convenient route for the synthesis of 3-substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes

S CADAMURO; I DEGANI; R FOCHI; A GATTI; Laura PISCOPO

convenient route for the synthesis of 3-substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes

S CADAMURO, I DEGANI, R FOCHI, A GATTI, Laura PISCOPO

Department of Science and Technological Innovation

Research output: Contribution to journal › Article

Abstract

3-Substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes have been obtained by hydrolysis with HgO-35% aq. HBF₄-DMSO of the intermediates 4 and 5 prepared by electrophilic substitution reactions on 2,5-bis(1,3-benzodithiol-2-yl)pyrrole. The overall yields starting from pyrrole ranged from 41-88%.

Original language	English
Journal	Journal of the Chemical Society, Perkin Transactions 1
Publication status	Published - 1996

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http://hdl.handle.net/11579/3141

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@article{eb5e09ca669747b2bc7866b852182877,

title = "convenient route for the synthesis of 3-substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes",

abstract = "3-Substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes have been obtained by hydrolysis with HgO-35% aq. HBF4-DMSO of the intermediates 4 and 5 prepared by electrophilic substitution reactions on 2,5-bis(1,3-benzodithiol-2-yl)pyrrole. The overall yields starting from pyrrole ranged from 41-88%.",

author = "S CADAMURO and I DEGANI and R FOCHI and A GATTI and Laura PISCOPO",

year = "1996",

language = "English",

journal = "Journal of the Chemical Society, Perkin Transactions 1",

issn = "0300-922X",

publisher = "Chemical Society",

}

TY - JOUR

T1 - convenient route for the synthesis of 3-substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes

AU - CADAMURO, S

AU - DEGANI, I

AU - FOCHI, R

AU - GATTI, A

AU - PISCOPO, Laura

PY - 1996

Y1 - 1996

N2 - 3-Substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes have been obtained by hydrolysis with HgO-35% aq. HBF4-DMSO of the intermediates 4 and 5 prepared by electrophilic substitution reactions on 2,5-bis(1,3-benzodithiol-2-yl)pyrrole. The overall yields starting from pyrrole ranged from 41-88%.

AB - 3-Substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes have been obtained by hydrolysis with HgO-35% aq. HBF4-DMSO of the intermediates 4 and 5 prepared by electrophilic substitution reactions on 2,5-bis(1,3-benzodithiol-2-yl)pyrrole. The overall yields starting from pyrrole ranged from 41-88%.

UR - https://iris.uniupo.it/handle/11579/3141

M3 - Article

SN - 0300-922X

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

ER -

convenient route for the synthesis of 3-substituted and 3,4-disubstituted pyrrole-2,5-dicarbaldehydes

Abstract

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