(2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal

Base Information

Chemical Name:(2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal
CAS No.:245039-87-6
Molecular Formula:C₃₄H₅₆O₅Si₂
Molecular Weight:600.987
Hs Code.:

Synonyms:(2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal

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Chemical Property of (2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal

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Technology Process of (2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal

There total 6 articles about (2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal 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:

: C₃₅H₅₈O₄Si₂

: 245039-87-6
(2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal

Guidance literature:: With sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; In tetrahydrofuran; water;
DOI:10.1016/S0040-4039(99)00868-0

Reference yield:

: 69739-34-0
t-butyldimethylsiyl triflate

: 245039-87-6
(2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal

Guidance literature:: Multi-step reaction with 5 steps

1: lutidine

2: O₃; Me₂S / methanol

3: (R,R)-tartrate

4: i-Pr₂NEt / CH₂Cl₂

5: OsO₄; NMO; NaIO₄ / tetrahydrofuran; H₂O

With sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; dimethylsulfide; lutidine; d-tartrate ^(2-); ozone; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; water; 1: Etherification / 2: Oxidation / 3: Addition / 4: Etherification / 5: Oxidation;
DOI:10.1016/S0040-4039(99)00868-0

Reference yield:

: 91751-27-8,91797-99-8,91798-00-4,91798-01-5,106357-24-8,106357-26-0,106357-27-1,106357-25-9
(3R,4R,5S)-6-(tert-butyldiphenylsiloxy)-4-hydroxy-3,5-dimethylhexan-1-ene

: 245039-87-6
(2R,3R,4R,5S,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-methoxymethoxy-2,4,6-trimethyl-heptanal

Guidance literature:: Multi-step reaction with 5 steps

1: lutidine

2: O₃; Me₂S / methanol

3: (R,R)-tartrate

4: i-Pr₂NEt / CH₂Cl₂

5: OsO₄; NMO; NaIO₄ / tetrahydrofuran; H₂O

With sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; dimethylsulfide; lutidine; d-tartrate ^(2-); ozone; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; water; 1: Etherification / 2: Oxidation / 3: Addition / 4: Etherification / 5: Oxidation;
DOI:10.1016/S0040-4039(99)00868-0