Enantioselective synthesis of functionalized 2-amino-4H-chromenes via the o-quinone methides generated from 2-(1-tosylalkyl)phenols

Tetrahedron Letters

Volumn 56, Issue 29, 2015, Pages 4334-4338

  Wu, Bo ^a   Gao, Xiang ^a   Yan, Zhong ^a   Huang, Wen Xue ^a   Zhou, Yong Gui ^a,b  

^a DALIAN INSTITUTE OF CHEMICAL PHYSICS   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

2 (1 Tosylalkyl)phenols; 2 Amino 4H chromenes; o Quinone methides

Indexed keywords

2 (1 TOSYLALKYL)NAPHTHOL; 2 (1 TOSYLALKYL)PHENOL DERIVATIVE; 2 AMINO 4H CHROMENE DERIVATIVE; CARBENE; CHROMENE DERIVATIVE; MALONONITRILE; PHENOL DERIVATIVE; QUINONE DERIVATIVE; QUINONE METHIDE DERIVATIVE; THIOUREA; UNCLASSIFIED DRUG;

AMINATION; ARTICLE; CRYSTAL STRUCTURE; ENANTIOSELECTIVITY; MICHAEL ADDITION; SYNTHESIS; TEMPERATURE;

EID: 84930925764     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2015.05.076     Document Type: Article

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