Skip to main content

Research Repository

Advanced Search

Enhancing the potential of enantioselective organocatalysis with light

Melchiorre, Paolo; Silvi, Mattia

Enhancing the potential of enantioselective organocatalysis with light Thumbnail


Authors

Paolo Melchiorre



Abstract

© 2018 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. Organocatalysis - catalysis mediated by small chiral organic molecules - is a powerful technology for enantioselective synthesis, and has extensive applications in traditional ionic, two-electron-pair reactivity domains. Recently, organocatalysis has been successfully combined with photochemical reactivity to unlock previously inaccessible reaction pathways, thereby creating new synthetic opportunities. Here we describe the historical context, scientific reasoning and landmark discoveries that were essential in expanding the functions of organocatalysis to include one-electron-mediated chemistry and excited-state reactivity.

Citation

Melchiorre, P., & Silvi, M. (2018). Enhancing the potential of enantioselective organocatalysis with light. Nature, 554(7690), 41-49. https://doi.org/10.1038/nature25175

Journal Article Type Article
Acceptance Date Nov 24, 2017
Online Publication Date Feb 1, 2018
Publication Date 2018-02
Deposit Date Jan 29, 2020
Publicly Available Date Jan 31, 2020
Journal Nature
Print ISSN 0028-0836
Electronic ISSN 1476-4687
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 554
Issue 7690
Pages 41-49
DOI https://doi.org/10.1038/nature25175
Keywords Multidisciplinary
Public URL https://nottingham-repository.worktribe.com/output/3826615
Publisher URL https://www.nature.com/articles/nature25175
Additional Information Received: 8 August 2017; Accepted: 24 November 2017; First Online: 1 February 2018; : The authors declare no competing financial interests.

Files





You might also like



Downloadable Citations