Total Synthesis of Natural Products || (+)-11,11′-Dideoxyverticillin A
✍ Scribed by Li, Jie Jack; Corey, E.J.
- Book ID
- 120275651
- Publisher
- Springer Berlin Heidelberg
- Year
- 2012
- Tongue
- German
- Weight
- 1021 KB
- Edition
- 2012
- Category
- Article
- ISBN
- 3642340652
No coin nor oath required. For personal study only.
✦ Synopsis
'Total Synthesis of Natural Products' is written and edited by some of today's leaders in organic chemistry. Eleven chapters cover a range of natural products, from steroids to alkaloids. Each chapter contains an introduction to the natural product in question, descriptions of its biological and pharmacological properties and outlines of total synthesis procedures already carried out. Particular emphasis is placed on novel methodologies developed by the respective authors and their research groups. This text is ideal for graduate and advanced undergraduate students, as well as organic chemists in academia and industry.
📜 SIMILAR VOLUMES
The first enantioselective total synthesis of (+)-11,12-epoxycembrene-C (1), a novel naturally occurring cembranoxide isolated from tropical marine soft coral, was achieved via a general approach by employing an intramolecular McMurry coupling and Sharpless asymmetric epoxidation as key steps from r
## Abstract A simple and highly efficient stereoselective total synthesis of (11__β__)‐11‐methoxycurvularin (**5**), a polyketide natural product, was achieved. The synthesis commenced with a Cu‐mediated regioselective opening of (2__S__)‐2‐methyloxirane (**6**) and comprised a __Keck__ asymmetric