(E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

Base Information

Chemical Name:(E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester
CAS No.:834916-74-4
Molecular Formula:C₄₀H₆₂O₉Si₂
Molecular Weight:743.098
Hs Code.:

(E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

Synonyms:(E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

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Chemical Property of (E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

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Technology Process of (E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

There total 4 articles about (E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester 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:

: 994-30-9
triethylsilyl chloride

: 834916-74-4
(E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran / 40 °C

2: DIPEA; n-Bu₄NBr / CH₂Cl₂ / Heating

With tetrabutylammomium bromide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1002/anie.200461802

Reference yield:

: 3006-41-5,20771-09-9,25152-90-3,97232-16-1,104022-77-7,113566-67-9,113566-68-0
4,6-O-benzylidene-D-glucose

: 834916-74-4
(E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / Heating

2: Et₃N / tetrahydrofuran / 40 °C

3: DIPEA; n-Bu₄NBr / CH₂Cl₂ / Heating

With tetrabutylammomium bromide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 1: Wittig reaction;
DOI:10.1002/anie.200461802

Reference yield:

: 95561-65-2
Triphenylphosphin-allyl-methoxycarbonyl-methylen

: 834916-74-4
(E)-(4S,5S)-2-Allyl-5-(4-methoxy-benzyloxymethoxy)-5-((2R,4S,5R)-2-phenyl-5-triethylsilanyloxy-[1,3]dioxan-4-yl)-4-triethylsilanyloxy-pent-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / Heating

2: Et₃N / tetrahydrofuran / 40 °C

3: DIPEA; n-Bu₄NBr / CH₂Cl₂ / Heating

With tetrabutylammomium bromide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 1: Wittig reaction;
DOI:10.1002/anie.200461802