Effect of aryl substituents on the rate of dark decolorization of photochromic spirochromenes of the indoline series-Reference-Cited by-同舟云学术

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Effect of aryl substituents on the rate of dark decolorization of photochromic spirochromenes of the indoline series

Published:1977-01 Issue:1 Volume:13 Page:67-69
ISSN:0009-3122
Container-title:Chemistry of Heterocyclic Compounds
language:en
Short-container-title:Chem Heterocycl Compd

Author:

Gal'bershtam M. A.,Przhiyalgovskaya N. M.,Samoilova N. P.,Braude E. V.,Lazarenko I. B.,Suvorov N. N.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry

Link

http://link.springer.com/content/pdf/10.1007/BF00479872.pdf

Reference14 articles.

1. E. V. Braude and M. A. Gal'bershtam, Khim. Geterotsikl. Soedin., No. 7, 943 (1974).

2. E. V. Braude and M. A. Gal'bershtam, Khim. Geterotsikl. Soedin., No. 2, 200 (1976).

3. M. A. Gal'bershtam, N. M. Przhiyalgovskaya, I. B. Lazarenko, V. S. Kononova, and N. N. Suvorov, Khim. Geterotsikl. Soedin., No. 4, 497 (1976).

4. M. A. Gal'bershtam and N. P. Samoilova, Khim. Geterotsikl. Soedin., No. 9, 1209 (1973).

5. M. A. Gal'bershtam and N. P. Samoilova, Khim. Geterotsikl. Soedin., No. 8, 1041 (1974).

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1. 5′-Substituted Indoline Spiropyrans: Synthesis and Applications;Colorants;2023-06-05

2. 1′,3′,3′-Trimethyl-6-nitrospiro[2 H -1-benzopyran-2,2′-indoline]: its thermal enantiomerization and the equilibration with its merocyanine †Chiral 2H-pyrans, Part 10. Part 9: Ref. 1. †;Tetrahedron: Asymmetry;1999-12

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