A mechanistically designed mono-cinchona alkaloid is an excellent catalyst for the enantioselective dihydroxylation of olefins

Tetrahedron Letters

Volumn 35, Issue 35, 1994, Pages 6427-6430

  Corey, E J ^a   Noe, Mark C ^a   Grogan, Michael J ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1 DECENE; 1 PHENYLCYCLOHEXENE; 2 VINYLNAPHTHALENE; 3 HEXENE; CINCHONA ALKALOID; QUINIDINE DERIVATIVE; STILBENE; STYRENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CONFORMATIONAL TRANSITION; DRUG CONFORMATION; ENANTIOMER; HYDROXYLATION; REACTION ANALYSIS; STEREOCHEMISTRY;

CINCHONA;

EID: 0027967498     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78237-2     Document Type: Article

References (15)

1. X-Ray molecular structure of the asymmetrically bridged ester complex di-�-oxo-bis[(cyclohexane-1,2-diolato)oxo(quinuclidine)osmium(VI)], [OsO2(O2C6H10)(C7H13N)]2