A divergent synthetic strategy based on the regioselective reductive ring-opening of a cyclic 1,2-p-methoxybenzylidene acetal

Synthesis

Volumn 44, Issue 8, 2012, Pages 1247-1252

  Géant, Pierre Yves ^a   Martínez, Jean ^a   Rocard, Lou ^a   Salom Roig, Xavier J ^a  

^a UNIVERSITÉ DE MONTPELLIER   (France)

Author keywords

diols; neighboring group effects; protecting groups; regioselectivity; sulfoxides

Indexed keywords

DIOLS; FULLY PROTECTED; NEIGHBORING-GROUP EFFECTS; PROTECTING GROUP; REGIO-SELECTIVE; RING OPENING; SECONDARY ALCOHOLS; SULFOXIDES; SYNTHETIC STRATEGIES;

KETONES;

REGIOSELECTIVITY;

1 BENZYL 2 [[(4 METHOXYBENZYL)OXY]METHYL] 3 METHYL AZIRIDINE; 3 (BENZYLAMINO) 1 [(4 METHOXYBENZYL)OXY]BUTAN 2 OL; 3 (DIBENZYLAMINO) 1 (4 TOLYLTHIO)BUTANE 1,2 DIYL DIACETATE; 3 (DIBENZYLAMINO) 2 [(4 METHOXYBENZYL)OXY]BUTAN 1 OL; 3 (DIBENZYLAMINO) 2 [(4 METHOXYBENZYL)OXY]BUTANOIC ACID; 3 (DIBENZYLAMINO)BUTANE 1,2 DIOL; ACETAL DERIVATIVE; AZIRIDINE DERIVATIVE; CYCLIC 1,2 PARA METHOXYBENZYLIDENE ACETAL; HYDROXYAMINO ACID; N BENZYL 1 [2 (4 METHOXYPHENYL) 1,3 DIOXOLAN 4 YL]ETHANAMINE; N,N DIBENZYL 1 [2 (4 METHOXYPHENYL) 1,3 DIOXOLAN 4 YL]ETHANAMINE; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG STRUCTURE; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION;

EID: 84859599297     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1289746     Document Type: Article

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