Microwave-assisted regiospecific synthesis of pseudohalohydrin esters

Synlett

Volumn 23, Issue 9, 2012, Pages 1384-1388

  El Khatib, Mirna ^a   Elagawany, Mohamed ^a,b,c   Todadze, Ekaterina ^a   Khelashvili, Levan ^a   El Feky, Said A ^b   Katritzky, Alan R ^a,d  

^a University of Florida ^*  (United States)

^b Zagazig University   (Egypt)

^c Misr University for Science and Technology   (Egypt)

^d KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

Author keywords

catalysis; esters; palladium; regioselectivity; ring opening

Indexed keywords

1 (1H BENZOTRIAZOL 1 YL)HEXAN 2 OL; 1 [1H BENZO[D](1,2,3)TRIAZOL 1 YL]HEXAN 2 YL 1 NAPHTHOATE; 1 [1H BENZO[D](1,2,3)TRIAZOL 1 YL]HEXAN 2 YL 2 (ADAMANTAN 1 YL)ACETATE; 1 [1H BENZO[D](1,2,3)TRIAZOL 1 YL]HEXAN 2 YL 3 PHENYLPROPANOATE; 1 [1H BENZO[D](1,2,3)TRIAZOL 1 YL]HEXAN 2 YL BENZOATE; 2 (1H BENZOTRIAZOL 1 YL) 1 PHENYLETHYL 4 ETHYLBENZOATE; 2 (1H BENZOTRIAZOL 1 YL) 1 PHENYLETHYL BENZOATE; 2 (1H BENZOTRIAZOL 1 YL) 1,2 DIPHENYLETHYL 4 ETHYLBENZOATE; 2 [1H BENZO[D](1,2,3)TRIAZOL 1 YL] 1 PHENYLETHYL 1 NAPHTHOATE; 2 [1H BENZO[D](1,2,3)TRIAZOL 1 YL] 1 PHENYLETHYL 4 NITROBENZOATE; BETA (BENZOTRIAZOL 1 YL)ETHYL ESTER; BETA (BENZOTRIAZOL 1 YL)ETHYL PSEUDOHALOHYDRIN ESTER; EPOXIDE; ESTER DERIVATIVE; N ACYLBENZOTRIAZOLE; PALLADIUM; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; MICROWAVE COOKING; REGIOSPECIFICITY; SYNTHESIS;

EID: 84860895226     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1291015     Document Type: Article

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