(E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol

Base Information

Chemical Name:(E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol
CAS No.:1198465-44-9
Molecular Formula:C₂₃H₂₇NO₉
Molecular Weight:461.469
Hs Code.:

Synonyms:(E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol

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Chemical Property of (E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol

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Technology Process of (E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol

There total 3 articles about (E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol 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: 66.0%

: 1198465-29-0
(6Z)-3,6-anhydro-1,2:4,5-bis-O-(1-methylethylidene)-7-bromo-7-deoxy-7-(3-nitrophenyl)-L-gluco-hept-6-enitol

: 82101-74-4
methyl (E)-3-(tributylstannyl)acrylate

: 1198465-44-9
(E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trifuran-2-yl-phosphane; In toluene; at 140 ℃; for 0.75h; Microwave irradiation;
DOI:10.1016/j.tetlet.2009.09.019

Reference yield:

: 13331-27-6
m-nitrobenzene boronic acid

: 1198465-44-9
(E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate / 1,2-dimethoxyethane; water / 0.17 h

1.2: 24 h / 85 °C

2.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trifuran-2-yl-phosphane / toluene / 0.75 h / 140 °C / Microwave irradiation

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trifuran-2-yl-phosphane; potassium carbonate; In 1,2-dimethoxyethane; water; toluene; 1.2: Suzuki coupling / 2.1: Stille coupling;
DOI:10.1002/ejoc.201100949

Reference yield:

: (3aR,6S,6aR)-4-Dibromomethylene-6-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole

: 1198465-44-9
(E)-2,5-anhydro-1-(2-E-(methoxycarbonyl)ethenyl)-1-(3-nitrophenyl)-1-deoxy-3,4:6,7-di-O-isopropylidene-D-gulo-hept-1-enitol

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate / 1,2-dimethoxyethane; water / 0.17 h

1.2: 24 h / 85 °C

2.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trifuran-2-yl-phosphane / toluene / 0.75 h / 140 °C / Microwave irradiation

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trifuran-2-yl-phosphane; potassium carbonate; In 1,2-dimethoxyethane; water; toluene; 1.2: Suzuki coupling / 2.1: Stille coupling;
DOI:10.1002/ejoc.201100949