Manganese catalysed enantioselective hydrogenation of<i>in situ</i>-synthesised imines: efficient asymmetric synthesis of amino-indane derivatives-Reference-Cited by-同舟云学术

Manganese catalysed enantioselective hydrogenation ofin situ-synthesised imines: efficient asymmetric synthesis of amino-indane derivatives

Published:2023 Issue:10 Volume:25 Page:3864-3868
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Oates Conor L.¹,Goodfellow Alister S.¹^ORCID,Bühl Michael¹^ORCID,Clarke Matthew L.¹^ORCID

Affiliation:

1. School of Chemistry, University of St Andrews, EaSTCHEM, St Andrews, Fife, KY16 9ST, UK

Abstract

Indanone derivatives can be directly converted to amino-indanes with high enantioselectivity using a manganese catalyst. Selectivity can be rationalised by DFT calculations.

Funder

University of St Andrews

Engineering and Physical Sciences Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/GC/D3GC00399J

Reference41 articles.

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5. Enantioselective Hydrogenation of Activated Aryl Imines Catalyzed by an Iron(II) P-NH-P′ Complex

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