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ChemInform Abstract: Synthesis of the Tricyclic Portions of Batzelladines A, B and D. Revision of the Stereochemistry of Batzelladines A and D.

✍ Scribed by B. B. SNIDER; J. CHEN; A. D. PATIL; A. J. FREYER

Book ID: 112042154
Publisher: John Wiley and Sons
Year: 2010
Weight: 32 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199652258

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ChemInform Abstract: Stereoselective Synthesis of Tricyclic Guanidine Systems: Confirmation of the Stereochemistry of Batzelladine F Left-Hand Tricyclic Guanidine Portion.

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Total Synthesis of (+)-Batzelladine A an

Total Synthesis of (+)-Batzelladine A and (-)-Batzelladine D, and Identification of Their Target Protein.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Total Synthesis of (+)-Batzelladine A an

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## Abstract Asymmetric total synthesis of batzelladine A (**1**) and batzelladine D (**2**) has been achieved. Our synthesis of batzelladines features 1) stereoselective construction of the cyclic guanidine system by means of successive 1,3‐dipolar cycloaddition reaction and subsequent cyclization,