Literature DB >> 30666326

Recent development on the [5+2] cycloadditions and their application in natural product synthesis.

Kai Gao1, Yong-Gang Zhang, Zhiming Wang, Hanfeng Ding.   

Abstract

The [5+2] cycloaddition is one kind of fascinating and powerful reaction to access seven-membered ring systems existing in complex natural products and pharmaceuticals. In this review, recent developments on the [5+2] cycloadditions and their application in the synthesis of complex natural products are discussed. A focus is given to the way in which the [5+2] cycloadditions have influenced the logical process of the synthesis. This article is organized by reaction types, aiming to provide a clear clue to the latest research trends.

Year:  2019        PMID: 30666326     DOI: 10.1039/c8cc09077g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

Review 1.  Natural Product Synthesis Enabled by Domino Processes Incorporating a 1,2-Rearrangement Step.

Authors:  Bastien Delayre; Qian Wang; Jieping Zhu
Journal:  ACS Cent Sci       Date:  2021-04-08       Impact factor: 14.553

2.  Highly Diastereoselective Intramolecular Asymmetric Oxidopyrylium-olefin [5 + 2] Cycloaddition and Synthesis of 8-Oxabicyclo[3.2.1]oct-3-enone Containing Ring Systems.

Authors:  Arun K Ghosh; Monika Yadav
Journal:  J Org Chem       Date:  2021-05-20       Impact factor: 4.198

3.  Synthesis of Polycyclic Ether-Benzopyrans and In Vitro Inhibitory Activity against Leishmania tarentolae.

Authors:  Sarita Singh; Jacob P Grabowski; Shilpa Pohani; C Fiore Apuzzo; David C Platt; Marjorie A Jones; T Andrew Mitchell
Journal:  Molecules       Date:  2020-11-21       Impact factor: 4.411

4.  Intermolecular [5+2] Annulation between 1-Indanones and Internal Alkynes by Rhodium-Catalyzed C-C Activation.

Authors:  Rui Zhang; Ying Xia; Guangbin Dong
Journal:  Angew Chem Int Ed Engl       Date:  2021-08-03       Impact factor: 16.823

  4 in total

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