An iodocyclization approach toward diastereoselective synthesis of highly functionalized tetrasubstituted tetrahydrofurans with 2,5-trans and 2,5-cis relationships from pyranoside derived acyclic oximes

Tetrahedron Asymmetry

Volumn 18, Issue 17, 2007, Pages 2069-2078

  Kumar, Vikas ^a   Gauniyal, Harsh Mohan ^a   Shaw, Arun K ^a  

^a CENTRAL DRUG RESEARCH INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

2,3 BIS(BENZYLOXY) 4 HYDROXY HEX 5 ENAL 2 BENZYL OXIME; 2,3 BIS(BENZYLOXY) 4 HYDROXY HEX 5 ENAL 2 METHYL OXIME; 2,3 BIS(BENZYLOXY) 4 HYDROXY HEX 5 ENAL OXIME; 3 BENZYLOXY 4 ACETYLOXY 5 IODOMETHYL TETRAHYDROFURAN 2 CARBALDEHYDE 2 BENZYL OXIME; 3 BENZYLOXY 4 HYDROXY 5 IODOMETHYL TETRAHYDROFURAN 2 CARBALDEHYDE 2 BENZYL OXIME; 3 BENZYLOXY 4 HYDROXY 5 IODOMETHYL TETRAHYDROFURAN 2 CARBALDEHYDE 2 METHYL OXIME; 3 BENZYLOXY 4 HYDROXY 5 IODOMETHYLTETRAHYDROFURAN 2 CARBALDEHYDE 2 METHYL OXIME; 3,4 BIS(BENZYLOXY) 5 VINYL TETRAHYDROFURAN 2 OL; METHYL 2,3 DIBENZYL 4,6 BENZYLIDENE ALPHA,DEXTRO MANNOPYRANOSIDE; METHYL 2,3 DIBENZYL 6 DEOXY 6 IODO ALPHA,DEXTRO MANNOPYRANOSIDE; METHYL 4,6 2 BENZYLIDENE ALPHA DEXTRO MANNOPYRANOSIDE; OXIME; PYRANOSIDE; TETRAHYDROFURAN; UNCLASSIFIED DRUG;

ARTICLE; DIASTEREOISOMER; DRUG SYNTHESIS; PRIORITY JOURNAL; SUBSTITUTION REACTION;

EID: 34748834612     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.08.030     Document Type: Article

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