3-Imidoallenylphosphonates: In Situ Formation and β-Alkoxylation

被引:13
作者
Berton, Jan K. E. T. [1 ]
Heugebaert, Thomas S. A. [1 ]
Debrouwer, Wouter [1 ]
Stevens, Christian V. [1 ]
机构
[1] Univ Ghent, Fac Biosci Engn, Dept Sustainable Organ Chem & Technol, SynBioC Res Grp, Coupure Links 653, B-9000 Ghent, Belgium
关键词
AMINO ALLENEPHOSPHONATES; PHOSPHITES; ALCOHOLS; ALKYNES; (DIMETHYLAMINO)ALLENE; HYDROAMINATION; REARRANGEMENT; NUCLEOPHILES; ALLENAMIDES; CYCLIZATION;
D O I
10.1021/acs.orglett.5b03314
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
3-Imidoallenylphosphonates, allenes bearing both an electron-withdrawing and -donating group, were isolated for the first time. An alkoxy substituent was introduced into these unprecedented intermediates in a one-pot approach, yielding beta-functionalized aminophosphonates in excellent yields and short reaction times. The mechanistic insights gained are important additions to the domain of allene chemistry. Addition of biologically important molecules, including monoglycerides, amino acids, and nucleosides, proves the general applicability of the developed method.
引用
收藏
页码:208 / 211
页数:4
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