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Regio- and Stereoselective Synthesis of Benzo-δ-sultams by Palladium-Catalyzed Hydrocarbonation of Alkynes
Abstract An efficient method for the synthesis of benzo-δ-sultams [(4 Z )-4-benzylidene-2-(arylmethyl)-3,4-dihydro-2 H -1,2-benzothiazine 1,1-dioxides] via palladium(0)-catalyzed hydrocarbonation of alkynes is presented. This method allows regioselective access to a variety of substituted benzosulta...
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Published in: | Synthesis (Stuttgart) 2016-01, Vol.48 (5), p.710-722 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
An efficient method for the synthesis of benzo-δ-sultams [(4
Z
)-4-benzylidene-2-(arylmethyl)-3,4-dihydro-2
H
-1,2-benzothiazine 1,1-dioxides] via palladium(0)-catalyzed hydrocarbonation of alkynes is presented. This method allows regioselective access to a variety of substituted benzosultams in excellent yields under mild conditions. The stereochemistry of the exocyclic double bond of the benzosultam derivatives is confirmed by single-crystal X-ray diffraction. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-0035-1561288 |