Reactivities of 2-C- and 3-C-Nitro-α- and β-D-erythro-Hex-2-enopyranoside Derivatives towards Methanol and AM1 Studies upon Their Stereoselectivities
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/65/2/65_2_446/_pdf
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1. ChemInform Abstract: Reactivities of 2-C- and 3-C-Nitro-α- and β-D-erythro-Hex-2- enopyranoside Derivatives Towards Methanol and AM1 Studies Upon Their Stereoselectivities.;ChemInform;2010-08-22
2. Diastereoselective addition of planar N-heterocycles to vinyl sulfone-modified carbohydrates: a new route to isonucleosides;Tetrahedron;2008-11
3. A vinyl sulfone-modified carbohydrate mediated new route to aminosugars and branched-chain sugars;Carbohydrate Research;2008-08
4. Synthesis of anomerically pure vinyl sulfone-modified pent-2-enofuranosides and hex-2-enopyranosides: a group of highly reactive Michael acceptors for accessing carbohydrate based synthons;Tetrahedron;2003-09
5. Structural studies on C-2 substitution in a new set of synthetic aminodideoxy sugars: the steric bulk at C-2 influences the puckering of the pyranose ring;Carbohydrate Research;2002-09
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