Direct syntheses of spiro- and fused-hydrofurans by a tunable tandem semipinacol rearrangement/oxa-michael addition protocol

Chemistry - A European Journal

Volumn 19, Issue 17, 2013, Pages 5246-5249

  Li, Bao Sheng ^a   Liu, Wen Xing ^a   Zhang, Qing Wei ^a   Wang, Shao Hua ^a   Zhang, Fu Min ^a   Zhang, Shu Yu ^a   Tu, Yong Qiang ^a   Cao, Xiao Ping ^a  

^a LANZHOU UNIVERSITY   (China)

Author keywords

chemoselectivity; dihydrofurans; Michael addition; semipinacol rearrangements; tandem reactions

Indexed keywords

CHEMO-SELECTIVITY; DIHYDROFURANS; MICHAEL ADDITIONS; SEMIPINACOL REARRANGEMENTS; TANDEM REACTION;

REACTION INTERMEDIATES;

ADDITION REACTIONS;

CYCLOHEXENE DERIVATIVE; FURAN DERIVATIVE; SEMIPINACOL; SPIRO COMPOUND;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

CYCLOHEXENES; FURANS; MOLECULAR STRUCTURE; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84876252109     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201300205     Document Type: Article

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