58394-28-8Relevant academic research and scientific papers
Manipulating the enone moiety of levoglucosenone: 1,3-Transposition reactions including ones leading to isolevoglucosenone
Ma, Xinghua,Liu, Xin,Yates, Patrick,Raverty, Warwick,Banwell, Martin G.,Ma, Chenxi,Willis, Anthony C.,Carr, Paul D.
, p. 5000 - 5011 (2018/06/20)
The manipulation of the enone moiety associated with the biomass-derived, homochiral and now abundant compound levoglucosenone (1) is described. While the trichloroacetimidates derived from the allylic alcohols 3 and 4 failed to engage in Overman-type rea
Synthesis of 1,6-dihydro-3-bromo-3,4-dideoxy-β-D-threo-hex-3-enopyranose
Miftakhov, M. S.,Gaisina, I. N.,Valeev, F. A.,Shitikova, O. V.
, p. 2350 - 2352 (2007/10/03)
A preparative method for chemo- and stereoselective reduction of 3-bromolevoglucosenone into 1,6-anhydro-3-bromo-3,4-dideoxy-β-D-enopyranose using Zn(BH4)2 was developed. - Key words: 3-bromolevoglucosenone, zinc borohydride, reduction.
SYNTHESES OF 3-DEOXY-3-SUBSTITUTED-D-GLUCOSE DERIVATIVES. PART I. IMPROVEMENTS IN PREPARATION OF AND NUCLEOPHILIC ADDITIONS TO 1,6:2,3-DIANHYDRO-4-O-BENZYL-Β-D-ALLOPYRANOSE
Grindley, Bruce T.,Reimer, Gerry J.,Karlovec, Jaroslav,Brown, Robert G.,Andersob, Max
, p. 1065 - 1071 (2007/10/02)
The yield of the five-step preparation of 1,6:2,3-dianhydro-4-O-benzyl-β-D-glucopyranose from 1,6-anhydro-β-D-glucopyranose has been raised to 33percent from 12percent by modifying conditions or methods for four of the steps.It has been demonstrated that
