O-nucleophilic amino alcohol acyl-transfer catalysts: the effect of acidity of the hydroxyl group on the activity of the catalyst.

O-nucleophilic amino alcohol acyl-transfer catalysts: the effect of acidity of the hydroxyl group on the activity of the catalyst.
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O-亲核氨基醇酰基转移催化剂:羟基的酸性对催化剂活性的影响。

DOI:
10.1021/ol035510n
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发表时间:
2003
期刊:
Organic letters.
影响因子:
--
通讯作者:
Sammakia,Tarek
Sammakia,Tarek
中科院分区:
--
文献类型:
--
作者:
Wayman,KjirstenA;Sammakia,Tarek

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氨基醇衍生的酰基转移催化剂以亲核机理起作用,羟基附近有吸电子基团的催化剂活性更强。这是由于催化剂羟基的酸度增加。
Amino alcohol-derived acyl-transfer catalysts are shown to operate by anO-nucleophilic mechanism, and catalysts bearing electron-withdrawing groups in proximity to the hydroxyl group are found to be more active. This is attributed to an increase in the acidity of the hydroxyl group of the catalyst.