1 H and  13 C NMR spectral data of bioactive cage‐like polycyclic compounds | Zendy

Salles Roberta C. | Zendy; Lacerda Valdemar | Zendy; Beatriz Adilson | Zendy; Ito Felicia M. | Zendy; dos Santos Reginaldo B. | Zendy; Greco, Sandro J. | Zendy; de Castro Eustáquio V. R. | Zendy; de Lima Dênis P. | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

1 H and 13 C NMR spectral data of bioactive cage‐like polycyclic compounds

Author(s) -

Salles Roberta C.,

Lacerda Valdemar,

Beatriz Adilson,

Ito Felicia M.,

dos Santos Reginaldo B.,

Greco, Sandro J.,

de Castro Eustáquio V. R.,

de Lima Dênis P.

Publication year - 2010

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.2588

Subject(s) - chemistry , cage , carbon 13 nmr , nuclear magnetic resonance spectroscopy , stereochemistry , combinatorics , mathematics

Bioactive cage‐like polycyclic compounds have attracted the attention of several research groups because of their unique appearance and their biological activities. Their structures were established on the basis of 1 H NMR and 13 C NMR spectroscopic data. The 1 H and 13 C signal assignments and most homonuclear hydrogen coupling constants were assigned by use of techniques such as 1D 1 H and 13 C NMR and 2D gCOSY, non‐edited gHSQC and gHMBC. The gNOESY experiments proved the endo‐stereochemistry. Copyright © 2010 John Wiley & Sons, Ltd.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research