Tetrahedron Letters

Expeditious synthesis of fluorinated styrylbenzenes and polyaromatic hydrocarbons

AV Bedekar, AR Chaudhary, MS Sundar, M Rajappa

Index: Bedekar, Ashutosh V.; Chaudhary, Anju R.; Shyam Sundar; Rajappa, Murali Tetrahedron Letters, 2013 , vol. 54, # 5 p. 392 - 396

Full Text: HTML

Citation Number: 10

Abstract

A series of fluorinated styrylbenzene derivatives were synthesized by the Mizoroki–Heck reaction using phosphine-free catalytic conditions or by adopting the one-pot Wittig–Heck reaction sequence. The fluorinated styrylbenzenes were converted into polyaromatic hydrocarbons such as phenanthrenes,[4] helicenes, and benzo [ghi] perylene by a modified photocyclization procedure involving I2-THF condition.

Related Articles:

A Simplified Wittig Synthesis Using Solid/Liquid Transfer Processes IV-Synthesis of symmetrical and asymmetrical mono-and di-olefins from terephtalic aldehyde

[Bigot, Y. Le; Delmas, M.; Gaset, A. Synthetic Communications, 1983 , vol. 13, # 2 p. 177 - 182]

Decarboxylation of p-and o-Formylcinnamic Acids to p-Formylstyrene and 1-Indanone

[Wiley; Hobson Journal of the American Chemical Society, 1949 , vol. 71, p. 2429]

Über die Darstellung einiger p-substituierter Styrolderivate

[Braun,D.; Keppler,H.-G. Monatshefte fuer Chemie, 1963 , vol. 94, # 6 p. 1250 - 1261]

Über die Darstellung einiger p-substituierter Styrolderivate

[Braun,D.; Keppler,H.-G. Monatshefte fuer Chemie, 1963 , vol. 94, # 6 p. 1250 - 1261]

Über die Darstellung einiger p-substituierter Styrolderivate

[Braun,D.; Keppler,H.-G. Monatshefte fuer Chemie, 1963 , vol. 94, # 6 p. 1250 - 1261]

More Articles...