Photoredox-Catalyzed Four-Component Reaction for the Synthesis of Complex Secondary Amines Full article
Journal |
Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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Output data | Year: 2020, Volume: 22, Number: 9, Pages: 3318-3322 Pages count : 5 DOI: 10.1021/acs.orglett.0c00614 | ||||
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Abstract:
The one-pot sulfonylation/aminoalkylation of styrene derivatives furnishing substituted γ-sulfonylamines was accomplished through a photoredox-catalyzed four-component reaction. Besides one molecule of water and the sodium counterion of the sulfinate, all atoms of the starting materials are transferred to the final product, rendering this process highly atom-efficient. The operationally simple protocol allows for the simultaneous formation of three new single bonds (C–S, C–N, and C–C) and therefore grants rapid access to structurally diverse products.
Cite:
Kammer L.M.
, Krumb M.
, Spitzbarth B.
, Lipp B.
, Kühlborn J.
, Busold J.
, Olga M Mulina
, Alexander O Terentev
, Opatz T.
Photoredox-Catalyzed Four-Component Reaction for the Synthesis of Complex Secondary Amines
Organic Letters. 2020. V.22. N9. P.3318-3322. DOI: 10.1021/acs.orglett.0c00614 WOS Scopus OpenAlex
Photoredox-Catalyzed Four-Component Reaction for the Synthesis of Complex Secondary Amines
Organic Letters. 2020. V.22. N9. P.3318-3322. DOI: 10.1021/acs.orglett.0c00614 WOS Scopus OpenAlex
Identifiers:
Web of science: | WOS:000530076400004 |
Scopus: | 2-s2.0-85081962909 |
OpenAlex: | W3010911651 |