✦ LIBER ✦

ChemInform Abstract: Total Synthesis of (+)-Isozingiberene via a Novel and Efficient Hoffmann Elimination Reaction.

✍ Scribed by J. B. BHONSLE

Book ID: 112022463
Publisher: John Wiley and Sons
Year: 2010
Weight: 32 KB
Volume: 26
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199525204

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of Carba-D-fructofuranose via a Novel Metathesis Reaction.

✍ Mohindra Seepersaud; Yousef Al-Abed 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

ChemInform Abstract: Efficient Total Syn

ChemInform Abstract: Efficient Total Synthesis of Piceatannol via (E)-Selective Wittig—Horner Reaction.

✍ Su Young Han; Hyun Suck Lee; Da Hye Choi; Jung Woon Hwang; Deok Mo Yang; Jong-Ga 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 22 KB 👁 2 views

ChemInform Abstract: A Novel Synthesis o

ChemInform Abstract: A Novel Synthesis of Isocyanates and Ureas via β-Elimination of Haloform.

✍ S. Braverman; M. Cherkinsky; L. Kedrova; A. Reiselman 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

ChemInform Abstract: Efficient Total Syn

ChemInform Abstract: Efficient Total Synthesis of Novel Bioactive Microbial Metabolites

✍ Toshiaki Sunazuka; Tomoyasu Hirose; Satoshi Omura 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 15 KB 👁 1 views

ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of Octalactin A via Ring-Closing Metathesis Reaction.

✍ Keith R. Buszek; Nagaaki Sato; Youngmee Jeong 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 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: Total Synthesis of

ChemInform Abstract: Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology.

✍ A. X. XIANG; D. A. WATSON; T. LING; E. A. THEODORAKIS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology. -The key steps in the synthesis of the title compound (VI) are stereoselective homoallenylboration of the aldehyde (II) and regio-and stereoselective epoxidation of the resulting diene (IV). -(XIANG, A. X.;