New synthesis of 4,5-dihydro-1,3-oxazoles and 4,5-dihydro-1,3-oxazines, useful intermediates to enantiomerically pure amino diols. X-Ray molecular structure of (4S,5R,4′S)-1 -(4′-lodomethyl-4′-methyl-4′,5′-dihydro-1′,3′-oxazol-2′-yl)-3,4-dimethyl-5-phenylimidazolidin-2-one and (4S,5R,4′S,1″S)-1 -[4′-(1″-iodobutyl)-4′,5′-dihydro-1′,3′-oxazol-2′-yl]-3,4-dimethyl-5-phenylimidazolidin-2-one-Reference-Cited by-同舟云学术

New synthesis of 4,5-dihydro-1,3-oxazoles and 4,5-dihydro-1,3-oxazines, useful intermediates to enantiomerically pure amino diols. X-Ray molecular structure of (4S,5R,4′S)-1 -(4′-lodomethyl-4′-methyl-4′,5′-dihydro-1′,3′-oxazol-2′-yl)-3,4-dimethyl-5-phenylimidazolidin-2-one and (4S,5R,4′S,1″S)-1 -[4′-(1″-iodobutyl)-4′,5′-dihydro-1′,3′-oxazol-2′-yl]-3,4-dimethyl-5-phenylimidazolidin-2-one

Published:1990 Issue:11 Volume: Page:3095-3101
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Bongini Alessandro,Cardillo Giuliana,Orena Mario,Sabatino Piera,Sandri Sergio,Romero Marta S.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1990/P1/P19900003095

Reference24 articles.

1. An efficient synthesis of (R)-(+)- and (S)-(-)-propranolol from resolved 5-idomethyloxazo-lidin-2-ones

2. A new synthesis of both the enantiomers of 4-amino-3-hydroxybutanoic acid (gabob) and mm2 calculations for rotamers of the intermediate oxazolidin-2-on

3. Synthesis of Aminoalcohols via Perihydro-1,3-oxazin-2-ones and Absolute Configuration Assignment through MM2 Calculations

4. Diastereoselective alkylation of 3-acylimidazolidin-2-ones: synthesis of (R)- and (S)-lavandulol

5. Enantioselective synthesis of 2-benzyloxy alcohols and 1,2-diols via alkylation of chiral glycolate imides. A convenient approach to optically active glycerol derivatives

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4. Ephedrine‐Derived Imidazolidin‐2‐ones. Broad Utility Chiral Auxiliaries in Asymmetric Synthesis;Chemische Berichte;1993-12

5. Lewis acid-promoted 1,4-addition to chiral imide derivatives in the synthesis of .beta.-amino acids;The Journal of Organic Chemistry;1993-10