DIASTEREOSPECIFICITE DE LA REACTION D'UN YLURE D'AZOMETHINE DERIVE DE LA 1-PHENYL-3-METHOXYCARBONYL-3,4-DIHYDRO-β-CARBOLINE SUR QUELQUES DIPOLAROPHILES ETHYLENIQUES-Reference-Cited by-同舟云学术

DIASTEREOSPECIFICITE DE LA REACTION D'UN YLURE D'AZOMETHINE DERIVE DE LA 1-PHENYL-3-METHOXYCARBONYL-3,4-DIHYDRO-β-CARBOLINE SUR QUELQUES DIPOLAROPHILES ETHYLENIQUES

Published:2010-09-01 Issue:4 Volume:103 Page:169-175
ISSN:0037-9646
Container-title:Bulletin des Sociétés Chimiques Belges
language:en
Short-container-title:Bull. Soc. Chim. Belges

Author:

Lakhlifi Takar,An Nguyen Dinh,Schmitt GÉRard,Laude Bernard,Mercier Marie-France

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19941030409/fullpdf

Reference31 articles.

1. 1,3-Dipolar cycloaddition reactions. LIII. Question of the 1,3-dipolar nature of .DELTA.2-oxazolin-5-ones

2. 1.3‐Dipolare Cycloadditionen, LIV. Pyrrole aun Azlactonen und Acetylencarbonestern

3. 1.3‐Dipolare Cycloadditionen, LV. Δ 1 ‐Pyrroline und 7‐Aza‐bicyclo[2.2.1]heptane aus Azlactonen und aktivierten Alkenen

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4. ChemInform Abstract: Diastereospecificity of the Reaction of an Azomethine Ylide, Derived from 1-Phenyl-3-methoxycarbonyl-3,4-dihydro-β-carboline, with Ethylenic Dipolarophiles.;ChemInform;2010-08-18