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Synthesis 2022; 54(18): 4049-4058
DOI: 10.1055/a-1828-5837
DOI: 10.1055/a-1828-5837
paper
Total Synthesis of Chatenaytrienins-1, -3 and -4 and Muridienins-1–4 Enabled by C(sp)–C(sp3) Sonogashira Coupling
This work was supported by the Science and Engineering Research Board (SERB), New Delhi (Grant No. CRG/2021/000427). N.C. thanks the Council of Scientific and Industrial Research (CSIR), New Delhi for a research fellowship.
Abstract
Concise and efficient protecting-group-free total syntheses of chatenaytrienins-1, -3, -4 and muridienins-1–4 have been achieved. The key steps involve ring-closing metathesis (RCM) and C(sp)–C(sp3)-Sonogashira coupling. This work reports the first total syntheses of chatenaytrienin-3 and muridienins-1–4 in seven linear steps and high overall yields.
Key words
acetogenins - chatenaytrienins - muridienins - ring-closing metathesis - Sonogashira coupling - stereoselective synthesisSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-1828-5837.
- Supporting Information
Publication History
Received: 07 March 2022
Accepted after revision: 19 April 2022
Accepted Manuscript online:
19 April 2022
Article published online:
02 June 2022
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For selected reviews, see:
For recent reviews on the total synthesis of annonaceous acetogenins, see: