Articles citing this paper
β-Acarbose. III. The Attempted Alkylation of a 1-Epivalienamine Derivative with Various Carbohydrate Triflates
Joseph C. McAuliffe and Robert V. Stick
50(3) pp.203 - 208
6 articles found in Crossref database.
Synthesis of All Eight Stereoisomeric 6‐Deoxy‐L‐hexopyranosyl Donors – Trends in Using Stereoselective Reductions or Mitsunobu Epimerizations
Frihed Tobias Gylling,
Pedersen Christian Marcus, Bols Mikael
European Journal of Organic Chemistry. 2014 2014(35). p.7924
A new synthesis of the oligosaccharide domain of acarbose
Périon Régis,
Lemée Lénaı̈ck,
Ferrières Vincent,
Duval Raphaël, Plusquellec Daniel
Carbohydrate Research. 2003 338(24). p.2779
Synthesis of carbasugar-containing non-glycosidically linked pseudodisaccharides and higher pseudooligosaccharides
Cumpstey Ian
Carbohydrate Research. 2009 344(17). p.2285
ChemInform Abstract: β‐Acarbose. Part 3. The Attempted Alkylation of a 1‐ Epivalienamine Derivative with Various Carbohydrate Triflates.
MCAULIFFE J. C., STICK R. V.
ChemInform. 1997 28(35).
Regiospecific Synthesis of 4‐Deoxy‐D‐threo‐hex‐3‐enopyranosides by Simultaneous Activation–Elimination of the Talopyranoside Axial 4‐OH with the NaH/Im2SO2 System: Manifestation of the Stereoelectronic Effect
Attolino Emanuele,
Catelani Giorgio, D’Andrea Felicia
European Journal of Organic Chemistry. 2006 2006(23). p.5279
An efficient and highly regioselective synthesis of 4-deoxy- and 2-acetamido-2,4-dideoxy-β-d-threo-hex-3-enopyranosides
Attolino Emanuele,
Catelani Giorgio, D'Andrea Felicia
Tetrahedron Letters. 2002 43(9). p.1685