Push–pull substitution versus intrinsic or packing related N–N gauche preferences in azines. Synthesis, crystal structures and packing of asymmetrical acetophenone azines-Reference-Cited by-同舟云学术

Push–pull substitution versus intrinsic or packing related N–N gauche preferences in azines. Synthesis, crystal structures and packing of asymmetrical acetophenone azines

Published:1995 Issue:12 Volume: Page:2311-2317
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Chen Grace Shiahuy,Wilbur Jason K.,Barnes Charles L.,Glaser Rainer

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1995/P2/P29950002311

Reference47 articles.

1. Conjugation in azines. Stereochemical analysis of benzoylformate azines in the solid state, in solution, and in the gas phase

2. Stereochemistry and Stereoelectronics of Azines. A Solid State Study of Symmetrical, (E,E)-Configured, Para-Substituted (H, F, Cl, Br, CN) Acetophenone Azines

3. Polymorphism and C?N?N?C Conformational Isomers of Azines: X-ray Crystal and Ab Initio Structures of Two Rotational Isomers of Methyl (para-Tolyl) Ketone Azine

4. Comparative analysis of crystal structures of E,E-configured para-substituted acetophenone azines with halogen, oxygen, nitrogen and carbon functional groups

5. R. Grashey , ‘Azomethine Imines’ in A. Padwa, 1,3-Dipolar Cycloaddition Chemistry, eds. D. C. Taylort and A. Weissberger;

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