An efficient route to per-O-acetylated hexofuranoses
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference34 articles.
1. See for example: (a) K. Toshima, K. Tatsuta, Chem. Rev., 93 (1993) 1503–1531.
2. (b) R.R. Schmidt, Angew. Chem., Int. Ed. Engl., 25 (1986) 212–235.
3. Manipulation of free carbohydrates via stannylene acetals. Preparation of β-per-O-acyl derivatives of d-mannose, l-rhamnose, 6-O-trityl-d-talose, and d-lyxose
4. (a) C.S. Hudson, J.M. Johnson, J. Am. Chem. Soc., 38 (1916) 1223–1228.
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3. Tetranuclear zinc cluster: a dual purpose catalyst for per-O-acetylation and de-O-acetylation of carbohydrates;RSC Advances;2016
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