Domino aziridine ring opening and Buchwald-Hartwig type coupling-cyclization by palladium catalyst

Tetrahedron

Volumn 68, Issue 44, 2012, Pages 9090-9094

  Koteshwar Rao, R ^a   Karthikeyan, I ^a   Sekar, Govindasamy ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY MADRAS   (India)

Author keywords

Buchwald Hartwig coupling; C (aryl) N (amide) bond formation; Coupling cyclization; Cross coupling; Domino reaction

Indexed keywords

2 METHOXY 11 TOSYL 5A,6,7,8,9,10,10A,11 OCTAHYDROBENZO[B]CYCLOHEPTA[E][1,4]OXAZINE; 3 PHENYL 4 TOSYL 3,4 DIHYDRO 2H BENZO[B][1,4]OXAZINE; 3,4 DIHYDRO 2H 1,4 BENZOXAZINE; 3A,9A 7 METHOXY 9 TOSYL 1,2,3,3A,9,9A HEXAHYDROBENZO[B]CYCLOPENTA[E][1,4]OXAZINE; 4A,10A 8 PHENYL 10 TOSYL 2,3,4,4A,10,10A HEXAHYDRO 1H PHENOXAZINE; 6 CHLORO 3 PHENYL 4 TOSYL 3,4 DIHYDRO 2H BENZO[B][1,4]OXAZINE; 8 METHOXY 10 TOSYL 2,3,4,4A,10,10A HEXAHYDRO 1H PHENOXAZINE; 8 METHYL 10 TOSYL 2,3,4,4A,10,10A HEXAHYDRO 1H PHENOXAZINE; AZIRIDINE; BENZOXAZINE DERIVATIVE; BROCRESINE; CHLOROPHENOL; PALLADIUM COMPLEX; UNCLASSIFIED DRUG;

ARTICLE; BUCHWALD HARTWIG TYPE COUPLING CYCLIZATION; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; CYCLIZATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; SOLVENT EFFECT; SYNTHESIS;

EID: 84866364612     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.08.054     Document Type: Article

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