A facile asymmetric synthesis of either enantiomer of 2-substituted pyrrolidines

Journal of Organic Chemistry

Volumn 75, Issue 7, 2010, Pages 2236-2246

  Reddy, Leleti Rajender ^a   Das, Sonia G ^b   Liu, Yugang ^a   Prashad, Mahavir ^a  

^a NOVARTIS PHARMA AG   (Switzerland)

^b UNIVERSITY OF MINNESOTA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALIPHATIC SUBSTITUENTS; ASYMMETRIC SYNTHESIS; DEPROTECTION; DIASTEREO-SELECTIVITY; EPIMERS; GENERAL METHOD; GOOD YIELD; KETIMINES; PYRROLIDINES; REDUCTIVE CYCLIZATION; STARTING MATERIALS;

CHIRALITY; CYCLIZATION; ELECTRON TRANSITIONS; ENANTIOMERS; ETHERS; STEREOSELECTIVITY; TOLUENE;

SYNTHESIS (CHEMICAL);

CHLORIDE; DIOXANE; IMINE; LITHIUM DERIVATIVE; METHANOL; PIPERIDINE DERIVATIVE; PYRROLIDINE DERIVATIVE; REDUCING AGENT; TOLUENE;

ARTICLE; ASYMMETRIC SYNTHESIS; CYCLIZATION; DEPROTECTION REACTION; ENANTIOMER; EPIMER; METHODOLOGY; STEREOCHEMISTRY;

CROSS-LINKING REAGENTS; CYCLIZATION; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PYRROLIDINES; STEREOISOMERISM;

EID: 77950320555     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo902710s     Document Type: Article

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