N-N Bond Formation Using an Iodonitrene as an Umpolung of Ammonia: Straightforward and Chemoselective Synthesis of Hydrazinium Salts

被引:22
|
作者
Tota, Arianna [1 ]
Colella, Marco [1 ]
Carlucci, Claudia [1 ]
Aramini, Andrea [2 ]
Clarkson, Guy [3 ]
Degennaro, Leonardo [1 ]
Bull, James A. [4 ]
Luisi, Renzo [1 ]
机构
[1] Univ Bari A Moro, Dept Pharm Drug Sci, Via E Orabona 4, I-70125 Bari, Italy
[2] Dompe Farmaceut SpA, Dept Discovery, Via Campo Pile, I-67100 Laquila, Italy
[3] Univ Warwick, Dept Chem, Gibbet Hill Rd, Coventry CV4 7AL, W Midlands, England
[4] Imperial Coll London, Dept Chem, Mol Sci Res Hub, White City Campus,Wood Lane, London W12 0BZ, England
基金
欧盟地平线“2020”;
关键词
Hydrazinium Salts; Electrophilic Nitrogen; Nitrene; Hypervalent Iodine; Amines; O-TRANSFER; ELECTROPHILIC AMINATION; TERTIARY-AMINES; SULFOXIMINES; AMIDRAZONES; RECEPTOR; IODINE; PB28;
D O I
10.1002/adsc.202001047
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The formation of hydrazinium salts by N-N bond formation has typically involved the use of hazardous and difficult to handle reagents. Here, mild and operationally simple conditions for the synthesis of hydrazinium salts are reported. Electrophilic nitrogen transfer to the nitrogen atom of tertiary amines is achieved using iodosylbenzene as oxidant and ammonium carbamate as the N-source. The resulting process is highly chemoselective and tolerant to other functional groups. A wide scope is reported, including examples with bioactive molecules. Insights on the structure of hydrazinium salts were provided by X-ray analysis.
引用
收藏
页码:194 / 199
页数:6
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