10-Alkenylphenothiazines; 2; Synthesis and mechanism of acidic hydrolysis of cis- and trans-10-2-phenylvinyl)phenothiazines; Chemistry of Heterocyclic Compounds; Vol. 22, iss. 10

Bibliographic Details
Parent link:Chemistry of Heterocyclic Compounds
Vol. 22, iss. 10.— 1986.— [P. 1152-1157]
Other Authors: Anfinogenov V. A., Napilkova O. A., Sirotkina E. E., Filimonov V. D. Viktor Dmitrievich, Khlebnikov A. I. Andrey Ivanovich
Summary:Title screen
The addition of phenothiazine to phenylacetylene in super-base media proceeds regio- and stereoselectively and leads to the predominant formation of cis-10-(2-phenylvinyl)phenothiazine, which is completely converted to its trans-isomer at 200‡C. Kinetic analysis of the acidic hydrolysis of the cis- and transisomers has allowed us to assign to it an ASE2 reaction mechanism, similar to the mechanism of hydrolysis of vinyl alkyl ethers.
Режим доступа: по договору с организацией-держателем ресурса
Language:English
Published: 1986
Subjects:
Online Access:http://dx.doi.org/10.1007/BF00473499
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=654435

MARC

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200 1 |a 10-Alkenylphenothiazines  |h 2  |i Synthesis and mechanism of acidic hydrolysis of cis- and trans-10-2-phenylvinyl)phenothiazines  |f V. A. Anfinogenov [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 14 tit.] 
330 |a The addition of phenothiazine to phenylacetylene in super-base media proceeds regio- and stereoselectively and leads to the predominant formation of cis-10-(2-phenylvinyl)phenothiazine, which is completely converted to its trans-isomer at 200‡C. Kinetic analysis of the acidic hydrolysis of the cis- and transisomers has allowed us to assign to it an ASE2 reaction mechanism, similar to the mechanism of hydrolysis of vinyl alkyl ethers. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Chemistry of Heterocyclic Compounds 
463 |t Vol. 22, iss. 10  |v [P. 1152-1157]  |d 1986 
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