(2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol

Base Information

Chemical Name:(2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol
CAS No.:934165-95-4
Molecular Formula:C₂₇H₄₀O₅
Molecular Weight:444.612
Hs Code.:

Synonyms:(2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol

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Chemical Property of (2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol

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Technology Process of (2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol

There total 5 articles about (2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol 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: 85.0%

: 944416-00-6
C₂₇H₃₈O₅

: 934165-95-4
(2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane;
DOI:10.1016/j.tet.2007.01.067

Reference yield: 82.0%

: 944415-98-9
(2S,3S,6S)-7-benzyloxy-2-[(2S,4S,5S)-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-6-methyl-hept-4-yn-3-ol

: 934165-95-4
(2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol

Guidance literature:: With hydrogen; Wilkinson's catalyst; In benzene;
DOI:10.1016/j.tet.2007.01.067

Reference yield:

: 934165-89-6
((S)-2-methyl-but-3-ynyloxymethyl)-benzene

: 934165-95-4
(2S,3S,4S,5R,8S)-9-benzyloxy-3-(4-methoxy-benzyloxy)-2,4,8-trimethyl-nonane-1,5-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / zinc triflate; (-)-(1R,2S)-N-methyl-ephedrine; triethylamine / toluene / 24 h / 20 °C

2: 82 percent / hydrogen / Rh(PPh₃)3Cl / benzene

With hydrogen; zinc trifluoromethanesulfonate; triethylamine; Wilkinson's catalyst; In toluene; benzene; 1: Carreira asymmetric alkynylation;
DOI:10.1016/j.tet.2007.01.067