Issue 11, 2009

Biogenetically inspired syntheses of alkaloid natural products

Abstract

Since the synthesis of tropinone in the early 20th century, generations of chemists have looked to nature for inspiration in developing elegant syntheses of natural products. Analyzing molecules in their native context greatly enriches the chemist’s understanding of nature’s solution to the rapid generation of molecular complexity. In this tutorial review, we examine select examples from the alkaloid literature to highlight ways in which the close interplay of chemistry and biology have resulted in the development of elaborate biosynthetic hypotheses as well as strikingly beautiful syntheses. In addition, we present a case study on this topic through the lens of our total synthesis of (+)-11,11′-dideoxyverticillin A.

Graphical abstract: Biogenetically inspired syntheses of alkaloid natural products

Article information

Article type
Tutorial Review
Submitted
18 Jun 2009
First published
23 Sep 2009

Chem. Soc. Rev., 2009,38, 3035-3050

Biogenetically inspired syntheses of alkaloid natural products

J. Kim and M. Movassaghi, Chem. Soc. Rev., 2009, 38, 3035 DOI: 10.1039/B819925F

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.

Social activity

Spotlight

Advertisements