Title of article :
Revisit to the sulfonation of pyrroles: is the sulfonation position correct?
Author/Authors :
Mizuno، نويسنده , , Akira and Kan، نويسنده , , Yukiko and Fukami، نويسنده , , Harukazu and Kamei، نويسنده , , Tomoe and Miyazaki، نويسنده , , Kazuo and Matsuki، نويسنده , , Shinsuke and Oyama، نويسنده , , Yoshiaki، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Pages :
5
From page :
6605
To page :
6609
Abstract :
Sulfonation of pyrrole and its 1-methyl derivatives with a sulfur trioxide–pyridine complex was found to give 3-sulfonated pyrroles, but not 2-sulfonates as described in textbooks. The replacement of 1-methyl-2-tri-n-butylstannylpyrrole with trimethylsilyl chlorosulfonate, followed by quenching with aq. NaHCO3 also generated sodium 1-methylpyrrole-3-sulfonate, not 2-sulfonate.
Keywords :
Rearrangements , Bicyclic heterocyclic compounds , pyrroles , Sulfonation
Journal title :
Tetrahedron Letters
Serial Year :
2000
Journal title :
Tetrahedron Letters
Record number :
1638572
Link To Document :
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