134237-73-3

Upstream product

• 100-39-0 benzyl bromide 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 134221-37-7 phenyl 2^I,3^I,6^I,2^II,3^II,6^II, 2^III,3^III,6^III,2^IV,3^IV,6^IV,2^V,3^V,6^V,2^VI,3^VI,4^VI,6^VI-nonadeca-O-acetyl-1^I-thio-β-maltohexaoside 
• 365236-37-9 phenyl 4,6-O-benzylidene-α-D-glucopyranosyl-[(1->4)-α-D-glucopyranosyl]4-(1->4)-1-thio-β-D-glucopyranoside 

Downstream Products

• 134241-82-0 phenyl 2^I,3^I,6^I,2^II,3^II,6^II,2^III,3^III,6^III,2^IV,3^IV,6^IV,2^V,3^V,6^V,2^VI,3^VI,6^VI-octadeca-O-benzyl-1^I-thio-β-maltohexaoside 

Relevant academic research and scientific papers

Oligosaccharide analogues of polysaccharides part 22: Synthesis of cyclodextrin analogues containing a buta-1,3-diyne-1,4-diyl or a butane-1,4-diyl unit

The peracetylated hexaamylose (maltohexaose) 18 was obtained by an improved acetolysis of cyclomaltohexaose (α-cyclodextrin, α-CD, 16), and transformed into the benzyl- and 4-chlorobenzyl-protected thioglycosides 22 and 23, respectively (Scheme 2). Sequen

Modification of Cyclodextrins by Insertion of a Heterogeneous Sugar Unit into Their Skeletons. Synthesis of 2-Amino-2-deoxy-β-cyclodextrin from α-Cyclodextrin

Acetolysis of fully acetylated α-cyclodextrin 5a resulted in restricted fission of only one of the glycosidic bond to give the acyclic maltohexaose peracetate 6a in 46percent yields.Regioselective modifications of both terminals of hexasaccharide 6a were

Insertion of a D-Glucosamine Residue into the α-Cyclodextrin Skeleton; A Model Synthesis of 'Chimera Cyclodextrins'

Efficient conversion of α-cyclodextrin peracetate 2 into icosa-O-acetylmaltohexaose 3 by acetolytic fission of one glycosidic linkage, a series of manipulations including coupling with a 2-azido-2-deoxy-D-glucopyranose derivative, recyclization and final