JOIOYCJJOPFFOM-GOSISDBHSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 2hVG7fe5PHE |
|---|---|
| InChI | InChI=1S/C21H30N2OSi/c1-18(22-15-19-11-7-5-8-12-19)21(24)23(17-25(2,3)4)16-20-13-9-6-10-14-20/h5-14,18,22H,15-17H2,1-4H3/t18-/m1/s1 |
| InChIKey | JOIOYCJJOPFFOM-GOSISDBHSA-N |
| Mol Weight | 354.57 g/mol |
| Molecular Formula | C21H30N2OSi |
| Exact Mass | 354.21274 g/mol |
| Enantiomer InChIKey | JOIOYCJJOPFFOM-SFHVURJKSA-N |
| Racemate InChIKey | JOIOYCJJOPFFOM-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-Acetylleucine n,N-dibenzylamide
1-Benzyl-3-(but-3'-en-2'-yl)pyrrolidin-2-one
5-.alpha.-Acetyl-N-benzyl-.delat.-valerolactam
N,N-dibenzyl-2-phenoxybutanamide
ETHYL-4-(N-BENZYL-2-OXOPYRROLIDIN-3-YL)-BUTANOATE
1-Benzyl-3-chloro-4-(chloromethyl)-2-pyrrolidone
(+)-(2S,4E)-2-[N-Benzyl-N-(trimethylsilyl)methyl]amino-3-methylthio-4-hexene
N-TRIFLUOROACETYL-GLYCYL-[N-BENZYL-N-[4-TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
N-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
N-TERT.-BUTYLOXYCARBONYL-BETA-ALANYL-[N-BENZYL-N-[4-TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
| Title | Journal or Book | Year |
|---|---|---|
| A Synthetic Strategy for the Preparation of Cyclic Peptide Mimetics Based on SET-Promoted Photocyclization Processes | Journal of the American Chemical Society | 2003 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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