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  4. Synthesis of diastereomers of complestatin and chloropeptin I: substrate-dependent atropstereoselectivity of the intramolecular Suzuki-Miyaura reaction
 
research article

Synthesis of diastereomers of complestatin and chloropeptin I: substrate-dependent atropstereoselectivity of the intramolecular Suzuki-Miyaura reaction

Jia, Yanxing
•
Bois-Choussy, Michele
•
Zhu, Jieping  
2008
Angewandte Chemie International Edition

Atropisomers as well as CC2 epimers of complestatin and chloropeptin I are readily synthesized through an intramol. SNAr reaction and the Suzuki-Miyaura reaction. The abs. configuration of amino acid N-methyl-2-(3,5-dichloro-4-hydroxyphenyl)glycine was found to det. the atropselectivity of the aryl-aryl bond-forming reaction. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1002/anie.200800599
Author(s)
Jia, Yanxing
Bois-Choussy, Michele
Zhu, Jieping  
Date Issued

2008

Publisher

Wiley-VCH Verlag GmbH

Published in
Angewandte Chemie International Edition
Volume

47

Issue

22

Start page

4167

End page

4172

Subjects

Suzuki coupling reaction (-Miyaura

•

intramol.; total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); Substitution reaction (arom.

•

intramol.; total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); Macrocyclic compounds Role: SPN (Synthetic preparation)

•

PREP (Preparation) (peptidyl-; total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); Atropisomers; Chirality; Stereoselective synthesis (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); Peptides Role: RCT (Reactant)

•

SPN (Synthetic preparation)

•

PREP (Preparation)

•

RACT (Reactant or reagent) (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step)

•

complestatin chloropeptin diastereomer macrocycle atropisomer prepn Suzuki Miyaura reaction

Note

CAN 149:224538

34-3

Amino Acids, Peptides, and Proteins

Institut de Chimie des Substances Naturelles,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

72287-26-4 Role: CAT (Catalyst use), USES (Uses) (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); 69598-75-0 (Complestatin); 160219-64-7 (Chloropeptin I) Role: MSC (Miscellaneous) (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); 1042907-15-2P Role: PRP (Properties), RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); 26973-43-3; 57591-61-4; 400778-04-3; 854443-88-2; 1042907-14-1; 1042907-16-3; 1042907-29-8; 1042907-31-2; 1042907-34-5; 1043894-16-1; 1143947-61-8 Role: RCT (Reactant), RACT (Reactant or reagent) (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); 586413-55-0P; 586413-73-2P; 854443-92-8P; 1042907-17-4P; 1042907-18-5P; 1042907-19-6P; 1042907-20-9P; 1042907-21-0P; 1042907-22-1P; 1042907-23-2P; 1042907-24-3P; 1042907-25-4P; 1042907-26-5P; 1042907-27-6P; 1042907-28-7P; 1042907-30-1P; 1042907-32-3P; 1042907-33-4P; 1042907-35-6P; 1043894-01-4P; 1043894-03-6P; 1043894-05-8P; 1043894-07-0P; 1043894-09-2P; 1043894-15-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step); 854613-13-1P; 1043893-99-7P; 1043894-11-6P; 1043894-13-8P; 1043902-22-2P (Epi-AA-Cc2-complestatin methyl ester); 1043902-24-4P (Epi-AA-Cc2-isochloropeptin methyl ester) Role: SPN (Synthetic preparation), PREP (Preparation) (total synthesis of diastereomers of complestatin and chloropeptin with atropstereoselective intramol. Suzuki-Miyaura reaction as a key step)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58416
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