methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside

Base Information

Chemical Name:methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside
CAS No.:1085789-46-3
Molecular Formula:C₃₃H₃₂O₆S
Molecular Weight:556.679
Hs Code.:

Synonyms:methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside

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Technology Process of methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside

There total 2 articles about methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 83.0%

: 1204695-25-9
methyl 2,3-dideoxy-3-C-(p-tolylsulfonyl)-α-D-erythro-hex-2-enopyranoside

: 76-83-5
trityl chloride

: 1085789-46-3
methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside

Guidance literature:: With pyridine; at 20 ℃; for 48h; Inert atmosphere;
DOI:10.1021/jo902046g

Reference yield: 80.0%

: 76-83-5
trityl chloride

: 116113-86-1
methyl 2,3-dideoxy-4,6-O-(phenylmethylene)-3-C-p-toluenesulfonyl-α-D-erythro-hex-2-enopyranoside

: 1085789-46-3
methyl 2,3-dideoxy-3-C-p-toluenesulfonyl-6-O-trityl-α-D-erythro-hex-2-enopyranoside

Guidance literature:: methyl 2,3-dideoxy-4,6-O-(phenylmethylene)-3-C-p-toluenesulfonyl-α-D-erythro-hex-2-enopyranoside; With acetyl chloride; In methanol; at 20 ℃; for 2.5h;

trityl chloride; With pyridine; at 20 ℃; for 48h; Further stages.;
DOI:10.1016/j.tet.2008.08.050