Synthesis of Neoglycoconjugates by the Desulfurative Rearrangement of Allylic Disulfides
Author:
Affiliation:
1. Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo8015314
Reference72 articles.
1. Allylic Selenosulfide Rearrangement: A Method for Chemical Ligation to Cysteine and Other Thiols
2. Sigmatropic Rearrangements as Tools for Amino Acid and Peptide Modification: Application of the Allylic Sulfur Ylide Rearrangement to the Preparation of Neoglycoconjugates and Other Conjugates
3. Dechalcogenative Allylic Selenosulfide and Disulfide Rearrangements: Complementary Methods for the Formation of Allylic Sulfides in the Absence of Electrophiles. Scope, Limitations, and Application to the Functionalization of Unprotected Peptides in Aqueous Media
4. Substituent Effect on the Efficiency of Desulfurizative Rearrangement of Allylic Disulfides
5. Sweet spots in functional glycomics
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