α-hydroxy esters as inexpensive chiral auxiliaries in rhodium(II)-catalyzed cyclopropanations with vinyldiazomethanes

Tetrahedron Letters

Volumn 32, Issue 45, 1991, Pages 6509-6512

  Davies, Huw M L ^a   Cantrell Jr , William R ^a  

^a WAKE FOREST UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; PRIORITY JOURNAL; REACTION ANALYSIS; SYNTHESIS;

EID: 0025990243     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(91)80206-L     Document Type: Article

References (26)

1. Semicorrin metal complexes as enantioselective catalysts. Part 2. Enantioselective cyclopropane formation from olefins with diazo compounds catalyzed by chiral (semicorrinato)copper complexes
2. Asymmetric synthesis in carbon?carbon bond forming reactions of ?-diazoketones catalysed by homochiral rhodium(II) carboxylates
3. The thermal chemistry of vinyldiazo compounds as a method for the generation of vinylmethylenes
4. Enantioselective ring construction with control of side-chain stereochemistry. Synthesis of (+)-isoneonepetalactone
5. Enantioselective Synthesis of (R)-N-Boc-1-amino-2-arylcyclopropene-1-carboxylic Acid Methyl Ester