✦ LIBER ✦

ChemInform Abstract: Novel Strategy for Oligosaccharide Synthesis Featuring Reiterative Alkynol Cycloisomerization.

✍ Scribed by F. E. MCDONALD; H. Y. H. ZHU

Publisher: John Wiley and Sons
Year: 2010
Weight: 35 KB
Volume: 29
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199833249

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Pyruvated Saccharid

ChemInform Abstract: Pyruvated Saccharides - Novel Strategies for Oligosaccharide Synthesis

✍ T. ZIEGLER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 KB

ChemInform Abstract: Reverse Orthogonal

ChemInform Abstract: Reverse Orthogonal Strategy for Oligosaccharide Synthesis.

✍ Kohki Fujikawa; N. Vijaya Ganesh; Yih Horng Tan; Keith J. Stine; Alexei V. Demch 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 39 KB

ChemInform Abstract: Trityl Ethers in Ol

ChemInform Abstract: Trityl Ethers in Oligosaccharide Synthesis: A Novel Strategy for the Convergent Assembly of Oligosaccharides.

✍ G.-J. BOONS; S. BOWERS; D. M. COE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Synthesis of Methyl

ChemInform Abstract: Synthesis of Methylated Cello-oligosaccharides: Synthesis Strategy for Blockwise Methylated Cello-oligosaccharides

✍ Hiroshi Kamitakahara; Fumiaki Nakatsubo; Dieter Klemm 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 15 KB

ChemInform Abstract: Peptide Templated G

ChemInform Abstract: Peptide Templated Glycosidic Bond Formation. A New Strategy for Oligosaccharide Synthesis.

✍ Richard J. Tennant-Eyles; Benjamin G. Davis; Antony J. Fairbanks 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: A Cycloisomerizatio

ChemInform Abstract: A Cycloisomerization/Friedel—Crafts Alkylation Strategy for the Synthesis of Pyrano[3,4-b]indoles.

✍ Matthew R. Medeiros; Scott E. Schaus; John A. Jr. Porco 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

## Abstract The two‐step procedure involves a Sonogashira coupling of dihydropyran propargyl ethers with iodoanilines or iodophenols according to A) followed by Sc(OTf)~3~‐catalyzed Friedel—Crafts alkylation.