Stereoselectivity in the rhodium(II) acetate catalysed cyclopropanations of 2-diazo-1-indanone with styrenes

Tetrahedron Letters

Volumn 41, Issue 10, 2000, Pages 1491-1494

  Bauta, William ^a   Dodd, John ^a   Bullington, James ^a   Gauthier, Diane ^b   Leo, Gregory ^b   McDonnell, Patricia ^b  

^a Drug Discovery Raritan   (United States)

^b JOHNSON AND JOHNSON PHARMACEUTICAL RESEARCH AND DEVELOPMENT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; CYCLOPROPANE; INDANONE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; RHODIUM COMPLEX; STYRENE DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; DIASTEREOISOMER; ELECTRON; ISOMER; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0034603591     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)00002-2     Document Type: Article

References (14)

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12. Shechter and co-workers have reported the rhodium acetate catalysed reaction of 4 with styrene in toluene from which they isolated a single cyclopropane of undetermined stereochemistry in 59% yield. Rosenfeld, M. J.; Ravi Shankar, B. K.; Schechter, H. J. Org. Chem. 1988, 53, 2699.
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