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Direct sialic acid 4-OAc substitution by nitrogen, sulfur and carbon nucleophiles with retention of stereochemistry.
Bozzola, Tiago; Nilsson, Ulf J; Ellervik, Ulf.
Affiliation
  • Bozzola T; Centre for Analysis and Synthesis, Department of Chemistry, Lund University P.O. Box 124 SE-221 00 Lund Sweden ulf.ellervik@chem.lu.se.
  • Nilsson UJ; Centre for Analysis and Synthesis, Department of Chemistry, Lund University P.O. Box 124 SE-221 00 Lund Sweden ulf.ellervik@chem.lu.se.
  • Ellervik U; Centre for Analysis and Synthesis, Department of Chemistry, Lund University P.O. Box 124 SE-221 00 Lund Sweden ulf.ellervik@chem.lu.se.
RSC Adv ; 12(19): 11992-11995, 2022 Apr 13.
Article in En | MEDLINE | ID: mdl-35481106
ABSTRACT
A direct one-step nucleophilic substitution of the 4-OAc of acetyl protected Neu5Ac is presented. Previously published methods for direct substitution of the 4-OAc are limited to cyclic secondary amines. Here we present conditions that allow for a much wider range of nitrogen nucleophiles as well as thiols and cyanide, to be used. The present investigation significantly broadens the scope of 4-aminations and allows for the introduction of a wide variety of different nucleophiles.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2022 Document type: Article