Issue 10, 1993
From the journal:

Journal of the Chemical Society, Chemical Communications

Efficient photochemical transformation of spiro[4.n]-2,5-diones to γ-alkylidene γ-butyrolactones: its relevance to photostability of Fredericamycin A

Bipin Pandey,   Ravinder S. Reddy  and  Pradeep Kumar  

Abstract

Irradiation of a variety of model spirodiones related to the antitumour antibiotic Fredericamycin A in various solvents at 300 nm furnishes quantitative yields of γ-alkylidene γ-butyrolactones; its relevance to the typical shape alteration, photostability and consequent biological response of Fredericamycin is discussed.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39930000870
Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 870-871

Permissions

Request permissions

Efficient photochemical transformation of spiro[4.n]-2,5-diones to γ-alkylidene γ-butyrolactones: its relevance to photostability of Fredericamycin A

B. Pandey, R. S. Reddy and P. Kumar, J. Chem. Soc., Chem. Commun., 1993, 870 DOI: 10.1039/C39930000870

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements