For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.

(2S,5S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2,5-DI-(METHOXYMETHYL)-PYRROLIDINE

Compound with spectra: 1 NMR

(2S,5S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2,5-DI-(METHOXYMETHYL)-PYRROLIDINE
SpectraBase Compound ID 49ovMTKKZPz
InChI InChI=1S/C31H47NO3Si/c1-26(23-32-27(24-33-5)20-21-28(32)25-34-6)15-13-14-22-35-36(31(2,3)4,29-16-9-7-10-17-29)30-18-11-8-12-19-30/h7-12,15-19,27-28H,13-14,20-25H2,1-6H3/b26-15+/t27-,28-/m0/s1
InChIKey CDIIIQYJUPXRHN-MQKFGKPMSA-N
Mol Weight 509.8 g/mol
Molecular Formula C31H47NO3Si
Exact Mass 509.332521 g/mol
Enantiomer InChIKey CDIIIQYJUPXRHN-TWNMRXRKSA-N

View Spectrum of (2S,5S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2,5-DI-(METHOXYMETHYL)-PYRROLIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1-[(4'-Methoxyphenyl)methoxy]-5-hydroxy-11-[(t-butyl)diphenylsilanyloxy]-2,2-dimethylundecan-4-one
Methyl (2S*,1'R*)-6-(tert-Butyldiphenylsilyloxy)-2-(1'-methanesulfonyloxyethyl)hexanoate
4-[4-(tert-Butyldiphenylsilyloxy)butyl]-2,2-dimethyl-4-methoxymethyl-1,3-dioxolane
6-Allyl-1-[3'-(tert-butyldiphenylsilyl)propyl]-1,2,3,6-tetradeoxy-4-O-methyl-.alpha.,D-erythro-hexopyranose
4-[(2R,3S,6R)-6-[3-[tert-butyl(diphenyl)silyl]oxypropyl]-3-methoxy-2-oxanyl]-1-butanol
3-{5'-(t-Butyl)diphenylsilyloxy]-2',2'-dimethyl-1'-methylidenepentyl}-cyclopentanone
3-{4'-[(t-Butyl)diphenylsilyloxy]-2,2-dimethyl-1-methylidenebutyl}cyclopentanone
N-(S-TRITYL-2-MERCAPTOACETYL)-O-TERT.-BUTYLDIPHENYLSILYL-3-AMINOPROPANOL
(2S-cis)-5,6-dihydro-N,N-dimethyl-2-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]-2H-pyran-5-acetamide
[1R-(1.beta.,2.beta.,3.beta.,5.beta.)]-2-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]-6-oxabicyclo[3.1.0]hexan-3-ol
Title Journal or Book Year
Zwitterionic Aza‐Claisen Rearrangements Controlled by Pyrrolidine Auxiliaries – Useful Key Steps in Convergent Enantioselective Syntheses European Journal of Organic Chemistry 2012
Other Resources
Unknown Identification

Search your unknown spectrum against the world's largest collection of reference spectra

KnowItAll Campus Solutions

KnowItAll offers faculty and students at your school access to all the tools you need for spectral analysis and structure drawing & publishing! Plus, access the world's largest spectral library.