Concise total synthesis of (±)-palominol and (±)-dolabellatrienone via a dianion-accelerated oxy-cope rearrangement

ChemInform Abstract: Concise Total Synth

ChemInform Abstract: Concise Total Synthesis of (.+-.)-Palominol and (.+-.)-Dolabellatrienone via a Dianion-Accelerated Oxy-Cope Rearrangement.

✍ E. J. COREY; R. S. KANIA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Concise Total Syntheses of Palominol (I)

Concise Total Syntheses of Palominol (I), Dolabellatrienone (II), β-Araneosene (III), and Isoedunol via an Enantioselective Diels—Alder Macrobicyclization.

✍ Scott A. Snyder; E. J. Corey 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 13 KB 👁 1 views

## 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, please click on HTML or PDF.

Synthesis of Functionalized Polycyclic C

Synthesis of Functionalized Polycyclic Compounds via a Novel Aromatic Oxy-Cope Rearrangement.

✍ Syed Sulaiman Hussaini; A. R. Naresh Raj; C. A. M. A. Huq 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

## 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, please click on HTML or PDF.

ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of (.+-.)-Tremulenolide A and (.+-.)-Tremulenediol A via a Stereoselective Cyclopropanation/Cope Rearrangement Annulation Strategy.

✍ H. M. L. DAVIES; B. D. DOAN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

Preparation of functionalized hydroindol

Preparation of functionalized hydroindol-3-ols via tandem aza-Cope rearrangement-mannich cyclizations. Formal total synthesis of (+)-6a-epipretazettine and related alkaloids

✍ Larry E. Overman; Hanno Wild 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 248 KB

Key steps in this approach to umaryllidaceae alkaloids containing oxidation at the R-position of the pyrroline ring are (a) copper(H)-promoted rearrangement of aminocyclopentanol 11 to afford the 3-silylhydroindole 12, and (b) oxidation of 12 by the general procedures of Kumada and Fleming to give t