(+)-(5S)-METHYL-5-(TERT.-BUTYLDIMETHYLSILANYLOXY)-2-OXO-PIPERIDINE-1-CARBOXYLATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Ljo0xYU3E2u |
|---|---|
| InChI | InChI=1S/C13H25NO4Si/c1-13(2,3)19(5,6)18-10-7-8-11(15)14(9-10)12(16)17-4/h10H,7-9H2,1-6H3/t10-/m0/s1 |
| InChIKey | XMDUPNQNYAHSLO-JTQLQIEISA-N |
| Mol Weight | 287.43 g/mol |
| Molecular Formula | C13H25NO4Si |
| Exact Mass | 287.155285 g/mol |
| Enantiomer InChIKey | XMDUPNQNYAHSLO-SNVBAGLBSA-N |
| Racemate InChIKey | XMDUPNQNYAHSLO-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-[2-(3,4-Dimethoxyphenyl)ethyl] (4S)-4-(t-butyldimethylsilyloxy)-5-(hydroxy)pentanamide
3-[6-(tert-Butyldimethylsiloxy)hexanoyl]-(S)-4-isopropyloxazolidin-2-one
(S)-5-(TERT.-BUTYLDIMETHYLSILOXYMETHYL)-1-(PHENYLMETHYL)-2-PYRROLIDINONE
tert-Butyl(dimethyl)silyl 4-([tert-butyl(dimethyl)silyl]oxy)-2-pyrrolidinecarboxylate
(2R,4S)-1-(t-Butyloxycarbonyl)-4-{[(tert-Butyl-dimethyl)silyloxy]methyl}azetidine-2-methanol
(1S,4R,5R)-5-ACYLAMINO-4-TERT.-BUTYLDIMETHYLSILYLOXY-2-CYCLOPENTEN-1-OL
(1S,4S,5R)-5-ACYLAMINO-4-TERT.-BUTYLDIMETHYLSILYLOXY-2-CYCLOPENTEN-1-OL
(R)-1-(TERT.-BUTYLOXYCARBONYL)-4-(4-CHLOROPHENYL)-2-PIPERIDINONE
(R,S)-4-[((tert-Butyldimethylsilyl)oxy)methyl]-1-(4-methoxybenzyl)-2-azetidinone
(+/-)-(2S,3S,4S)-3,4-DI-O-TERT.-BUTYLDIMETHYLSILYL-3,4-DIHYDROXY-2-METHYLPYRROLIDINE
| Title | Journal or Book | Year |
|---|---|---|
| Complementary and Stereodivergent Approaches to the Synthesis of 5-Hydroxy- and 4,5-Dihydroxypipecolic Acids from Enantiopure Hydroxylated Lactams | European Journal of Organic Chemistry | 2013 |