✦ LIBER ✦

ChemInform Abstract: Towards Taxol Synthesis

✍ Scribed by David Crich

Publisher: John Wiley and Sons
Year: 2010
Weight: 22 KB
Volume: 31
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200011274

No coin nor oath required. For personal study only.

✦ Synopsis

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 via the “References” option.

📜 SIMILAR VOLUMES

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Intramolecular Diels-Alder Reactions Towards the Synthesis of a Taxol C-Ring Precursor.

✍ L. GRIMAUD; J.-P. FEREZOU; J. PRUNET; J.-Y. LALLEMAND 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

ChemInform Abstract: Asymmetric Total Sy

ChemInform Abstract: Asymmetric Total Synthesis of Taxol®.

✍ Teruaki Mukaiyama; et al. et al. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

ChemInform Abstract: Enantioselective To

ChemInform Abstract: Enantioselective Total Synthesis of (-)-Taxol.

✍ Hiroyuki Kusama; Ryoma Hara; Shigeru Kawahara; Toshiyuki Nishimori; Hajime Kashi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 KB 👁 3 views

ChemInform Abstract: Enantioselective To

ChemInform Abstract: Enantioselective Total Synthesis of Taxol.

✍ Koichiro Morihira; Ryoma Hara; Shigeru Kawahara; Toshiyuki Nishimori; Nobuhito N 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 2 views

ChemInform Abstract: Natural Taxols

✍ Biswanath Das; A. Kashinatham; G. Anjani 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 KB

ChemInform Abstract: Practical Synthesis

ChemInform Abstract: Practical Synthesis of Taxol Side Chain.

✍ H.-J. HA; G.-S. PARK; Y.-G. AHN; G. S. LEE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

Practical Synthesis of Taxol Side Chain. -A practical large-scale synthesis of the taxol side chain is achieved via the coupling of the chiral imine (V) with ketene acetal (II) followed by sequential reactions of lactamization, demethylation, methanolysis, and N-benzoylation. -(HA, H.-