Synthesis of 1,2-oxazetidines with a free -NH group photoredox catalysis
A photoredox approach enabling one-step synthesis of oxazetidines with a free -NH group via the combined use of alkyne, thiophenol, and azide has been reported. The synthesized oxazetidine with the free -NH group was stable enough for various late-stage transformations such as methylation, acetylati...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2022-07, Vol.58 (61), p.858-8511 |
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container_title | Chemical communications (Cambridge, England) |
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creator | Ganie, Majid Ahmad Bhat, Muneer-Ul-Shafi Rizvi, Masood Ahmad Raheem, Shabnam Shah, Bhahwal Ali |
description | A photoredox approach enabling one-step synthesis of oxazetidines with a free -NH group
via
the combined use of alkyne, thiophenol, and azide has been reported. The synthesized oxazetidine with the free -NH group was stable enough for various late-stage transformations such as methylation, acetylation, tosylation, and ring-opening reaction to afford synthetically useful α-aminoketones.
A photoredox approach enabling one-step synthesis of oxazetidines with a free -NH group
via
the combined use of alkyne, thiophenol, and azide has been reported. |
doi_str_mv | 10.1039/d2cc02892a |
format | Article |
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via
the combined use of alkyne, thiophenol, and azide has been reported. The synthesized oxazetidine with the free -NH group was stable enough for various late-stage transformations such as methylation, acetylation, tosylation, and ring-opening reaction to afford synthetically useful α-aminoketones.
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via
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via
the combined use of alkyne, thiophenol, and azide has been reported. The synthesized oxazetidine with the free -NH group was stable enough for various late-stage transformations such as methylation, acetylation, tosylation, and ring-opening reaction to afford synthetically useful α-aminoketones.
A photoredox approach enabling one-step synthesis of oxazetidines with a free -NH group
via
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via
the combined use of alkyne, thiophenol, and azide has been reported. The synthesized oxazetidine with the free -NH group was stable enough for various late-stage transformations such as methylation, acetylation, tosylation, and ring-opening reaction to afford synthetically useful α-aminoketones.
A photoredox approach enabling one-step synthesis of oxazetidines with a free -NH group
via
the combined use of alkyne, thiophenol, and azide has been reported.</abstract><doi>10.1039/d2cc02892a</doi><tpages>4</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Synthesis of 1,2-oxazetidines with a free -NH group photoredox catalysis |
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