Addition of γ-silyloxyallyltins on ethyl glyoxylate: evaluation of the influence of the experimental conditions on the stereochemical course of the reaction

Tetrahedron

Volumn 66, Issue 8, 2010, Pages 1570-1580

  Lumbroso, Alexandre ^a   Kwiatkowski, Piotr ^b,c   Blonska, Anna ^b   Le Grognec, Erwan ^a   Beaudet, Isabelle ^a   Jurczak, Janusz ^b,c   Jarosz, Slawomir ^b   Quintard, Jean Paul ^a  

^a UNIVERSITÉ DE NANTES   (France)

^b INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

^c UNIVERSITY OF WARSAW   (Poland)

Author keywords

Allylstannation; Diastereoselective synthesis; Ethyl glyoxylate; Reaction mechanisms; Silyloxyallyltributyltins

Indexed keywords

ALUMINUM; BORON TRIFLUORIDE; CHROMIUM DERIVATIVE; ETHYL 3 (TERT BUTYLDIMETHYLSILYLOXY) 2 HYDROXYHEX 4 ENOATE; ETHYL GLYOXYLATE; GAMMA (TERT BUTYLDIMETHYLSILYLOXY)ALLYLTRIBUTYLTIN; GLYOXYLIC ACID DERIVATIVE; HALIDE; LEWIS ACID; SILANE DERIVATIVE; TIN DERIVATIVE; UNCLASSIFIED DRUG; YTTERBIUM;

ADDITION REACTION; ALLYLATION; ARTICLE; DIASTEREOISOMER; NUCLEAR OVERHAUSER EFFECT; OZONOLYSIS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; TEMPERATURE SENSITIVITY;

EID: 74949100827     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.12.037     Document Type: Article

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