methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside

Base Information

Chemical Name:methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside
CAS No.:220460-30-0
Molecular Formula:C₂₀H₂₆O₅
Molecular Weight:346.423
Hs Code.:

Synonyms:methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside

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Chemical Property of methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside

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Technology Process of methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside

There total 1 articles about methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside 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: 74.0%

: 2622-05-1
allylmagnesium bromide

: 135700-48-0
methyl 4,6-O-benzylidene-3-deoxy-3-C-propenyl-α-D-arabino-hexopyranoside-2-ulose

: 220460-30-0
methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside

: methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-mannopyranoside

Guidance literature:: In tetrahydrofuran; for 2h;
DOI:10.1002/(SICI)1521-3773(19981217)37:23<3298::AID-ANIE3298>3.0.CO;2-O

Reference yield: 89.0%

: 220460-30-0
methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside

: 220460-32-2
methyl (R)-4,6-O-benzylidene-2,3-C-(but-2-ene-1,4-diyl)-3-deoxy-α-D-glucopyranoside

Guidance literature:: Grubbs catalyst first generation; In benzene; at 60 ℃; for 17h;
DOI:10.1002/(SICI)1521-3773(19981217)37:23<3298::AID-ANIE3298>3.0.CO;2-O

Reference yield:

: 220460-30-0
methyl (R)-4,6-O-benzylidene-2-C-propenyl-3-deoxy-3-C-propenyl-α-D-glucopyranoside

: (1R,1'R,2'S)-2'-formyl-2'-hydroxy-1-cyclohex-4'-ene-2-propenyl-1-benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / Cl₂((C₆H₁₁)3P)2RuCHPh / benzene / 17 h / 60 °C

2: 38 percent / NBS; BaCO₃ / CHCl₃ / 16 h / Heating

3: 50 percent / Zn / H₂O; propan-2-ol / 5 h / Heating

With N-Bromosuccinimide; Grubbs catalyst first generation; barium carbonate; zinc; In chloroform; water; isopropyl alcohol; benzene; 1: Cyclization / 2: Ring cleavage / 3: Elimination;
DOI:10.1021/jo991392z