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Nat Rev Chem
; 8(9): 647-648, 2024 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-39117757
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Nat Rev Chem
; 8(8): 564-565, 2024 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38886548
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Nat Rev Chem
; 8(6): 402-403, 2024 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38724648
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Nat Rev Chem
; 7(6): 379, 2023 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37237160
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Chem Commun (Camb)
; 58(35): 5387-5390, 2022 Apr 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35416220
RESUMO
Sulfonimidoyl halides have previously shown poor stability and selectivity in reaction with organometallic reagents. Here we report the preparation of enantioenriched sulfonimidoyl fluorides and their stereospecific reaction at sulfur with Grignard reagents. Notably the first enantioenriched alkyl sulfonimidoyl fluorides are prepared, including methyl. The nature of the N-group is important to the success of the stereocontrolled sequence to sulfoximines.
Assuntos
Fluoretos , Enxofre , Indicadores e Reagentes
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