(2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol

Base Information

Chemical Name:(2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol
CAS No.:136764-32-4
Molecular Formula:C₃₇H₄₀O₆
Molecular Weight:580.721
Hs Code.:

Synonyms:(2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol

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Chemical Property of (2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol

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Technology Process of (2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol

There total 1 articles about (2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol 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:

: 75-11-6
diiodomethane

: 136764-26-6
trans-3'-Phenyl-2'-propenyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside

: 136764-32-4
(2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol

Guidance literature:: With diethylzinc; In toluene; Product distribution; other allylic glucopyranosides; diastereoselectivity vs. reagents ratio;
DOI:10.1021/ja00021a052

Reference yield: 95.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 136764-32-4
(2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol

: 136764-17-5,145920-53-2
3'-Phenyl-2',3'-methanopropyl 2-O-<<(trifluoromethyl)sulfonyl>oxy>-3,4,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: With pyridine; In dichloromethane; a) -20 deg C to 0 deg C, 1 h, b) 0 deg C, 2 h;
DOI:10.1021/jo00056a028

Reference yield:

: 136764-32-4
(2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((1S,2S)-2-phenyl-cyclopropylmethoxy)-tetrahydro-pyran-3-ol

: 117467-65-9
1,3,4,6-Tetra-O-benzyl-2,5-anhydro-D-mannitol

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / pyridine / CH₂Cl₂ / a) -20 deg C to 0 deg C, 1 h, b) 0 deg C, 2 h

With pyridine; In dichloromethane;
DOI:10.1021/jo00056a028