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ENDO-1-ISOBUTYL-5-METHOXY-3-METHYL-7-PHENYL-4,6-DIOXA-2-AZABICYCLO-[3.2.0]-HEPT-2-ENE-7-CARBOXYLIC-ACID-TERT.-BUTYLESTER

Compound with spectra: 1 NMR

ENDO-1-ISOBUTYL-5-METHOXY-3-METHYL-7-PHENYL-4,6-DIOXA-2-AZABICYCLO-[3.2.0]-HEPT-2-ENE-7-CARBOXYLIC-ACID-TERT.-BUTYLESTER
SpectraBase Compound ID FGskHkUohcj
InChI InChI=1S/C21H29NO5/c1-14(2)13-19-20(16-11-9-8-10-12-16,17(23)26-18(4,5)6)27-21(19,24-7)25-15(3)22-19/h8-12,14H,13H2,1-7H3/t19-,20+,21-/m0/s1
InChIKey AHZZRHKEANBLEX-HBMCJLEFSA-N
Mol Weight 375.47 g/mol
Molecular Formula C21H29NO5
Exact Mass 375.204573 g/mol
Enantiomer InChIKey AHZZRHKEANBLEX-QHAWAJNXSA-N

View Spectrum of ENDO-1-ISOBUTYL-5-METHOXY-3-METHYL-7-PHENYL-4,6-DIOXA-2-AZABICYCLO-[3.2.0]-HEPT-2-ENE-7-CARBOXYLIC-ACID-TERT.-BUTYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
EXO-1-ISOBUTYL-5-METHOXY-3-METHYL-7-PHENYL-4,6-DIOXA-2-AZABICYCLO-[3.2.0]-HEPT-2-ENE-7-CARBOXYLIC-ACID-TERT.-BUTYLESTER
Title Journal or Book Year
Photocycloaddition of 5-Methoxyoxazoles to Aldehydes and ?-Keto Esters: A Comprehensive View on Stereoselectivity, Triplet Biradical Conformations, and Synthetic Applications of Paternò–Büchi Adducts Australian Journal of Chemistry 2008
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