Structure elucidation of two isomeric steroids: Photolytical and thermal reaction products from norethisterone studied by two-dimensional nuclear magnetic resonance-Reference-Cited by-同舟云学术

Structure elucidation of two isomeric steroids: Photolytical and thermal reaction products from norethisterone studied by two-dimensional nuclear magnetic resonance

Published:1985-10 Issue:5 Volume:7 Page:202-207
ISSN:0167-6555
Container-title:Pharmaceutisch Weekblad Scientific Edition
language:en
Short-container-title:Pharmaceutisch Weekblad Scientific Edition

Author:

Sedee A. G. J.,Beijersbergen Van Henegouwen G. M. J.,Guijt W.,Haasnoot C. A. G.

Publisher

Springer Science and Business Media LLC

Subject

Pharmaceutical Science,Pharmacology (medical),Pharmacology

Link

http://link.springer.com/content/pdf/10.1007/BF02307577.pdf

Reference21 articles.

1. Sedee AGJ, Beijersbergen van Henegouwen GMJ, Blaauwgeers HJA. Isolation, identification and densitometric determination of norethisterone-4β,5β-epoxide after photochemical decomposition of norethisterone. Int J Pharm 1983;15:149–58.

2. Sedee AGJ, Beijersbergen van Henegouwen GMJ, De Vries H, Guijt W, Haasnoot CAG. The photochemical decomposition of the progestogenic 19-norsteroid, norethisterone, in aqueous medium. Pharm Weekbl 1985;7:194–201.

3. Ferrer V, Gomez J, Bonet J-J. Photochemical reactions VII. A type-A rearrangement in the photolysis of a steroidal α,β-unsaturated lactone. Helv Chim Acta 1977:60:1357–60.

4. Cornell DG, Avram E, Filipescu N. Photohydration of testosterone and 4-androstene-3,17-dione in aqueous medium. Steroids 1979;33:485–94.

5. Chapman OL, Sieja JB, Welstead Jr WJ. Stereospecific rearrangement of an excited triplet ketone. J Am Chem Soc 1966;88:161–2.

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