An asymmetric synthesis of isocarbacyclin (2) was achieved (97% ee), whose conversion to 8 has been already described, was isolated in 90% yield. The key step in the sequence from ketone 7 by the olefination-isomerization-coupling process with chiral sulfoximines. The vinylic sulfoximine 6 leading t
ChemInform Abstract: Asymmetric Synthesis of Isocarbacyclin Based on the Olefination—Isomerization—Coupling Process with Chiral Sulfoximines.
✍ Scribed by J. BUND; H.-J. GAIS; E. SCHMITZ; I. ERDELMEIER; G. RAABE
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 43 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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
## 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
Base and Cation Effects on the Suzuki Cross-Coupling of Bulky Arylboronic Acid with Halopyridines: Synthesis of Pyridylphenols. -Strong base and large size cation are shown to accelerate the rate and yield of Suzuki coupling of sterically bulky boronic acid with halopyridines. Best results are obtai