Compounds 2 and 5 have been synthesised and cyclised to form the cyclic 3′,5′-adenosine monophosphate (cAMP) analogues 3, 6 and 7. In a complementary exercise, cyclopentadiene has been converted into the phosphonic acid 16 in six steps. Compound 16 has been deprotected and cyclised to form the cyclic 3′,5′-adenosine monophosphate (cAMP) analogues 18 and 19.
J. M. L. Hillman and S. M. Roberts, J. Chem. Soc., Perkin Trans. 1, 1997, 3601 DOI: 10.1039/A704961G
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.
Please wait while we load your content...