Literature DB >> 25017898

Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products.

Minghao Feng1, Xuefeng Jiang.   

Abstract

An asymmetric synthetic strategy for constructing the divergent-synthesis monomer of epidithiodiketopiperazine (ETP) natural products has been successfully developed. The functionalized 2,3,3a,4,7,7a-hexahydroindole scaffold was constructed by a diastereoselective inverse electron-demand Diels-Alder (IEDDA) reaction.

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Year:  2014        PMID： 25017898     DOI： 10.1039/c4cc04148h

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


  4 in total

1.  Enantioselective construction of cis-hydroindole scaffolds via an asymmetric inverse-electron-demand Diels-Alder reaction: application to the formal total synthesis of (+)-minovincine.

Authors:  Fangqing Zhang; Bing-Tao Ren; Yuqiao Zhou; Yangbin Liu; Xiaoming Feng
Journal:  Chem Sci       Date:  2022-04-15       Impact factor: 9.969

2.  Enantioselective Synthesis of (-)-Acetylapoaranotin.

Authors:  Haoxuan Wang; Clinton J Regan; Julian A Codelli; Paola Romanato; Angela L A Puchlopek-Dermenci; Sarah E Reisman
Journal:  Org Lett       Date:  2017-03-28       Impact factor: 6.005

3.  tert-Butyl(2-oxo-2H-pyran-5-yl)carbamate as the First Chameleon Diene Bearing an Electron-Donating Substituent.

Authors:  Yasser M Omar; Giulia Santucci; Kamyar Afarinkia
Journal:  Molecules       Date:  2022-09-02       Impact factor: 4.927

4.  Direct Synthesis of Enamides via Electrophilic Activation of Amides.

Authors:  Philipp Spieß; Martin Berger; Daniel Kaiser; Nuno Maulide
Journal:  J Am Chem Soc       Date:  2021-07-07       Impact factor: 15.419
  4 in total

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