𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H-NMR study and conformational aspects of some bicyclo[3.2.0]heptane derivatives

✍ Scribed by André De Bruyn; Daniel Termont; Denis De Keukeleire; Marc J. O. Anteunis


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
359 KB
Volume
87
Category
Article
ISSN
0037-9646

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


1H and 13C NMR study of some polychlorob
✍ D. Botta; E. Mantica; L. Castellani; G. Dotelli; L. Zetta 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 110 KB 👁 1 views

Because of the upsurge of interest in polychlorobuta-1,3-diene derivatives as uncommon contaminants in underground water, seven congeners, the three pentachloro-and four tetrachloro-[(Z)-and (E)-1,1,3,4tetrachloro-, 1,1,4,4-tetrachloro-and (Z,Z)-1,2,3,4-tetrachloro]buta-1,3-dienes, were synthesized

1H and 13C NMR assignments and conformat
✍ Manuel Arnó; M. Luisa Marín; Ramón J. Zaragozá 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB 👁 2 views

This paper reports on the assignment of the 1H and 13C NMR spectra of 14 bicyclo[4.2.0]octane derivatives. Resonance assignments were made on the basis of one-and two-dimensional NMR techniques which included 1H, 13C, DEPT, HMQC and 1HÈ1H COSY and also 1D NOE di †erence spectroscopy. The ratio of th

Configurational 1H NMR study of opticall
✍ Cirilo García-Martínez; Yoichi Taguchi; Akihiro Oishi; Kikuko Hayamizu 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB

Four novel stereoisomers of 7-(1-phenylethyl)-2-oxa-7-azabicyclo[3.2.0]heptan-6-one were prepared under high pressure from [2 ] 2] cycloaddition of the pure enantiomers of 1-phenylethyl isocyanate and 2,3dihydrofuran. Their conformational preferences in solution and the absolute conÐgurations of the