N-Phenacyl heterocyclic salts such as isoquinolinium, quinolinium, and pyridinium bromide react quickly with benzoyl isothiocyanate in the present of triethylamine to produce 1,4- diionic organosulfur derivatives. Cyclization and dehydrogenation of 1,4-diionic organosulfurs gave thiazoloisoquinolinium, quinolinium, or pyridinium benzimidates

Efficient Synthesis of New Stable 1,4-diionic Organosulfurs and Corresponding Mesoionic Compounds fromN-Heterocyclic Ylides / Fahimeh, Shahrekipour; Reza, Heydari; Batool, Tahamipour; Hamideh, Saravani; Graiff, Claudia. - In: PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS. - ISSN 1042-6507. - 189:(2014), pp. 263-273. [10.1080/10426507.2013.819866]

Efficient Synthesis of New Stable 1,4-diionic Organosulfurs and Corresponding Mesoionic Compounds fromN-Heterocyclic Ylides

GRAIFF, Claudia
2014-01-01

Abstract

N-Phenacyl heterocyclic salts such as isoquinolinium, quinolinium, and pyridinium bromide react quickly with benzoyl isothiocyanate in the present of triethylamine to produce 1,4- diionic organosulfur derivatives. Cyclization and dehydrogenation of 1,4-diionic organosulfurs gave thiazoloisoquinolinium, quinolinium, or pyridinium benzimidates
2014
Efficient Synthesis of New Stable 1,4-diionic Organosulfurs and Corresponding Mesoionic Compounds fromN-Heterocyclic Ylides / Fahimeh, Shahrekipour; Reza, Heydari; Batool, Tahamipour; Hamideh, Saravani; Graiff, Claudia. - In: PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS. - ISSN 1042-6507. - 189:(2014), pp. 263-273. [10.1080/10426507.2013.819866]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2674474
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