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Concerning the structure of the reaction products from 2,3-dicarbomethoxy-2H-azirine and enamines

✍ Scribed by Gerrit L'abbé; Peter van Stappen; Suzanne Toppet; Gabriel Germain; Guy Scheefer


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
109 KB
Volume
92
Category
Article
ISSN
0037-9646

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Regioselective addition of aniline to 8H
✍ N. Fixler; M. Demeunynck; M. C. Brochier; J. Garcia; J. Lhomme 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 247 KB

A combination of NMR techniques, including 13C and 1H DEPT, HMQC and HMBC experiments, was used to assign the structure of the compound formed by addition of aniline to 8H-pyrido [ 2,3,4-mn ] acridine. From this NMR study, two structures were possible. This ambiguity was removed by regioselective in