(2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

Base Information

Chemical Name:(2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol
CAS No.:1255646-79-7
Molecular Formula:C₄₂H₆₈O₉
Molecular Weight:716.997
Hs Code.:

(2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

Synonyms:(2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

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Chemical Property of (2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

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Technology Process of (2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

There total 1 articles about (2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol 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:

: 6737-11-7
2-acetoxy-3-butene

: 1255646-78-6
2-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)ethanol

: 1255646-79-7
(2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

: (2R,3R)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

Guidance literature:: With potassium phosphate; C₅₄H₄₂IrN₂O₈P₂; In tetrahydrofuran; water; at 70 ℃; for 48h; optical yield given as %de; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/ja1082798

Reference yield: 52.0%

: 1255646-79-7
(2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol

: 107-02-8,25068-14-8
acrolein

: 1255646-80-0
(4S,5R,E)-5-hydroxy-6-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-4-methylhex-2-enal

Guidance literature:: (2R,3S)-1-((4S,6S)-6-(((4S,6S)-6-(((4R,6R)-6-((3S,4S,E)-4-(4-methoxybenzyloxy)-3,5-dimethylhex-1-enyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)methyl)-2,2-dimethyl-1,3-dioxan-4-yl)-3-methylpent-4-en-2-ol; acrolein; With Hoveyda-Grubbs catalyst second generation; In 1,2-dichloro-ethane; at 60 ℃; for 24h; Inert atmosphere;

acrolein; With Hoveyda-Grubbs catalyst second generation; In 1,2-dichloro-ethane; at 60 ℃; for 24h; stereoselective reaction; Inert atmosphere;
DOI:10.1021/ja1082798