“…94 This method displays excellent chemoselectivity and allows the highly selective reduction of amides in the presence of other unsaturated groups such as alkenes, nitriles, esters, ketones, and even aldehydes. Different N,N-substituted amides (111) were well reduced. The reduction efficiency was closely affected by the electronic properties of the aromatic rings of aromatic amides and the steric environment of the α-position of aliphatic amides.…”
Section: Reduction Of Amidesmentioning
confidence: 98%
“…The synthetic practicability of this modified McFadyen-Stevens reaction was further emphasized by Shimokawa. 111…”
The reductive synthesis of aldehydes from carboxylic acids and their derivatives without the formation of alkanol intermediates, in a redox-economic fashion, is synthetically very intriguing yet practically very challenging. Recent...
“…94 This method displays excellent chemoselectivity and allows the highly selective reduction of amides in the presence of other unsaturated groups such as alkenes, nitriles, esters, ketones, and even aldehydes. Different N,N-substituted amides (111) were well reduced. The reduction efficiency was closely affected by the electronic properties of the aromatic rings of aromatic amides and the steric environment of the α-position of aliphatic amides.…”
Section: Reduction Of Amidesmentioning
confidence: 98%
“…The synthetic practicability of this modified McFadyen-Stevens reaction was further emphasized by Shimokawa. 111…”
The reductive synthesis of aldehydes from carboxylic acids and their derivatives without the formation of alkanol intermediates, in a redox-economic fashion, is synthetically very intriguing yet practically very challenging. Recent...
Under mild conditions, an N-phthalimidoyl sulfoximine undergoes aminolysis to provide a wide range of 2-formyl benzamides in good to high yields. An unprecedented variant of McFadyen-Stevens reaction explains the product formation. The applicability of the products as building blocks for nitriles and alkynes has been demonstrated.
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