A New Stereocontrolled Approach to a Key Intermediate in the Synthesis of (2S,3R)-Capreomycidine

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Title:A New Stereocontrolled Approach to a Key Intermediate in the Synthesis of (2S,3R)-Capreomycidine
Creators:
Martinková, Miroslava
Gonda, Jozef
Džoganová, Martina
Journal or Publication Title:
Collection of Czechoslovak Chemical Communications, 71, 8, pp. 1199-1210
Uncontrolled Keywords:Nonproteinogenic amino acids, [3,3]-Sigmatropic rearrangements, Capreomycins, Capreomycidine, Total synthesis, Stereoselectivity

Abstract

A new stereocontrolled approach to the synthesis of advanced intermediate in the synthesis of nonproteinogenic amino acid (2<i>S</i>,3<i>R</i>)-capreomycidine via the novel domino reaction has been developed. <p>

Title:A New Stereocontrolled Approach to a Key Intermediate in the Synthesis of (2S,3R)-Capreomycidine
Creators:
Martinková, Miroslava
Gonda, Jozef
Džoganová, Martina
Uncontrolled Keywords:Nonproteinogenic amino acids, [3,3]-Sigmatropic rearrangements, Capreomycins, Capreomycidine, Total synthesis, Stereoselectivity
Divisions:Life and Chemical Sciences > Institute of Organic Chemistry and Biochemistry > Collection of Czechoslovak Chemical Communications
Journal or Publication Title:Collection of Czechoslovak Chemical Communications
Volume:71
Number:8
Page Range:pp. 1199-1210
ISSN:0010-0765
E-ISSN:1212-6950
Publisher:Institute of Organic Chemistry and Biochemistry
Related URLs:
URLURL Type
http://dx.doi.org/10.1135/cccc20061199UNSPECIFIED
ID Code:2534
Item Type:Article
Deposited On:06 Feb 2009 17:19
Last Modified:06 Feb 2009 16:19

Citation

Martinková, Miroslava; Gonda, Jozef; Džoganová, Martina (2006) A New Stereocontrolled Approach to a Key Intermediate in the Synthesis of (2S,3R)-Capreomycidine. Collection of Czechoslovak Chemical Communications, 71 (8). pp. 1199-1210. ISSN 0010-0765

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