134221-37-7

Upstream product

• 4551-15-9 phenylthiotrimethylsilane 
• 102671-24-9 icosa-O-acetyl maltohexaose 

Downstream Products

• 134237-73-3 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-heptadeca-O-benzyl-4^VI,6^VI-O-benzylidene-1^I-thio-β-maltohexaoside 

Relevant academic research and scientific papers

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