Knoevenagel Condensation of Phosphinoylacetic Acids with Aldehydes: An Efficient One-Pot Strategy for the Synthesis of P-Functionalized Alkenyl Compounds

被引:8
作者
Dziuba, Kamil [1 ]
Frynas, Slawomir [1 ]
Szwaczko, Katarzyna [1 ]
机构
[1] Marie Curie Sklodowska Univ, Fac Chem, Inst Chem Sci, Dept Organ Chem, Gliniana St 33, PL-20614 Lublin, Poland
来源
SYNTHESIS-STUTTGART | 2021年 / 53卷 / 12期
关键词
Knoevenagel condensation; alkenylphosphine oxide; phosphinoylacetic acid; amine; acid-catalyzed; metal free; PHOSPHINE OXIDES; CATALYZED HYDROPHOSPHORYLATION; DIPHENYLPHOSPHINE OXIDE; INTERMOLECULAR HYDROPHOSPHINATION; STEREOSELECTIVE ADDITION; TRANSFER HYDROGENATION; OXIDATIVE ADDITION; TERMINAL ALKYNES; BOND FORMATION; PALLADIUM;
D O I
10.1055/s-0040-1705993
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A wide range of commercially available aldehydes have been applied to Knoevenagel condensation reaction to give E-alkenylphosphine oxides and vinylphosphine oxides. The readily available phosphinoylacetic acids derived from P(O)-H compounds were used as the starting materials in the reaction, providing a highly stereoselective and efficient method for constructing alpha,beta-unsaturated phosphine oxides. Moreover, this simple and practical procedure provides an alternative and more environmentally friendly synthesis strategy for this type of P-functionalized alkenyl compounds.
引用
收藏
页码:2142 / 2154
页数:13
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