Technology Process of methyl (2R,3S,4S,6R,7R,8E,10S,11R)-11-[(3,4-dimethoxybenzyl)oxy]-7-hydroxy-3-methoxy-5-oxo-2-[(tert-butyldimethylsilyl)oxy]-4,6,8,10-tetramethyldodec-8-enoate
There total 21 articles about methyl (2R,3S,4S,6R,7R,8E,10S,11R)-11-[(3,4-dimethoxybenzyl)oxy]-7-hydroxy-3-methoxy-5-oxo-2-[(tert-butyldimethylsilyl)oxy]-4,6,8,10-tetramethyldodec-8-enoate 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:
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488099-65-6
methyl (2R,3S,4S,6R,7R,8E,10S,11R)-11-[(3,4-dimethoxybenzyl)oxy]-7-hydroxy-3-methoxy-5-oxo-2-[(tert-butyldimethylsilyl)oxy]-4,6,8,10-tetramethyldodec-8-enoate
- Guidance literature:
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methyl (2R,3S,4S)-3-methoxy-4-methyl-2-[(tert-butyldimethylsilyl)oxy]-5-oxoheptanoate;
With
titanium tetrachloride; N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at -78 ℃;
(2E,4S,5R)-5-(3,4-dimethoxybenzyloxy)-2,4-dimethyl-hex-2-enal;
In
dichloromethane;
Further stages.;
DOI:10.1021/ol0272343
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488099-65-6
methyl (2R,3S,4S,6R,7R,8E,10S,11R)-11-[(3,4-dimethoxybenzyl)oxy]-7-hydroxy-3-methoxy-5-oxo-2-[(tert-butyldimethylsilyl)oxy]-4,6,8,10-tetramethyldodec-8-enoate
- Guidance literature:
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Multi-step reaction with 14 steps
1.1: 99 percent / H2; Amberlyst 15 / (R)-Binap-Ru(II)Cl2 / methanol / 100 °C / 3102.97 Torr
2.1: LDA / tetrahydrofuran / -78 °C
2.2: HMPA
3.1: LAH / diethyl ether / 0 °C
4.1: TsOH / benzene / Heating
5.1: DIBAL-H / CH2Cl2 / -78 °C
6.1: (COCl)2; DMSO; Et3N / CH2Cl2 / -78 °C
7.1: 75 percent / BF3*OEt2 / CH2Cl2 / -78 °C
8.1: 2,6-di-tert-butyl-4-methylpyridine / CH2Cl2 / 23 °C
9.1: OsO4; NMO / tetrahydrofuran; acetone; H2O
9.2: Pb(OAc)4 / ethyl acetate
10.1: sodium chlorite / CH2Cl2 / 0 °C / pH 7
11.1: DDQ / CH2Cl2 / 0 °C / pH 7
12.1: TPAP; NMO
13.1: TiCl4; i-Pr2NEt / CH2Cl2 / -78 °C
13.2: 48 percent / CH2Cl2
With
sodium chlorite; osmium(VIII) oxide; lithium aluminium tetrahydride; N-methyl-2-indolinone; 2,6-di-tert-butyl-4-methylpyridine; Amberlyst 15; tetrapropylammonium perruthennate; oxalyl dichloride; boron trifluoride diethyl etherate; hydrogen; titanium tetrachloride; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; lithium diisopropyl amide;
RuCl2[(R)-BINAP];
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; acetone; benzene;
2.2: Frater-Seebach alkylation / 6.1: Swern oxidation;
DOI:10.1021/ol0272343
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488099-65-6
methyl (2R,3S,4S,6R,7R,8E,10S,11R)-11-[(3,4-dimethoxybenzyl)oxy]-7-hydroxy-3-methoxy-5-oxo-2-[(tert-butyldimethylsilyl)oxy]-4,6,8,10-tetramethyldodec-8-enoate
- Guidance literature:
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Multi-step reaction with 8 steps
1.1: LiAlH4 / diethyl ether
2.1: TsOH / benzene / Heating
3.1: DIBAL-H / CH2Cl2 / -78 °C
4.1: (COCl)2; DMSO; Et3N / CH2Cl2 / -78 °C
5.1: CH2Cl2 / 23 °C
6.1: DIBAL-H / CH2Cl2; hexane / -78 °C
7.1: SO3-pyridine; DMSO; Et3N / CH2Cl2
8.1: TiCl4; i-Pr2NEt / CH2Cl2 / -78 °C
8.2: 48 percent / CH2Cl2
With
lithium aluminium tetrahydride; oxalyl dichloride; pyridine-SO3 complex; titanium tetrachloride; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine;
In
diethyl ether; hexane; dichloromethane; benzene;
4.1: Swern oxidation / 7.1: Parikh-Doering oxidation;
DOI:10.1021/ol0272343