Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,389,628 papers from all fields of science
Search
Sign In
Create Free Account
glycosyl compound biosynthetic process
Known as:
glycosyl compound formation
, glycosyl compound biosynthesis
, glycosyl compound synthesis
Expand
The chemical reactions and pathways resulting in the formation of glycosyl compound. [GOC:pr, GOC:TermGenie]
National Institutes of Health
Create Alert
Alert
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2009
Review
2009
Glycosyl iodides. History and recent advances.
P. Meloncelli
,
Alan D. Martin
,
T. Lowary
Carbohydrate Research
2009
Corpus ID: 206467376
Highly Cited
2006
Highly Cited
2006
Sonochemistry: a powerful way of enhancing the efficiency of carbohydrate synthesis.
S. Deng
,
U. Gangadharmath
,
C. Chang
Journal of Organic Chemistry
2006
Corpus ID: 34922213
Using sonication as a means of facilitating organic reactions in carbohydrate chemistry was explored under the conditions used…
Expand
Review
2004
Review
2004
Extracellular glycosyl hydrolases from clostridia.
W. Schwarz
,
V. Zverlov
,
H. Bahl
Advances in Applied Microbiology
2004
Corpus ID: 32222396
Highly Cited
2003
Highly Cited
2003
S-Benzoxazolyl (SBox) glycosides as novel, versatile glycosyl donors for stereoselective 1,2-cis glycosylation.
A. Demchenko
,
N. N. Malysheva
,
C. De Meo
Organic Letters
2003
Corpus ID: 27196664
[reaction: see text] Novel glycosyl donors, S-benzoxazolyl (SBox) glycosides, have been synthesized, tested toward various…
Expand
2002
2002
Synthesis of 5-fluoro N-acetylglucosamine glycosides and pyrophosphates via epoxide fluoridolysis: versatile reagents for the study of glycoconjugate biochemistry.
Matthew C T Hartman
,
J. Coward
Journal of the American Chemical Society
2002
Corpus ID: 23662361
Numerous carbohydrate-processing enzymes facilitate catalysis via stabilization of positive charges on or near the C-1, C-4, C-5…
Expand
Highly Cited
2001
Highly Cited
2001
The Thioglycoside and Glycosyl Phosphite of 5-Azido Sialic Acid: Excellent Donors for the α-Glycosylation of Primary Hydroxy Groups.
Chung-Shan Yu
,
K. Niikura
,
Chun-Cheng Lin
,
Chi‐Huey Wong
Angewandte Chemie
2001
Corpus ID: 14038639
5-Azido sialyl donors with O-acetyl protecting groups are useful α-selective glycosylation reagents, especially for primary…
Expand
Highly Cited
2001
Highly Cited
2001
Synthesis of C-aryl and C-alkyl glycosides using glycosyl phosphates.
E. R. Palmacci
,
P. Seeberger
Organic Letters
2001
Corpus ID: 147440
[reaction: see text] Mannosyl and glucosyl phosphate donors were successfully used in constructing C-aryl linkages common to many…
Expand
Highly Cited
2000
Highly Cited
2000
Synthesis of a group of diosgenyl saponins with combined use of glycosyl trichloroacetimidate and thioglycoside donors
Hai Yu
,
Biao Yu
,
Xiangyang Wu
,
Y. Hui
,
Xiuwen Han
2000
Corpus ID: 94168833
With the combined use of glycosyl trichloroacetimidates and thioglycosides, a group of natural diosgenyl saponins (1–6) are…
Expand
Highly Cited
1997
Highly Cited
1997
Diastereocontrolled Synthesis of Carbon Glycosides of N-Acetylneuraminic Acid via Glycosyl Samarium(III) Intermediates.
I. Vlahov
,
Petinka I. Vlahova
,
R. Linhardt
Journal of the American Chemical Society
1997
Corpus ID: 19687358
α-O-Glycosides of N-acetylneuraminic acid (Neu5Ac, 1, Scheme 1) are often found terminating the oligosaccharide component of cell…
Expand
Highly Cited
1994
Highly Cited
1994
Characterization and differentiation of diglycosyl flavonoids by positive ion fast atom bombardment and tandem mass spectrometry.
Q. M. Li
,
M. Claeys
Biological Mass Spectrometry
1994
Corpus ID: 9357685
This study shows that fast atom bombardment (FAB) in combination with collisional activation and tandem mass spectrometric…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE