Allylic activation across an Ir-Sn heterobimetallic catalyst: Nucleophilic substitution and disproportionation of allylic alcohol

Tetrahedron

Volumn 68, Issue 19, 2012, Pages 3776-3785

  Chatterjee, Paresh Nath ^a   Roy, Sujit ^b  

^a INDIAN INSTITUTE OF TECHNOLOGY   (India)

^b INDIAN INSTITUTE OF TECHNOLOGY BHUBANESWAR   (India)

Author keywords

Allylic activation; Allylic alcohol; Bimetallic catalyst; Mechanism; Nucleophilic substitution

Indexed keywords

1 (HEPTA 1,5 DIEN 4 YL) 4 METHYLBENZENE; 1 CINNAMYL 4 METHYLNAPHTHALENE; 1 METHYL 4(3 METHYLHEXA 1,5 DIENYL)BENZENE; 1,3 [BIS 1,3 DI(4 TOLYL)ALLYL] 1H INDOLE; 1,3,5 TRIMETHOXY 2 [3 (4 METHOXYPHENYL)ALLYL]BENZENE; 1,3,5 TRIMETHOXY 2 [3 (4 NITROPHENYL)ALLYL]BENZENE; 2 [4 (4 BROMOPHENYL)BUT 3 EN 2 YL] 1,3 DIPHENYLPROPANE 1,3 DIONE; 2 [4 (4 BROMOPHENYL)BUT 3 EN 2 YL] 5 METHYLTHIOPHENE; 2 METHYL 5 (4 4 TOLYLBUT 3 EN 2 YL)THIOPHENE; 2 METHYL 5 (4 PHENYLBUT 3 EN 2 YL)THIOPHENE; 3 [1,3 BIS(4 BROMOPHENYL)ALLYL]PENTANE 2,4 DIONE; 3,1,3 DI(4 TOLYL)ALLYL 1H INDOLE; 4 HYDROXY 3 (4 PHENYLBUT 3 EN 2 YL) 2H CHROMEN 2 ONE; 4,4' (HEXA 1,5 DIENE 1,3 DIYL)BIS(BROMOBENZENE); ALCOHOL DERIVATIVE; ALKENE; ALLYLIC ALCOHOL; CHALCONE; CINNAMYL ALCOHOL; POLYCYCLIC AROMATIC HYDROCARBON; SULFONAMIDE; TIN; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; CATALYST; PRIORITY JOURNAL; SUBSTITUTION REACTION; SYNTHESIS;

EID: 84859596145     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.02.054     Document Type: Article

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