Chemical Data Collections, Год журнала: 2024, Номер unknown, С. 101164 - 101164
Опубликована: Сен. 1, 2024
Язык: Английский
Chemical Data Collections, Год журнала: 2024, Номер unknown, С. 101164 - 101164
Опубликована: Сен. 1, 2024
Язык: Английский
Chemical Science, Год журнала: 2024, Номер 15(16), С. 6012 - 6021
Опубликована: Янв. 1, 2024
A highly stereo- and chemoselective intermolecular coupling of diverse heterocycles with dialkynylphosphine oxides has been realized
Язык: Английский
Процитировано
2Chemical Communications, Год журнала: 2024, Номер unknown
Опубликована: Янв. 1, 2024
This review outlines methods and strategies to exploit specific azide positions for molecular conjugation in the presence of multiple azido groups. Illustrative examples spanning di-, tri- tetraazide click scaffolds are included.
Язык: Английский
Процитировано
2Опубликована: Фев. 9, 2024
A one-pot conversion of alkyl azides to diazo compounds is outlined. After azido group protection α-azidocarbonyl compounds, treatment the resulting phosphazides with silica gel in a wet solvent afforded α-diazo carbonyl products by azide-deprotective conversion. Competitive reactions α-azido amides and aryl demonstrate azide-site selectivity. Azide-site selective click functionalization this sequence also demonstrated diazido compounds.
Язык: Английский
Процитировано
1Organic Letters, Год журнала: 2024, Номер 26(12), С. 2409 - 2413
Опубликована: Март 19, 2024
A one-pot conversion of alkyl azides to diazo compounds is outlined. After the reaction α-azidocarbonyl with Amphos, treatment resulting phosphazides silica gel in a wet solvent afforded α-diazo carbonyl products. Through azido group protection property inter- and intramolecular azide-site selective reactions protection, click functionalization, deprotection have been demonstrated one pot.
Язык: Английский
Процитировано
1Chemical Data Collections, Год журнала: 2024, Номер unknown, С. 101164 - 101164
Опубликована: Сен. 1, 2024
Язык: Английский
Процитировано
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