Stereoselective synthesis of 6-oxabicyclo[3.2.1]octene via (3,5)-oxonium-ene reaction

Tetrahedron

Volumn 68, Issue 10, 2012, Pages 2261-2266

  Saha, Pipas ^a   Saikia, Anil K ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY GUWAHATI   (India)

Author keywords

Catalytic reaction; Indium (III) triflate; Oxabicyclic compound; Oxonium ene reaction; Stereoselective

Indexed keywords

(1R,5R,7R) 5 ISOPROPYL 2 METHYL 7 (2 NITROPHENYL) 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7R) 5 ISOPROPYL 2 METHYL 7 (4 NITROPHENYL) 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7R) 5 ISOPROPYL 2 METHYL 7 PHENYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7R) 5 ISOPROPYL 7 (4 METHOXYPHENYL) 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7R) 7 (3 BROMOPHENYL) 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7R) 7 (4 BROMOPHENYL) 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7R) 7 (4 CHLOROPHENYL) 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7R) 7 (4 FLUOROPHENYL) 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 5 ISOPROPYL 2 METHYL 7 PROPYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 5,7 DIISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 7 (4 BROMOBENZYL) 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 7 (4 CHLOROBENZYL) 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 7 BENZYL 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 7 CYCLOHEXYL 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 7 ETHYL 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 7 HEXYL 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; (1R,5R,7S) 7 ISOBUTYL 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 ENE; 6 OXABICYCLO[3.2.1]OCTENE; ALDEHYDE; EPOXIDE; ETHER DERIVATIVE; HYDRONIUM ION; INDIUM; INDIUM TRIFLATE; METHYL 4 ((1R,5R,7R) 5 ISOPROPYL 2 METHYL 6 OXABICYCLO[3.2.1]OCT 2 EN 7 YL)BENZOATE; TERPINEN 4 OL; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 84857062120     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.01.064     Document Type: Article

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