Increasing appendage diversity on 3,4-dihydro-3-oxo-2H-1,4-benzoxazines via Aphos-Pd(OAc)2-catalyzed Suzuki-Miyaura cross-coupling of aryl chlorides

Tetrahedron

Volumn 69, Issue 48, 2013, Pages 10488-10496

  Yu, Gongli ^a   Zheng, Yu ^a,c   Wu, Jinlong ^a   Dai, Wei Min ^a,b  

^a ZHEJIANG UNIVERSITY   (China)

^b HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Hong Kong)

^c LIAONING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE   (China)

Author keywords

1,4 Benzoxazines; 2 Aminophenols; Appendage diversity; Aryl chlorides; Microwave; Suzuki Miyaura cross coupling

Indexed keywords

1,2 DICHLOROETHANE; 2 AMINOPHENOL; ALDEHYDE; ALKYL GROUP; BENZENEBORONIC ACID; BENZOXAZINE DERIVATIVE; BORONIC ACID DERIVATIVE; BROMOACETIC ACID; PALLADIUM;

ALKYLATION; ANNULATION REACTION; ARTICLE; CATALYSIS; HEATING; MICROWAVE COOKING; MICROWAVE RADIATION; PRIORITY JOURNAL; REACTION TIME; ROOM TEMPERATURE; SUZUKI REACTION;

APHOS;

EID: 84887126832     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.09.057     Document Type: Article

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