✦ LIBER ✦

ChemInform Abstract: Synthetic Study of Pinnatoxin A: Intramolecular Alkylation Approach to the G-Ring.

✍ Scribed by Aiko Nitta; Akihiro Ishiwata; Takeshi Noda; Masahiro Hirama

Publisher: John Wiley and Sons
Year: 2010
Weight: 24 KB
Volume: 30
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199934265

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthetic Study of

ChemInform Abstract: Synthetic Study of Pinnatoxin A: Intramolecular Diels—Alder Approach to the AG-Ring.

✍ Akihiro Ishiwata; Satoshi Sakamoto; Takeshi Noda; Masahiro Hirama 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB 👁 2 views

ChemInform Abstract: Paclitaxel Syntheti

ChemInform Abstract: Paclitaxel Synthetic Studies. A Diels—Alder Approach to the A-Ring.

✍ Santiago Carballares; Donald Craig; Charlotte A. L. Lane; A. Roderick MacKenzie; 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 31 KB

## 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: Synthetic Study of

ChemInform Abstract: Synthetic Study of Pinnatoxin A: Stereoselective Synthesis of the BCD-Ring Unit, a Novel 6,5,6-Bis-spiroketal System.

✍ T. NODA; A. ISHIWATA; S. UEMURA; S. SAKAMOTO; M. HIRAMA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB

ChemInform Abstract: An Intramolecular S

ChemInform Abstract: An Intramolecular Sulfoxide Alkylation—Elimination Approach to the [1,2,3]Triazolo[1,5-a]pyrimidine Ring System.

✍ Karl R. Gibson; Steven R. Thomas; Michael Rowley 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: Synthetic Studies o

ChemInform Abstract: Synthetic Studies of Forskolin. A Diels-Alder Approach to Corey′s Endoperoxide.

✍ H.-J. LIU; X. SHANG 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

ChemInform Abstract: A New Synthetic App

ChemInform Abstract: A New Synthetic Approach to Forskolin: Construction of the ABC Ring System from D-Galactose.

✍ I. HANNA; P. WLODYKA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

The functionalized tricyclic framework (XI) of the diterpene forskolin is synthesized by an intramolecular Diels-Alder reaction of the dienyne (VII), which is obtained by stereoselective introduction of the C side chains at C-1 and C-2 of tri-O-acetyl-D-galactal (I) via C-Ferrier and Claisen-Ireland