Literature DB >> 23470747

Concise total synthesis of acortatarin A.

Takaaki Teranishi1, Masayuki Kageyama, Shigefumi Kuwahara.   

Abstract

The spirocyclic pyrrole alkaloid, acortatarin A, which had been isolated from a Chinese medicinal plant, was synthesized from a known olefinic compound by a concise six-step sequence involving N-alkylation of a pyrrole derivative with an α-bromo ketone intermediate as the key step.

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Year:  2013        PMID: 23470747     DOI: 10.1271/bbb.120862

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  3 in total

1.  Stereocontrolled Synthesis of Spiroketals: An Engine for Chemical and Biological Discovery.

Authors:  Alyssa L Verano; Derek S Tan
Journal:  Isr J Chem       Date:  2017-03-10       Impact factor: 3.333

2.  Cascade N-Alkylation/Hemiacetalization for Facile Construction of the Spiroketal Skeleton of Acortatarin Alkaloids with Therapeutic Potentiality in Diabetic Nephropathy.

Authors:  Pei Cao; Zhen-Jie Li; Wen-Wu Sun; Shashwat Malhotra; Yuan-Liang Ma; Bin Wu; Virinder S Parmar
Journal:  Nat Prod Bioprospect       Date:  2014-12-16

3.  Family-level stereoselective synthesis and biological evaluation of pyrrolomorpholine spiroketal natural product antioxidants.

Authors:  Alyssa L Verano; Derek S Tan
Journal:  Chem Sci       Date:  2017-03-15       Impact factor: 9.825

  3 in total

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