Literature DB >> 27356738

A metal-catalyzed enyne-cyclization step for the synthesis of bi- and tricyclic scaffolds amenable to molecular library production.

Peng Wu1, Michael Åxman Petersen, A Emil Cohrt, Rico Petersen, Rémy Morgentin, Hugues Lemoine, Carine Roche, Anthony Willaume, Mads H Clausen, Thomas E Nielsen.   

Abstract

A facile metal-catalyzed diversification step for the synthesis of novel bi- and tricyclic scaffolds from enyne substrates is reported in this study. From a single starting material, topologically diverse scaffolds for library synthesis can be generated and decorated in a few steps. The methodology was used to produce a library of 490 compounds within the European Lead Factory (ELF) Consortium.

Entities:  

Year:  2016        PMID: 27356738     DOI: 10.1039/c6ob01148a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Highly Stereoselective Synthesis of a Compound Collection Based on the Bicyclic Scaffolds of Natural Products.

Authors:  Murali Annamalai; Stanimira Hristeva; Martyna Bielska; Raquel Ortega; Kamal Kumar
Journal:  Molecules       Date:  2017-05-18       Impact factor: 4.411

2.  Reactivity and Synthetic Applications of Multicomponent Petasis Reactions.

Authors:  Peng Wu; Michael Givskov; Thomas E Nielsen
Journal:  Chem Rev       Date:  2019-08-27       Impact factor: 60.622

  2 in total

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