Totally regio- and stereoselective synthesis of (E)-3-arylidene-3,4-dihydro-2H-1,4-benzoxazines under palladium catalyst

Tetrahedron Letters

Volumn 51, Issue 21, 2010, Pages 2859-2861

  Chowdhury, Chinmay ^a   Brahma, Kaushik ^a   Mukherjee, Sanjukta ^a   Sasmal, Anup Kumar ^a  

^a INDIAN INSTITUTE OF CHEMICAL BIOLOGY   (India)

Author keywords

1,4 Benzoxazine; Palladium catalyst; Regio and stereoselective; Synthesis

Indexed keywords

3 ARYLIDENE 3,4 DIHYDRO 2H 1,4 BENZOXAZINE; BENZOXAZINE DERIVATIVE; PALLADIUM; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME; ROOM TEMPERATURE; STEREOCHEMISTRY;

EID: 77951094029     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.03.081     Document Type: Article

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40. II-Ar moiety; (d) reductive elimination of palladium regenerates Pd(0) and affords the product 5 with E-stereochemistry.