3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene

Base Information

Chemical Name:3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene
CAS No.:1158817-47-0
Molecular Formula:C₂₈H₃₉BO₃Si
Molecular Weight:462.512
Hs Code.:

Synonyms:3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene

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Chemical Property of 3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene

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Technology Process of 3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene

There total 1 articles about 3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene 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:

: 915225-49-9
2-(chlorodiphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: 138490-37-6
(±)-1-cyclohexyl-2-methylprop-2-en-1-ol

: 1158817-47-0
3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1002/anie.200805406

Reference yield: 73.0%

: 1158817-47-0
3-cyclohexyl-2-methyl-3-[diphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silyloxy]-1-propene

: 1158817-58-3
(E)-3-cyclohexyl-2-methyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(diphenylsilyloxy)prop-1-ene

Guidance literature:: With bis[(E,E)-1,5-diphenyl-3-oxopenta-1,4-diene]platinum(II); tris(para-trifluoromethyl)phenyl phosphine; In toluene; at 80 ℃; for 6h; diastereoselective reaction;
DOI:10.1002/anie.200805406