✦ LIBER ✦

TMS Triflate Catalyzed Cleavage of Prenyl (3-Methylbut-2-enyl) Ester.

✍ Scribed by Mugio Nishizawa; Hirofumi Yamamoto; Ken Seo; Hiroshi Imagawa; Takumichi Sugihara

Publisher: John Wiley and Sons
Year: 2010
Weight: 34 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200241050

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Bismuth Triflate Catalyzed [1,3] Rearran

Bismuth Triflate Catalyzed [1,3] Rearrangement of Aryl 3-Methylbut-2-enyl Ethers.

✍ Thierry Ollevier; Topwe M. Mwene-Mbeja 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

A Simple, Effective and Highly Selective

A Simple, Effective and Highly Selective Cleavage of 3-Methylbut-2-enyl (Prenyl) Ethers Using p-Toluenesulfonic Acid.

✍ K. Suresh Babu; B. China Raju; P. V. Srinivas; A. Sridhar Rao; S. Praveen Kumar; 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 80 KB 👁 1 views

ChemInform Abstract: Acid-Catalyzed Rear

ChemInform Abstract: Acid-Catalyzed Rearrangements of Allyl 4-Hydroxybenzoate and 3-Methylbut-2-enyl-4-hydroxybenzoate.

✍ Sankar P. Dey; Dilip K. Dey 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 25 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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: A Facile and Select

ChemInform Abstract: A Facile and Selective Cleavage of Prenyl Esters Catalyzed by CeCl3×7H2O-NaI.

✍ J. S. Yadav; B. V. Subba Reddy; C. Venkateshwara Rao; P. K. Chand; A. R. Prasad 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 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: RuH2(CO)(PPh3)3-Cat

ChemInform Abstract: RuH2(CO)(PPh3)3-Catalyzed Arylation of Aromatic Esters Using Arylboronates via C—H Bond Cleavages.

✍ Kentaroh Kitazawa; Masashi Kotani; Takuya Kochi; Michael Langeloth; Fumitoshi Ka 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

## Abstract Ru‐catalyzed arylation of benzoic acid esters with electron‐rich arylboronates proceeds regioselectively at the ortho‐position to give sterically hindered benzoates, e.g. (III), (V) in good yields.