Diastereoselectivity in the OH insertion reactions of rhodium carbenoids derived from phenyldiazoacetates of homochiral alcohols

Tetrahedron Letters

Volumn 35, Issue 32, 1994, Pages 5949-5952

  Aller, Enrique ^a   Cox, Geoffrey G ^a   Miller, David J ^a   Moody, Christopher J ^a  

^a LOUGHBOROUGH UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

2 PHENYLCYCLOHEXANOL; 2 PROPANOL; 8 PHENYLMENTHOL; ALCOHOL DERIVATIVE; METHANOL; PHENYLDIAZOACETATE DERIVATIVE; RHODIUM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DIASTEREOISOMER; DRUG DEGRADATION; DRUG STRUCTURE; DRUG SYNTHESIS; MOLECULAR INTERACTION;

EID: 0027978020     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78227-X     Document Type: Article

References (15)

1. Transition-metal catalyzed decomposition of aliphatic diazo compounds — New results and applications in organic synthesis
2. Rhodium(II) Trifluoroacetamide; an Excellent Catalyst for Carbenoid O-H Insertion Reactions
3. Diastereoselectivity Enhancement in Cyclopropanation and Cyclopropenation Reactions of Chiral Diazoacetate Esters Catalyzed by Chiral Dirhodium(II) Carboxamides
4. Diastereoselective reduction of an α-keto-ester derived from (−)-8-phenylmenthol: A 4-step synthesis of R-Halostachine analogue.