𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective synthesis of the C13–32 spiroacetal fragment of spirangien A

✍ Scribed by Gregg, Claire; Perkins, Michael V.


Book ID
120506275
Publisher
Elsevier Science
Year
2013
Tongue
French
Weight
746 KB
Volume
69
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of an Advanced C10–C32 Spiroac
✍ Ian Paterson; Alison D. Findlay; Edward A. Anderson 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 134 KB 👁 1 views

Spirangiens A (1, Scheme 1) and B (2), [1] isolated by the research group of Höfle from the epothilone-producing myxobacterium Sorangium cellulosum (strain So ce90), are polyketide metabolites [2] that possess potent antifungal and cytotoxic activity (IC 50 0.7 ng mL À1 against L929 mouse fibroblast

Stereoselective synthesis of the C1–C13
✍ Marie-Aude Hiebel; Béatrice Pelotier; Olivier Piva 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 486 KB

The C1-C13 fragment of bistramide A was prepared from 5-hexenoic acid in 15 linear steps and in 16% overall yield. The core 2,6-trans-tetrahydropyran ring was obtained via a kinetically controlled oxa-Michael cyclization from the corresponding chiral a,b-unsaturated hydroxyester. This precursor was

A stereoselective synthesis of the C13C
✍ Mukund K Gurjar; Siddhartha Ray Chaudhuri 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 261 KB

A stereo-controlled radical C C bond formation involving a 5-chloro-5-deoxy-L-idofurano-6,3-lactone derivative and allyltri-n-butyltin/AIBN is described. Further elaboration led to the synthesis of the C13 C19 segment of sanglifehrin A.