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pro vyhledávání: '"Patteti, Venukumar"'
Publikováno v:
Chemical Communications. 51:5394-5397
We reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-β-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxyt
Publikováno v:
European Journal of Organic Chemistry. 2014:8085-8093
The stereoselective synthesis of deoxy C-glycoside derivatives that have a methylene or methyl group at C-2 position was investigated by employing the Claisen rearrangement of 2-vinyloxy methyldeoxy-glycals as the synthetic precursors. The method pro
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Publikováno v:
Chem. Commun.. 50:2218-2221
Ring opening of 3-oxo-1,2-cyclopropanated sugars with thiols leads to the serendipitous discovery of the synthesis of sugar based homologated acyclic dithioacetals. These acyclic dithioacetals were found to undergo one-pot septanoside formation follo
Autor:
Perali Ramu Sridhar, Patteti Venukumar
Publikováno v:
Organic Letters. 14:5558-5561
A one-pot ring-expansion-glycosylation reaction was performed using 1,2-cyclopropanated sugars as glycosyl donors and carbohydrate O-nucleophiles as acceptors to provide septanohexose mimics of pyranose and furanose derivatives. The methodology was s
Publikováno v:
ChemInform. 45
Ring opening of 3-oxo-1,2-cyclopropanated sugars with thiols leads to the serendipitous discovery of the synthesis of sugar based homologated acyclic dithioacetals. These acyclic dithioacetals were found to undergo one-pot septanoside formation follo
Publikováno v:
European Journal of Organic Chemistry. Dec2014, Vol. 2014 Issue 36, p8085-8093. 9p.
Publikováno v:
Chemical Communications; 2015, Vol. 51 Issue 25, p5129-5151, 23p
Publikováno v:
Chemical Communications; 2015, Vol. 51 Issue 25, p5394-5397, 4p
Publikováno v:
Chemical Communications; 2014, Vol. 50 Issue 17, p2218-2221, 4p