This article describes a new route to peptidosulfonamide. Our study shows how sulfinamides were first obtained via nucleophilic cleavage of 3,6-dihydrothiazine-1-oxide system and how the products can be subjected to oxidation with m-chloroperbenzoic acid to give sulfonamides in good yield. Copyright © Taylor & Francis Group, LLC.
Papandrea, G., Ponticelli, F. (2008). New Mild and Efficient Synthesis of Peptidosulfonamides. SYNTHETIC COMMUNICATIONS, 38(6), 858-865 [10.1080/00397910701845340].
New Mild and Efficient Synthesis of Peptidosulfonamides
PONTICELLI F.
2008-01-01
Abstract
This article describes a new route to peptidosulfonamide. Our study shows how sulfinamides were first obtained via nucleophilic cleavage of 3,6-dihydrothiazine-1-oxide system and how the products can be subjected to oxidation with m-chloroperbenzoic acid to give sulfonamides in good yield. Copyright © Taylor & Francis Group, LLC.
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https://hdl.handle.net/11365/6856
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