Title of article :
Synthesis of 3′-allylindoline spirobenzopyrans derived from 3-allyl-3H-indoles
Author/Authors :
Kagawa، نويسنده , , Natsuko and Takabatake، نويسنده , , Hiroki and Masuda، نويسنده , , Yoshitake، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2014
Pages :
5
From page :
6427
To page :
6431
Abstract :
In this study, 8 new spirobenzopyrans were synthesized. A novel, three-step, facile route for the synthesis of 3′-allylindoline spirobenzopyrans via 3-allyl-3H-indoles was developed. The newly synthesized spirobenzopyrans were evaluated for their photochromic properties. The presence of an allyl moiety at the 3′ position did not disturb the photochromic response. The steric effects of the diallyl groups at the 3′ position affected the interconversion between colored and colorless forms. Therefore, the allyl chain in 3′-allylindoline spirobenzopyrans can be utilized to attach these compounds to a molecular matrix. Consequently, this synthetic methodology could be readily applied to the creation of new photo-switchable materials.
Keywords :
Photochromism , palladium catalyst , allylation , indole , Spiropyran
Journal title :
Tetrahedron Letters
Serial Year :
2014
Journal title :
Tetrahedron Letters
Record number :
1891228
Link To Document :
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