Technology Process of 1,5,6-Heptanetriol, 6-methyl-3-[3-methyl-4-(phenylmethoxy)phenyl]-,
1-acetate, (3S)-
There total 16 articles about 1,5,6-Heptanetriol, 6-methyl-3-[3-methyl-4-(phenylmethoxy)phenyl]-,
1-acetate, (3S)- 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:
- Guidance literature:
-
Multi-step reaction with 16 steps
1: PLE / dimethylsulfoxide
2: BOP; Et3N
3: LiBH4 / diethyl ether; ethanol
4: CSA / benzene
5: DIBAL-H / benzene
6: BF3*OEt2
7: 99 percent / imidazole / dimethylformamide
8: MeI; NaHCO3 / acetonitrile; H2O
9: NaBH4 / ethanol
10: 86 percent / pyridine
11: 98 percent / TBAF / tetrahydrofuran
12: SO3*pyr; DMSO; Et3N / CH2Cl2
13: K2CO3; MeOH
14: 91 percent / nBuLi / tetrahydrofuran
15: 96 percent / pyridine
16: 100 percent / AD-mix-β
With
pyridine; 1H-imidazole; methanol; sodium tetrahydroborate; lithium borohydride; n-butyllithium; pyridine-SO3 complex; AD-mix-β; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; dimethyl sulfoxide; triethylamine; methyl iodide;
In
tetrahydrofuran; diethyl ether; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; benzene;
14: Wittig reaction / 16: Sharpless asymmetric dihydroxylation;
DOI:10.1016/S0040-4039(03)01094-3
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 91 percent / nBuLi / tetrahydrofuran
2: 96 percent / pyridine
3: 100 percent / AD-mix-β
With
pyridine; n-butyllithium; AD-mix-β;
In
tetrahydrofuran;
1: Wittig reaction / 3: Sharpless asymmetric dihydroxylation;
DOI:10.1016/S0040-4039(03)01094-3