Literature DB >> 32833268

Total Synthesis of Kopsinitarine E.

Karre Nagaraju1, Dongshun Ni1, Dawei Ma1.   

Abstract

Kopsinitarines A-E are complex octacyclic caged Kopsia alkaloids with strained cage skeletons and a unique cyclic hemiaminal bridge that makes total synthesis challenging. Herein, we disclose the first total synthesis of kopsinitarine E. The key synthetic features include a SmI2 -mediated radical cascade cyclization and a subsequent semi-pinacol rearrangement to install the key carbocyclic skeleton, a chemoselective hydrosilyl amide reduction to construct the hemiaminal ether bridge, and an intramolecular Mannich reaction to establish the highly strained cage system.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  Mannich reaction; cyclization; indole alkaloids; semi-pinacol rearrangement; total synthesis

Mesh:

Year:  2020        PMID: 32833268     DOI: 10.1002/anie.202011093

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


  2 in total

Review 1.  Samarium(ii) iodide-mediated reactions applied to natural product total synthesis.

Authors:  Majid M Heravi; Azadeh Nazari
Journal:  RSC Adv       Date:  2022-03-30       Impact factor: 3.361

Review 2.  Recent development and applications of semipinacol rearrangement reactions.

Authors:  Xiao-Ming Zhang; Bao-Sheng Li; Shao-Hua Wang; Kun Zhang; Fu-Min Zhang; Yong-Qiang Tu
Journal:  Chem Sci       Date:  2021-06-28       Impact factor: 9.825

  2 in total

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