3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

Base Information

Chemical Name:3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside
CAS No.:1208260-51-8
Molecular Formula:C₃₀H₂₉NO₅S
Molecular Weight:515.63
Hs Code.:

Synonyms:3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

Suppliers and Price of 3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

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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 3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

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Technology Process of 3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

There total 1 articles about 3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside 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:

: C₃₂H₃₁NO₆S

: 1208260-52-9
3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-β-L-erythro-hexopyranoside

: 1208260-51-8
3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

Guidance literature:: With potassium carbonate; In methanol; at 20 ℃; optical yield given as %de; Inert atmosphere;
DOI:10.1016/j.carres.2009.10.010

Reference yield: 73.0%

: 1208260-51-8
3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

: 1208260-36-9
3-(1-tosyl-2-phenylindol-3-yl)prop-2-ynyl 4-azido-2,3,4,6-tetradeoxy-α-L-threo-hexopyranoside

Guidance literature:: With di-isopropyl azodicarboxylate; diphenyl phosphoryl azide; triphenylphosphine; In tetrahydrofuran; at -20 - 20 ℃; Inert atmosphere;
DOI:10.1016/j.carres.2009.10.010