(2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

Base Information

Chemical Name:(2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran
CAS No.:214827-32-4
Molecular Formula:C₅₃H₈₄O₉SSi₃
Molecular Weight:981.567
Hs Code.:

(2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

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Chemical Property of (2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

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Technology Process of (2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

There total 1 articles about (2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran 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:

: 1825-61-2
Trimethylmethoxysilane

: 214827-31-3
(3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran-2-ol

: (2R,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

: 214827-32-4
(2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

Guidance literature:: With 4 A molecular sieve; t-butyldimethylsiyl triflate; 2,2-dimethoxy-propane; In dichloromethane; Yield given; Yields of byproduct given;
DOI:10.1016/S0040-4039(98)01577-9

Reference yield:

: 214827-32-4
(2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

: 214827-33-5
(2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-4-[2-hydroxy-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran-3,5-diol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; Yield given;
DOI:10.1016/S0040-4039(98)01577-9

Reference yield:

: 214827-32-4
(2S,3S,5S,6R)-2-(2-Benzenesulfonyl-1,1-dimethyl-ethyl)-3,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-[2-(tert-butyl-diphenyl-silanyloxy)-eth-(E)-ylidene]-2-methoxy-6-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-tetrahydro-pyran

: 214827-40-4
(2E,4E)-Octa-2,4-dienoic acid (4S,5S,7R,7aS)-5-(2-benzenesulfonyl-1,1-dimethyl-ethyl)-5-methoxy-2-oxo-7-((4R,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-ylmethyl)-4,5,7,7a-tetrahydro-2H-furo[2,3-c]pyran-4-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: TBAF / tetrahydrofuran

2: 86 percent / TPAP, NMO, molecular sieves 4 Angstroem / CH₂Cl₂

3: 76 percent / EDCI, DMAP / CH₂Cl₂

With dmap; N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 A molecular sieve; tetrabutyl ammonium fluoride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4039(98)01577-9