Issue 12, 1999

Steroidal Aphidicolin Analogues Derived from Pregnenolone

Abstract

The conversion of pregnenolone into the 3β,5α-, 3α,5α-, 4β,5α-, 3α,4α-, 3α,4β- and 3α,4α-dihydroxy derivatives of 17β-hydroxymethyl-5α-androstane as steroidal analogues of the diterpenoid DNA polymerase α inhibitor, aphidicolin, is described.

Article information

Article type
Paper

J. Chem. Res. (S), 1999, 698-699

Steroidal Aphidicolin Analogues Derived from Pregnenolone

J. R. Hanson and K. Yildirim, J. Chem. Res. (S), 1999, 698 DOI: 10.1039/A905656D

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