Regio- and diastereochemical aspects of the additions of Li or Zn derivatives of methoxypropene to oxazolidines derived from phenylglycinol

Synlett

Volumn , Issue 12, 2006, Pages 1855-1858

  Alladoum, Jeanne ^a   Roland, Sylvain ^a   Vrancken, Emmanuel ^a   Kadouri Puchot, Catherine ^a   Mangeney, Pierre ^a  

^a SORBONNE UNIVERSITÉ   (France)

Author keywords

amino alcohols; Methoxypropene; Organolithium and organozinc reagents; Oxazolidine

Indexed keywords

ALCOHOL DERIVATIVE; ALLYL COMPOUND; BETA AMINO ALCOHOL; ETHER; LITHIUM DERIVATIVE; METHOXYPROPENE; OXAZOLIDINE DERIVATIVE; PHENYLGLYCINOL; PROPYLENE; UNCLASSIFIED DRUG; ZINC DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; STEREOCHEMISTRY;

EID: 33747036140     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-948167     Document Type: Article

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42. 4 and evaporated. The residue was then purified by chromatography on silica gel.
43. 2: C, 76.73; H, 7.80; N, 4.71. Found: C, 76.60; H, 7.83; N, 4.69.
44. Atomic coordinates, bond lengths and angles, and thermal parameters have been deposited at the Cambridge Crystallographic Data Centre with the deposition number CCDC 293382.
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46. 4 and evaporated. The residue was purified by chromatography on silica gel.
47. Atomic coordinates, bond lengths and angles, and thermal parameters have been deposited at the Cambridge Crystallographic Data Centre with the deposition numbers CCDC 602015 for 5b, CCDC 612649 for 5d and CCDC 612650 for 5c.
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