structural Comparison of 3-Amino-2-methylindan- and -tetrahydronaphthalene-2-carboxylic Acids as Possible Building Blocks for Peptide-Turn Mimics-Reference-Cited by-同舟云学术

An Unusual Rearrangement of a LithiatedN-Acyl-tetrahydroisoquinoline to an Amino-indan Skeleton and Structural Comparison of 3-Amino-2-methylindan- and -tetrahydronaphthalene-2-carboxylic Acids as Possible Building Blocks for Peptide-Turn Mimics

Published:1993-11-03 Issue:7 Volume:76 Page:2640-2653
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Gees Thomas,Schweizer W. Bernd,Seebach Dieter

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference45 articles.

1. Über isomere Bihydrocotarnine, ein Beitrag zur Stereochemie stickstoffhaltiger Verbindungen

2. Oxydative Aryl-Aryl-Verkn�pfung von 6,6?,7,7?-Tetramethoxy-1,1?,2,2?,3,3?,4,4?-octahydro-1,1?-biisochinolin-Derivaten

3. Alkylation of the isoquinoline skeleton in the 1-position

4. Lithiiertes N-Pivaloyl-tetrahydroisochinolin - ein Supernucleophil

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