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Literature DB >> 15586393

Short, enantioselective total synthesis of stephacidin A.

Phil S Baran¹, Carlos A Guerrero, Narendra B Ambhaikar, Benjamin D Hafensteiner.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2005 PMID： 15586393 DOI： 10.1002/anie.200461864

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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22 in total

1. Total synthesis of the Galbulimima alkaloid (-)-GB17.

Authors: Reed T Larson; Michael D Clift; Regan J Thomson
Journal: Angew Chem Int Ed Engl Date: 2012-01-27 Impact factor: 15.336

2. The Neber route to substituted indoles.

Authors: Douglass F Taber; Weiwei Tian
Journal: J Am Chem Soc Date: 2006-02-01 Impact factor: 15.419

3. Intermolecular Diels-Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and Premalbrancheamide.

Authors: Jacob G Robins; Kyu J Kim; Alex J Chinn; John S Woo; Jonathan R Scheerer
Journal: J Org Chem Date: 2016-02-26 Impact factor: 4.354

4. Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600.

Authors: Thomas J Greshock; Alan W Grubbs; Ping Jiao; Donald T Wicklow; James B Gloer; Robert M Williams
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

Review 5. Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids.

Authors: Kenneth A Miller; Robert M Williams
Journal: Chem Soc Rev Date: 2009-09-16 Impact factor: 54.564

Short, enantioselective total synthesis of stephacidin A.

1. Total synthesis of the Galbulimima alkaloid (-)-GB17.

2. The Neber route to substituted indoles.

3. Intermolecular Diels-Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and Premalbrancheamide.

4. Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600.

Review 5. Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids.

Review 6. Natural products synthesis: enabling tools to penetrate Nature's secrets of biogenesis and biomechanism.

7. Chemoselectivity: the mother of invention in total synthesis.

8. Total Synthesis of Verruculogen and Fumitremorgin A Enabled by Ligand-Controlled C-H Borylation.

9. Oxidative Coupling of Enolates, Enol Silanes and Enamines: Methods and Natural Product Synthesis.

10. Concise, asymmetric, stereocontrolled total synthesis of stephacidins A, B and notoamide B.