(3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester

Base Information

Chemical Name:(3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester
CAS No.:234434-02-7
Molecular Formula:C₄₆H₅₄O₇Si
Molecular Weight:747.016
Hs Code.:

Synonyms:(3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester

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Chemical Property of (3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester

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Technology Process of (3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester

There total 8 articles about (3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic 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: 86.0%

: phenylmagnesium bromide

: 234434-00-5
(E)-(4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-5-phenyl-hept-2-enoic acid methyl ester

: 234434-02-7
(3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester

Guidance literature:: With copper(l) iodide; chloro-trimethyl-silane; at -78 ℃;
DOI:10.1016/S0040-4039(99)00783-2

Reference yield:

: phenylmagnesium bromide

: 234434-02-7
(3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 86 percent / CuI; TMSCl / tetrahydrofuran / -78 °C

2: KHMDS; (1S)-(+)-(10-camphorsulfonyl)oxaziridine / tetrahydrofuran

4: Dibal-H

7: 86 percent / CuI; TMSCl / -78 °C

With copper(l) iodide; chloro-trimethyl-silane; (+)-(10-camphorsulfonyl) oxaziridine; potassium hexamethylsilazane; diisobutylaluminium hydride; In tetrahydrofuran; 1: Addition / 2: hydroxylation / 3: Etherification / 4: Reduction / 5: Swern oxidation / 6: Wittig reaction / 7: Addition;
DOI:10.1016/S0040-4039(99)00783-2

Reference yield:

: 139190-51-5
Methyl (4S,E)-4-(benzyloxymethoxy)-5-(tert-butyldiphenylsiloxy)-2-pentenoate

: 234434-02-7
(3S,4R,5S,6S)-6-Benzyloxymethoxy-7-(tert-butyl-diphenyl-silanyloxy)-4-methoxymethoxy-3,5-diphenyl-heptanoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 86 percent / CuI; TMSCl / tetrahydrofuran / -78 °C

2: KHMDS; (1S)-(+)-(10-camphorsulfonyl)oxaziridine / tetrahydrofuran

4: Dibal-H

7: 86 percent / CuI; TMSCl / -78 °C

With copper(l) iodide; chloro-trimethyl-silane; (+)-(10-camphorsulfonyl) oxaziridine; potassium hexamethylsilazane; diisobutylaluminium hydride; In tetrahydrofuran; 1: Addition / 2: hydroxylation / 3: Etherification / 4: Reduction / 5: Swern oxidation / 6: Wittig reaction / 7: Addition;
DOI:10.1016/S0040-4039(99)00783-2