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ChemInform Abstract: Total Synthesis of Prostaglandin F2α via Nickel-Promoted Stereoselective Cyclization of 1,3-Diene and Aldehyde.

✍ Scribed by Y. SATO; M. TAKIMOTO; M. MORI

Publisher: John Wiley and Sons
Year: 2010
Weight: 29 KB
Volume: 28
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199749258

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ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of Prostaglandin F2α Using Nickel-Catalyzed Stereoselective Cyclization of 1,3-Diene and Tethered Aldehyde via Transmetalation of Nickelacycle with Diisobutylaluminum Acetylacetonate.

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ChemInform Abstract: Stereoselective Synthesis of Nitrogen-Containing Heterocycles via Nickel-Catalyzed Cyclization of 1,3-Diene and Aldehyde: Formal Total Synthesis of (-)-Elaeokanine C.

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ChemInform Abstract: Efficient Synthesis

ChemInform Abstract: Efficient Synthesis of Pyrrolizidine and Indolizidine Derivatives Using Nickel-Catalyzed Cyclization of 1,3-Diene and Aldehyde: Formal Total Synthesis of (-)-Elaeokanine C.

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ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of (-)-Dendrobine via α-Carbonyl Radical Cyclization.

✍ C.-K. SHA; R.-T. CHIU; C.-F. YANG; N.-T. YAO; W.-H. TSENG; F.-L. LIAO; S.-L. WAN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Total Synthesis of (-)-Dendrobine via α-Carbonyl Radical Cyclization. -The title compound (X) is the major alkaloid of an ornamental orchid which is used as a tonic in traditional Chinese herbal medicine.

ChemInform Abstract: Further Studies on

ChemInform Abstract: Further Studies on Nickel-Promoted or -Catalyzed Cyclization of 1,3-Diene and a Tethered Carbonyl Group.

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ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of Heterocyclic Zinc Reagents via a Nickel- Catalyzed Radical Cyclization.

✍ A. VAUPEL; P. KNOCHEL 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Stereoselective Synthesis of Heterocyclic Zinc Reagents via a Nickel-Catalyzed Radical Cyclization. -Starting from iodides such as (I), (VI), and (X) or bromides such as ( XIII) and (XVI) a convenient method for the preparation of substituted furans is presented. In this one-pot procedure the inter