✦ LIBER ✦

Synthesis of Biologically Active Dicarba Analogues of the Peptide Hormone Oxytocin Using Ring-Closing Metathesis

✍ Scribed by Stymiest, Jake L.; Mitchell, Bryan F.; Wong, Susan; Vederas, John C.

Book ID: 120073779
Publisher: American Chemical Society
Year: 2003
Tongue: English
Weight: 156 KB
Volume: 5
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol027160v

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Ring-Closing Metathesis in the Synthesis

Ring-Closing Metathesis in the Synthesis of Biologically Active Peptidomimetics of Apicidin A

✍ Prashant H. Deshmukh; Carsten Schulz-Fademrecht; Panayiotis A. Procopiou; David 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 161 KB 👁 2 views

## Abstract Syntheses of novel 16‐membered macrocyclic peptidomimetics are reported, which employ iterative peptide coupling followed by high yielding ring‐closing metathesis (RCM) as the key cyclization step. The target macrocyclic compounds include examples containing a (2__S__)‐amino‐8‐oxodecano

Methods for Enhancing Ring Closing Metat

Methods for Enhancing Ring Closing Metathesis Yield in Peptides: Synthesis of a Dicarba Human Growth Hormone Fragment

✍ Bianca J. van Lierop; Amanda N. Whelan; Sofianos Andrikopoulos; Roger J. Mulder; 📂 Article 📅 2010 🏛 Springer Netherlands 🌐 English ⚖ 687 KB

Synthesis of Antitumor Phosphatidylinosi

Synthesis of Antitumor Phosphatidylinositol Analogues from Glucose by the Use of Ring-Closing Olefin Metathesis.

✍ Thomas L. Andresen; Dorthe M. Skytte; Robert Madsen 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

Synthesis of novel simplified eleuthesid

Synthesis of novel simplified eleutheside analogues with potent microtubule-stabilizing activity, using ring-closing metathesis as the key-step

✍ Raphael Beumer; Pau Bayón; Piergiuliano Bugada; Sylvie Ducki; Nicola Mongelli; F 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 134 KB

ChemInform Abstract: Synthesis and anti-

ChemInform Abstract: Synthesis and anti-HIV-1 Activity of Carbocyclic Versions of Stavudine Analogues Using a Ring-Closing Metathesis.

✍ Lian Jin Liu; Ok Hyun Ko; Joon Hee Hong 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

The synthesis of highly functionalized s

The synthesis of highly functionalized seven-membered allyl ethers using palladium-catalyzed alkoxyallylation of activated olefins and ring-closing olefin metathesis

✍ Roger L Xie; James R Hauske 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 83 KB

The investigation of palladium-catalyzed alkoxyallylation of activated olefins, followed by ring-closing metathesis to synthesize functionalized seven-membered ring allyl ethers is described. The influence of the olefin substituents on the diastereoselectivity of the alkoxyallylation has also been e