Highly enantioselective synthesis of α-trichloromethyldihydropyrans catalyzed by bifunctional organocatalysts

Tetrahedron

Volumn 67, Issue 10, 2011, Pages 1774-1780

  Wang, Hai Feng ^a   Li, Peng ^a   Cui, Hai Feng ^a   Wang, Xiao Wei ^a   Zhang, Jun Kang ^a   Liu, Wen ^b   Zhao, Gang ^a,b  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA   (China)

Author keywords

Bifunctional organocatalysts; Dihydropyrans; Enantioselectivity; Michael addition; Trichloromethyl ketones

Indexed keywords

ALPHA TRICHLOROMETHYLDIHYDROPYRAN DERIVATIVE; CINCHONA ALKALOID; CYANOKETONE; KETONE DERIVATIVE; PHENYLALANINE; PIPERAZINE; PYRAN DERIVATIVE; THIOUREA; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CHIRALITY; DRUG SYNTHESIS; ENANTIOSELECTIVITY; MICHAEL ADDITION; PRIORITY JOURNAL; REACTION OPTIMIZATION; SCREENING; STEREOCHEMISTRY;

EID: 79951649315     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.01.043     Document Type: Article

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