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Enantioselective organocatalytic hydride reduction
Stéphane G. Ouellet
, Jamison B. Tuttle
,
David W.C. MacMillan
Research output
:
Contribution to journal
›
Article
›
peer-review
485
Scopus citations
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Dive into the research topics of 'Enantioselective organocatalytic hydride reduction'. Together they form a unique fingerprint.
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Chemistry
Organocatalysis
100%
Hydrogen
33%
Isomerization
33%
Alkene
33%
Enal
33%
Ethyl
33%
Imidazolidinone
33%
Keyphrases
Olefins Removal
33%
Z-E Isomerization
33%
Impure
33%