✦ LIBER ✦

A stereospecific synthesis of 2,3-disubstituted tetrahydrofuran derivatives

✍ Scribed by Yuekun Zhao; Roy L. Beddoes; Peter Quayle

Book ID: 104214371
Publisher: Elsevier Science
Year: 1994
Tongue: French
Weight: 273 KB
Volume: 35
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)73146-7

No coin nor oath required. For personal study only.

✦ Synopsis

A stereospecific synthesis of 23-difrcncdonalised terrahydrojiuans via a rransmetallation-alhylation sequence of the corresponding 2-(tri-bwyktannyl)tetmhydrofiuans is o&r&d.

📜 SIMILAR VOLUMES

One-Pot Asymmetric Synthesis of 2- and 2

One-Pot Asymmetric Synthesis of 2- and 2,3-Disubstituted Tetrahydrofuran Derivatives

✍ Ramachandran, P. Veeraraghavan; Nair, Hari N. G.; Gagare, Pravin D. 📂 Article 📅 2012 🏛 American Chemical Society 🌐 English ⚖ 339 KB

Stereospecific synthesis of 2,3-disubsti

Stereospecific synthesis of 2,3-disubstituted 1,4-benzodioxans

✍ Gabriele Proietti; Stefano Corsano; Enzo Castagnino 📂 Article 📅 1981 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 126 KB

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Synthesis of 2,5-Disubstituted Tetrahydrofuran Derivatives.

✍ Ronaldo A. Pilli; Valeria B. Riatto 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 31 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: One-Pot Asymmetric

ChemInform Abstract: One-Pot Asymmetric Synthesis of 2- and 2,3-Disubstituted Tetrahydrofuran Derivatives.

✍ P. Veeraraghavan Ramachandran; Hari N. G. Nair; Pravin D. Gagare 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 34 KB

An expedient synthesis of 2,5-disubstitu

An expedient synthesis of 2,5-disubstituted-3-oxygenated tetrahydrofurans

✍ Caroline L. Nesbitt; Christopher S.P. McErlean 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 351 KB

Single enantiomer 2,5-disubstituted-3-oxygenated tetrahydrofurans are synthesized in as little as four steps from a commercially available epoxide. The key steps are homoallylic alcohol epoxidation, palladium-catalysed alkoxy-carbonylation-lactonisation and Mitsunobu inversion. The protocol is appli

A stereocontrolled synthesis of anti-2,5

A stereocontrolled synthesis of anti-2,5-disubstituted tetrahydrofurans

✍ Sung Ho Kang; Sung Bae Lee 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 291 KB

AxG2,Sdisubstitutad tetrahydrofurans, in which one of the subetituents is 3'-furany group, have been derived from trans-4(3'-furanyl)\_3-butenols 3-g by using iodine in diethyl ether in the presence of potassium carbonate at -78°C.