The first example of a diastereoselective thio-Ugi reaction: A new synthetic approach to chiral imidazole derivatives

Journal of Organic Chemistry

Volumn 72, Issue 21, 2007, Pages 7878-7885

  Gulevich, Anton V ^a   Balenkova, Elizabeth S ^a   Nenajdenko, Valentine G ^a  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOMERS; DIASTEREOSELECTIVE; THIO-UGI REACTION; THIOAMIDES;

AMIDES; AMINES; ENZYME INHIBITION; HYDROCHLORIC ACID; ISOMERS; SYNTHESIS (CHEMICAL);

STEREOSELECTIVITY;

ALPHA METHYLBENZYLAMINE; AMIDINE; AMMONIA; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; HYDROCHLORIC ACID; IMIDAZOLE DERIVATIVE; PROTEINASE INHIBITOR; SB 203386; THIOAMIDE; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; CHEMICAL REACTION; CHIRALITY; CYCLIZATION; DIASTEREOISOMER; ISOMER; QUANTUM YIELD; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS; THIO UGI REACTION;

CHEMISTRY, ORGANIC; CHEMISTRY, PHARMACEUTICAL; IMIDAZOLES; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 35348870997     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo071030o     Document Type: Article

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