Highly diastereoselective synthesis of fully substituted tetrahydrofurans by a one-pot cascade reaction of aryldiazoacetates with allyl alcohols

Chemistry - A European Journal

Volumn 15, Issue 46, 2009, Pages 12604-12607

  Xu, Xinfang ^a   Han, Xingchun ^a,b   Yang, Liping ^a   Hu, Wenhao ^a,c  

^a EAST CHINA NORMAL UNIVERSITY   (China)

^b Roche China Ltd   (China)

^c NANKAI UNIVERSITY   (China)

Author keywords

Diastereoselectivity; Domino reactions; Michael addition; O H insertion; Tetrahydrofurans

Indexed keywords

DIASTEREO-SELECTIVITY; DOMINO REACTIONS; MICHAEL ADDITIONS; O-H INSERTION; TETRAHYDROFURANS;

ENANTIOSELECTIVITY; ORGANIC POLYMERS; REACTION KINETICS; RHODIUM; STEREOSELECTIVITY; SUBSTITUTION REACTIONS; TOLUENE;

ADDITION REACTIONS;

ACETIC ACID DERIVATIVE; ALLYL ALCOHOL; FURAN DERIVATIVE; PROPANOL; TETRAHYDROFURAN;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; ENZYME SPECIFICITY; STEREOISOMERISM; SYNTHESIS;

ACETATES; FURANS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PROPANOLS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 71549167604     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200902093     Document Type: Article

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