𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Assignment of 1H and 13C NMR signals of eight apocampholenic derivatives

✍ Scribed by M. Findeisen; C. Prehn; L. Hennig; K. Schulze


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
139 KB
Volume
36
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


The 1H and 13C chemical shifts of four apocampholenic aldehydes and the corresponding alcohols are reported.

1998 John ( Wiley & Sons, Ltd.


πŸ“œ SIMILAR VOLUMES


1H and 13C NMR spectral assignments of s
✍ F. Chatel; R. Faure; G. Boyer; J. P. Galy πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 53 KB πŸ‘ 2 views

The 1 H and 13 C NMR resonances of 12 tetracyclic phenothiazine derivatives were completely and unequivocally assigned by the concerted application of 1 H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradient selected correlation experiments. 1 H and 13 C chemical shifts are al

1H and 13C NMR spectral assignment of ph
✍ Etsuro Yoshimura; Rinya Kobayashi; Kazuo Furihata; Hideyuki Kajiwara; Sunao Yama πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 40 KB πŸ‘ 2 views

1 H and 13 C NMR spectral data for phytochelatin, NH 3 C --Glu-Cys 2 -Gly-COO , were assigned by a combination of one-( 1 H, 13 C) and two-dimensional (DQF-COSY, CH-COSY, HMBC) NMR experiments.

1H and 13C NMR Spectral Assignment of St
✍ Marie-ThΓ©rΓ¨se Martin; FranΓ§ois Frappier; Philippe Rasoanaivo; Milijaona Randrian πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 261 KB πŸ‘ 2 views

The indole alkaloid strychnobrasiline was studied using one-and two-dimensional NMR techniques. The interpretation of these spectra led to the complete assignments of all carbon and proton chemical shifts.

1H and 13C NMR of bioactive isochromanyl
✍ M. R. L. Santos; M. G. de Carvalho; R. Braz-Filho; E. J. Barreiro πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 218 KB πŸ‘ 1 views

Careful analysis of the 1H and 13C NMR spectra of a series of isochromanylacetylarylhydrazone derivatives indicated the diastereomeric selective character in the synthetic step used to obtain the derivatives employing acidic conditions during the condensation of the corresponding acylhydrazides with