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Direct transformation of 2-acetylpyridine oxime esters into α-oxygenated imines in an Ir(III) complex
Dalton Transactions ( IF 4 ) Pub Date : 2017-08-24 00:00:00 , DOI: 10.1039/c7dt02528a
Hiroyuki Takahashi 1, 2, 3, 4, 5 , Shintaro Kodama 1, 2, 3, 4, 5 , Youichi Ishii 1, 2, 3, 4, 5
Affiliation  

2-Acetylpyridine oxime esters are transformed into the corresponding α-oxygenated imines in an Ir(III) complex under mild conditions, where the selective metal coordination of the imino group effectively promotes tautomerization of the oxime esters into the N-oxyenamines and the subsequent rearrangement.

中文翻译:

在Ir(III)配合物中将2-乙酰基吡啶肟酯直接转化为α-加氧的亚胺

在温和的条件下,将2-乙酰基吡啶肟肟酯转变为Ir(III)络合物中的相应α-加氧亚胺,其中亚氨基的选择性金属配位有效地促进了肟酯的互变异构成N-氧烯胺和随后的重排。
更新日期:2017-09-20
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