Applications of Baylis-Hillman chemistry: Enantioselective synthesis of (-)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy

Tetrahedron

Volumn 57, Issue 38, 2001, Pages 8167-8172

  Basavaiah, Deevi ^a   Kumaragurubaran, Nagaswamy ^a   Sharada, Duddu S ^a   Reddy, Ravi Mallikarjuna ^a  

^a UNIVERSITY OF HYDERABAD   (India)

Author keywords

Baylis Hillman chemistry; Chiral leaving group; Methyl 3 aryl 2 methylene 3 (prop 2 yn 1 yloxy)propanoates

Indexed keywords

ALCOHOL DERIVATIVE; ALLYL COMPOUND; BROMINE DERIVATIVE; METHYL 2 METHYLENE 3 (2 METHYLPHENYL) 3 (PROP 2 YN 1 YLOXY)PROPANOATE; METHYL 2 METHYLENE 3 (4 METHYLPHENYL) 3 (PROP 2 YN 1 YLOXY)PROPANOATE; METHYL 2 METHYLENE 3 (PROP 2 YN 1 YLOXY) 3 PHENYLPROPANOATE; METHYL 3 (4 CHLOROPHENYL) 2 METHYLENE 3 (PROP 2 YN 1 YLOXY)PROPANOATE; METHYL 3 (4 ETHYLPHENYL) 2 METHYLENE 3 (PROP 2 YN 1 YLOXY)PROPANOATE; METHYL 3 (4 ISOPROPYLPHENYL) 2 METHYLENE 3 (PROP 2 YN 1 YLOXY)PROPANOATE; PROPIONIC ACID DERIVATIVE; QUINIDINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHIRALITY; ENANTIOMER; METHODOLOGY; ORGANIC CHEMISTRY; PRIORITY JOURNAL; REACTION ANALYSIS; STOICHIOMETRY; SYNTHESIS;

EID: 0035903871     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)00786-4     Document Type: Article

References (31)