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Herein, we report the development of a highly enantioselective aminoallylation reaction of both aldehyde and ketone electrophiles through the Cu-catalyzed reductive coupling of N-substituted allenes (allenamides). Through optimization of the allenami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2340272d9fdcf119f6c895572357b7f1
https://doi.org/10.26434/chemrxiv-2022-94pg8
https://doi.org/10.26434/chemrxiv-2022-94pg8
Asymmetric Access to Boryl-Substituted Vicinal Aminoalcohols through Cu-Catalyzed Reductive Coupling
Autor:
Samantha Gargaro, Joshua Sieber
Important biologically active organic compounds such as natural products and pharmaceuticals often contain multiple oxygen and nitrogen heteroatoms within their carbon framework. Furthermore, chiral 1,2-aminoalcohol substitution patterns are often pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cd31181483eaae000b2a1ebc737dd7a
https://doi.org/10.26434/chemrxiv-2022-lmkp8
https://doi.org/10.26434/chemrxiv-2022-lmkp8
The development of an asymmetric protocol for the reductive alkynylation of amides to access important alfa-chiral tertiary propargylic amines is reported using tandem Ir-catalyzed hydrosilylation/enantioselective Cu-catalyzed alkynylation. The react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06da8bd00feaede3f0359abee57f2ec7
https://doi.org/10.26434/chemrxiv-2021-9fhcr
https://doi.org/10.26434/chemrxiv-2021-9fhcr