(+/-)-(1R,2R,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

Base Information

Chemical Name:(+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane
CAS No.:134031-39-3
Molecular Formula:C₃₁H₄₉NO₃Si
Molecular Weight:511.82
Hs Code.:

Synonyms:(+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

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Chemical Property of (+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

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Technology Process of (+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

There total 8 articles about (+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane 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: 56.0%

: 134031-38-2
(+/-)-(1R*,2S*,4S*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)benzoyl)>-6-oxabicyclo<3.1.0>hexane

: 19493-09-5
Methylenetriphenylphosphorane

: 134031-39-3
(+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

Guidance literature:: In tetrahydrofuran; at -78 - 23 ℃;
DOI:10.1021/ja00013a068

Reference yield:

: 930-30-3
cyclopent-2-enone

: 134031-39-3
(+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) t-BuLi, 2.) 2-thienylCuCNLi, 3.) Me₃SiCl

2: 91 percent / 4-(dimethylamino)pyridine / CH₂Cl₂ / 12 h / Ambient temperature

3: 1.) 1,1,3,3-tetramethyl-1,3-diphenyl-disilazane, n-BuLi, 3.) Pd(PPh₃)4

4: 1.) MeLi, 2.) t-BuLi

5: t-BuOOH, Triton B / tetrahydrofuran / 2 h / -23 °C

6: 56 percent / tetrahydrofuran / 3 h / Ambient temperature

With tert.-butylhydroperoxide; dmap; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; chloro-trimethyl-silane; 1,1,3,3-tetramethyl-1,3-diphenyldisilazane; methyllithium; tert.-butyl lithium; N-benzyl-trimethylammonium hydroxide; thien-2-yl(cyano)copper lithium; In tetrahydrofuran; dichloromethane;

Reference yield:

: 134031-33-7
(E)-3-<1-(hydroxymethyl)-1-propenyl>cyclopentanone

: 134031-39-3
(+/-)-(1R*,2R*,4R*)-4-<(1-((triisopropylsilyl)oxy)methyl)-1-(E)-propenyl>-1-<1-(2-(trimethylacetamido)phenyl)ethenyl>-6-oxabicyclo<3.1.0>hexane

Guidance literature:: Multi-step reaction with 5 steps

1: 91 percent / 4-(dimethylamino)pyridine / CH₂Cl₂ / 12 h / Ambient temperature

2: 1.) 1,1,3,3-tetramethyl-1,3-diphenyl-disilazane, n-BuLi, 3.) Pd(PPh₃)4

3: 1.) MeLi, 2.) t-BuLi

4: t-BuOOH, Triton B / tetrahydrofuran / 2 h / -23 °C

5: 56 percent / tetrahydrofuran / 3 h / Ambient temperature

With tert.-butylhydroperoxide; dmap; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; 1,1,3,3-tetramethyl-1,3-diphenyldisilazane; methyllithium; tert.-butyl lithium; N-benzyl-trimethylammonium hydroxide; In tetrahydrofuran; dichloromethane;