Literature DB >> 31184903

A Modular Construction of Epidithiodiketopiperazines.

Thomas N Snaddon1, Toya D Scaggs1, Colin M Pearson1, James W B Fyfe1.   

Abstract

Epidithiodiketopiperazines (ETPs) possess remarkably diverse biological activities and have attracted significant synthetic attention. The preparation of analogues is actively pursued; however, they are structurally challenging, and more direct and modular methods for their synthesis are desirable. To this end, the utility of a bifunctional triketopiperazine building block for the straightforward synthesis of ETPs is reported. A modular strategy consisting of enolate alkylation followed by site-selective nucleophile addition enables the concise synthesis of (±)-hyalodendrin and a range of analogues.

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Year:  2019        PMID: 31184903      PMCID: PMC7213270          DOI: 10.1021/acs.orglett.9b01770

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  44 in total

1.  A practical sulfenylation of 2,5-diketopiperazines.

Authors:  K C Nicolaou; Denis Giguère; Sotirios Totokotsopoulos; Ya-Ping Sun
Journal:  Angew Chem Int Ed Engl       Date:  2011-12-07       Impact factor: 15.336

2.  Chaetomin, a New Antibiotic Substance Produced by Chaetomium cochliodes: I. Formation and Properties.

Authors:  S A Waksman; E Bugie
Journal:  J Bacteriol       Date:  1944-11       Impact factor: 3.490

3.  Inactivation of rabbit muscle creatine kinase by reversible formation of an internal disulfide bond induced by the fungal toxin gliotoxin.

Authors:  A M Hurne; C L Chai; P Waring
Journal:  J Biol Chem       Date:  2000-08-18       Impact factor: 5.157

4.  Synthesis and biological evaluation of epidithio-, epitetrathio-, and bis-(methylthio)diketopiperazines: synthetic methodology, enantioselective total synthesis of epicoccin G, 8,8'-epi-ent-rostratin B, gliotoxin, gliotoxin G, emethallicin E, and haematocin and discovery of new antiviral and antimalarial agents.

Authors:  K C Nicolaou; Min Lu; Sotirios Totokotsopoulos; Philipp Heretsch; Denis Giguère; Ya-Ping Sun; David Sarlah; Thu H Nguyen; Ian C Wolf; Donald F Smee; Craig W Day; Selina Bopp; Elizabeth A Winzeler
Journal:  J Am Chem Soc       Date:  2012-10-04       Impact factor: 15.419

5.  Structural relationship of epipolythiodioxopiperazines and their immunomodulating activity.

Authors:  A Müllbacher; P Waring; U Tiwari-Palni; R D Eichner
Journal:  Mol Immunol       Date:  1986-02       Impact factor: 4.407

6.  Chaetocochins A-C, epipolythiodioxopiperazines from Chaetomium cochliodes.

Authors:  Guo-You Li; Bo-Gang Li; Tao Yang; Ju-Fang Yan; Guang-Ye Liu; Guo-Lin Zhang
Journal:  J Nat Prod       Date:  2006-09       Impact factor: 4.050

7.  Enantioselective total synthesis of (-)-acetylaranotin, a dihydrooxepine epidithiodiketopiperazine.

Authors:  Julian A Codelli; Angela L A Puchlopek; Sarah E Reisman
Journal:  J Am Chem Soc       Date:  2011-10-28       Impact factor: 15.419

8.  [[(tert-Butyl)dimethylsilyl]oxy]methyl group for sulfur protection.

Authors:  Lihong Wang; Derrick L J Clive
Journal:  Org Lett       Date:  2011-03-10       Impact factor: 6.005

Review 9.  Epidithiodioxopiperazines. occurrence, synthesis and biogenesis.

Authors:  Timothy R Welch; Robert M Williams
Journal:  Nat Prod Rep       Date:  2014-10       Impact factor: 13.423

10.  Studies on the mechanism of toxicity of the mycotoxin, sporidesmin. I. Generation of superoxide radical by sporidesmin.

Authors:  R Munday
Journal:  Chem Biol Interact       Date:  1982-09       Impact factor: 5.192

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  2 in total

1.  Synthesis of Potent Cytotoxic Epidithiodiketopiperazines Designed for Derivatization.

Authors:  Chase R Olsson; Joshua N Payette; Jaime H Cheah; Mohammad Movassaghi
Journal:  J Org Chem       Date:  2020-03-19       Impact factor: 4.354

2.  Total Synthesis of (-)-Glionitrin A and B Enabled by an Asymmetric Oxidative Sulfenylation of Triketopiperazines.

Authors:  Nicolas R Koning; Anders P Sundin; Daniel Strand
Journal:  J Am Chem Soc       Date:  2021-11-22       Impact factor: 15.419

  2 in total

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