Hydrogen-bond-promoted palladium catalysis: Allylic alkylation of indoles with unsymmetrical 1,3-disubstituted allyl acetates using chiral bis(sulfoxide) phosphine ligands

Angewandte Chemie - International Edition

Volumn 52, Issue 15, 2013, Pages 4207-4211

  Du, Le ^a,b,c   Cao, Peng ^a,b   Xing, Junwei ^a,b,c   Lou, Yazhou ^a,b   Jiang, Liyin ^a,b   Li, Liangchun ^a,b,c   Liao, Jian ^a,b,d  

^a CHENGDU INSTITUTE OF BIOLOGY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c CHENGDU INSTITUTE OF ORGANIC CHEMISTRY   (China)

^d SICHUAN UNIVERSITY   (China)

Author keywords

allylic compounds; hydrogen bonds; kinetic resolution; ligand design; palladium

Indexed keywords

ALLYLIC ALKYLATION; ALLYLIC COMPOUNDS; ASYMMETRIC ALLYLIC ALKYLATIONS; DYNAMIC KINETIC ASYMMETRIC TRANSFORMATIONS; KINETIC RESOLUTION; LIGAND DESIGN; PALLADIUM CATALYSIS; PALLADIUM-CATALYZED;

ALLYLATION; CATALYSIS; FUNCTIONAL GROUPS; HYDROGEN BONDS; ORGANOMETALLICS; PALLADIUM; PHOSPHORUS COMPOUNDS;

LIGANDS;

ACETIC ACID DERIVATIVE; ALLYL COMPOUND; INDOLE DERIVATIVE; LIGAND; ORGANOMETALLIC COMPOUND; PALLADIUM; PHOSPHINE DERIVATIVE; SULFOXIDE;

ALKYLATION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; HYDROGEN BOND; SYNTHESIS;

ACETATES; ALKYLATION; ALLYL COMPOUNDS; CATALYSIS; HYDROGEN BONDING; INDOLES; LIGANDS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; PALLADIUM; PHOSPHINES; SULFOXIDES;

EID: 84875827782     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201209485     Document Type: Article

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