✦ LIBER ✦

Combinatorial chemistry using polymer-supported reagents

✍ Scribed by Stephen W Kaldor; Miles G Siegel

Book ID: 104414989
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 478 KB
Volume: 1
Category: Article
ISSN: 1367-5931
DOI: 10.1016/s1367-5931(97)80115-9

No coin nor oath required. For personal study only.

✦ Synopsis

During the past several years, the field of combinatorial chemistry has expanded to include not only solid- and solution-phase methods for expedited compound synthesis, but also hybrid approaches that span these two extremes. In particular, polymer-supported reagents have emerged as useful combinatorial chemistry tools for the discovery and optimization of new pharmaceutical leads.

📜 SIMILAR VOLUMES

ChemInform Abstract: Combinatorial Chemi

ChemInform Abstract: Combinatorial Chemistry Using Polymer-Supported Reagents

✍ S. W. KALDOR; M. G. SIEGEL 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 2 views

Advances in Microwave-Assisted Combinato

Advances in Microwave-Assisted Combinatorial Chemistry Without Polymer-Supported Reagents

✍ Rafael Martinez-Palou 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 11 KB 👁 1 views

Advances in Microwave-Assisted Combinato

Advances in Microwave-Assisted Combinatorial Chemistry Without Polymer-Supported Reagents

✍ Rafael Martínez-Palou 📂 Article 📅 2006 🏛 Springer 🌐 English ⚖ 544 KB

Polymer-Supported Reagents

✍ Georges Gelbard 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 49 KB

Polymer-supported Mitsunobu ether format

Polymer-supported Mitsunobu ether formation and its use in combinatorial chemistry

✍ Viktor Krchňák; Zuzka Flegelová; Aleksandra S. Weichsel; Michal Lebl 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 214 KB

Sulfenylation chemistry using polymer-su

Sulfenylation chemistry using polymer-supported sulfides

✍ David C. Forbes; Sampada V. Bettigeri; Nahla N. Al-Azzeh; Brian P. Finnigan; Jos 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 207 KB

Clean sulfenylations are observed upon reaction of activated methylenes with phenyl succinimidyl sulfide. When working with diethyl benzylmalonate, the sulfenylated product can be selectively oxidized and thermally fragmented affording phenylsulfenic acid, initially, and diethyl benzylidenemalonate.