(4S)-ETHYL-(E)-4-(2-CHLORO-2-PHENYLETHANAMIDO)-5-(TERT.-BUTYLDIPHENYLSILYLOXY)-PENT-2-ENOATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | KJrie5IQCOe |
|---|---|
| InChI | InChI=1S/C31H36ClNO4Si/c1-5-36-28(34)22-21-25(33-30(35)29(32)24-15-9-6-10-16-24)23-37-38(31(2,3)4,26-17-11-7-12-18-26)27-19-13-8-14-20-27/h6-22,25,29H,5,23H2,1-4H3,(H,33,35)/b22-21+ |
| InChIKey | AVGXHJWMVUNTCI-QURGRASLSA-N |
| Mol Weight | 550.2 g/mol |
| Molecular Formula | C31H36ClNO4Si |
| Exact Mass | 549.210213 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2E,4S)-4-[BENZYL-[(2E)-4-CHLORO-3-METHYL-2-BUTENYL]-AMINO]-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-2-PENTEN-1-OL
(5RS)-1-[(1R)-1-(TERT.-BUTYLDIPHENYLSILYLOXYMETHYL)-ALLYL]-5-HYDROXYPYRROLIDIN-2-ONE;ISOMER-A
(S)-5-(TERT.-BUTYLDIPHENYLSILOXYMETHYL)-1-(PHENYLMETHYL)-2-PYRROLIDINONE
(5S)-[(tert-Butyldiphenylsilyloxy)methyl]-1-(methoxycarbonyl)-2-pyrrolidinone
(2S)-2-[(tert-Butyldiphenylsilyloxy)methyl]-1-(benzyloxycarbonyl)-4-pyrroline
QJWHSHZVXRVQLD-UHFFFAOYSA-N
(S)-1-(t-Butyldiphenylsiloxy)-2-methoxy-3-(1-naphthylmethoxy)propane
(3S,4E,6S)-3-(TERT.-BUTYLDIMETHYLSILYLOXY)-7-(TERT.-BUTYL-DIPHENYLSILYLOXY)-4,6-DIMETHYLHEPT-4-EN-1-YL-PARA-METHOXY-BENZYLETHER
(S)-3-[(t-Butyldiphenylsilyl)oxy]-1,2-diphenylpropan-1-one
(R)-2-((TERT.-BUTOXYCARBONYL)-AMINO)-3-((TERT.-BUTYLDIPHENYLSILYL)-OXY)-2-METHYL-1-(PIVALOYLOXY)-PROPANE
| Title | Journal or Book | Year |
|---|---|---|
| Efficient tin hydride-mediated radical cyclisation of secondary amides leading to substituted pyrrolidinones. Part 2. Application to the synthesis of aromatic kainic acid analogues | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |
KnowItAll NMR Spectral Library
Author: Wiley
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