Reaction of Chlorosulphonyl Isocyanate with Ethyl 4,6-Di-O-Acetyl- 2,3-D Ideoxy-Α-D-Erythru- Hex-2-Enopyranoside: A Reinvestigation
Abstract
The Minor Products of the Reaction of Chlorosulphonyl Isocyanate with a Hex-2-Enopyranoside in Ether and in Acetonitrile Include a 3-Alkoxycarbonylamino-3-Deoxy-Allal, 2-(D-Glycero-1,2-Diacetoxyethyl)furan, Two Hex-2- Enopyranosylamines. and Two C-C Linked Disaccharide Derivatives. Reaction Mechanisms Are Discussed. © Royal Society of Chemistry.
Recommended Citation
Hall, R. H., Jordaan, A., & de Villiers, O. G. (1975). Reaction of Chlorosulphonyl Isocyanate with Ethyl 4,6-Di-O-Acetyl- 2,3-D Ideoxy-Α-D-Erythru- Hex-2-Enopyranoside: A Reinvestigation. Journal of the Chemical Society, Perkin Transactions 1(7), pp. 626-629. Royal Society of Chemistry.
The definitive version is available at https://doi.org/10.1039/P19750000626
Department(s)
Business and Information Technology
International Standard Serial Number (ISSN)
1470-4358
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2023 Royal Society of Chemistry, All rights reserved.
Publication Date
01 Jan 1975
