✦ LIBER ✦

Directed aromatic functionalization in natural-product synthesis: Fredericamycin A, nothapodytine B, and topopyrones B and D

✍ Scribed by Turner, Charles Dylan; Ciufolini, Marco A

Book ID: 120433101
Publisher: Beilstein Institut
Year: 2011
Tongue: English
Weight: 642 KB
Volume: 7
Category: Article
ISSN: 1860-5397
DOI: 10.3762/bjoc.7.171

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Directed Aromatic F

ChemInform Abstract: Directed Aromatic Functionalization in Natural Product Synthesis: Fredericamycin A, Nothapodytine B, and Topopyrones B and D

✍ Charles Dylan Turner; Marco A. Ciufolini 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 18 KB

A general highly efficient access to pre

A general highly efficient access to prenylated phenolic natural products. Synthesis of colletochlorins B and D

✍ Hiroyuki Saimoto; Tamejiro Hiyama 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 242 KB

A general approach is reported for the synthesis of phenolic natural products having terpenoid side chains: (1) construction of the reouisite bromophenol ethers, (2) coupling the aromatic ring with a terpenoid chain through copper(I) ate complex, and (3) ether cleavage under neutral or basic conditi

ChemInform Abstract: Gas Phase Thermolys

ChemInform Abstract: Gas Phase Thermolysis in Natural Product Synthesis

✍ A. J. H. KLUNDER; B. ZWANENBURG 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 1 views

Chemical Predisposition in Synthesis: Ap

Chemical Predisposition in Synthesis: Application to the Preparation of the Pyrrolidine Natural Products, Plakoridines A and B.

✍ Laura L. Etchells; Madeleine Helliwell; Neil M. Kershaw; Ali Sardarian; Roger C. 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

First Desymmetrization of a Centrosymmet

First Desymmetrization of a Centrosymmetric Molecule in Natural Product Synthesis: Preparation of a Key Fragment in the Synthesis of Hemibrevetoxin B

✍ Joanne M. Holland; Mark Lewis; Adam Nelson 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 88 KB

Exploitation of molecular symmetry can greatly improve the efficiency of syntheses. The symmetry embedded in the centrosymmetric AB dioxepane fragment of hemibrevetoxin B was exploited for the first time in the preparation of an established intermediate in its total synthesis. Desymmetrization of th

First Desymmetrization of a Centrosymmet

First Desymmetrization of a Centrosymmetric Molecule in Natural Product Synthesis: Preparation of a Key Fragment in the Synthesis of Hemibrevetoxin B

✍ Joanne M. Holland; Mark Lewis; Adam Nelson 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 83 KB