365236-07-3

Upstream product

• 365235-92-3 1,3,4,5-tetra-O-acetyl-2,6-anhydro-7,8-dideoxy-8-C-(trimethylsilyl)-D-glycero-L-gulo-oct-7-ynitol 
• 365235-98-9 2,6-anhydro-(R)-1,3-O-benzylidene-7,8-dideoxy-8-C-(trimethylsilyl)-D-glycero-L-gulo-oct-7-ynitol 
• 365235-95-6 2,6-anhydro-7,8-dideoxy-8-C-(trimethylsilyl)-D-glycero-L-gulo-oct-7-ynitol 
• 365236-01-7 2,6-anhydro-4,5-di-O-benzyl-(R)-1,3-O-benzylidene-7,8-dideoxy-D-glycero-L-gulo-oct-7-ynitol 

Downstream Products

• 866222-09-5 1,1'-[buta-1,3-diyne-1,4-diyl]bis[2,3,6-tri-O-benzyl-α-D-glucopyranosyl] 

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