Addition of Chloroprene Grignards to Aromatic Aldehydes: Synthesis of Homoallenyl Alcohols

被引:6
|
作者
Geissler, Arne G. A. [1 ]
Breit, Bernhard [1 ]
机构
[1] Albert Ludwigs Univ Freiburg, Inst Organ Chem, D-79104 Freiburg, Germany
关键词
ALLYLIC ALKYLATION; EFFICIENT SYNTHESIS; CONJUGATE ADDITION; REAGENTS; ALLENES; NUCLEOPHILES; MECHANISM; METAL;
D O I
10.1021/acs.orglett.1c00527
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A general procedure for the one-pot synthesis of racemic homoallenyl alcohols from the corresponding aldehyde and chloroprene-derived Grignards is described. Employing bis[2-dimethylaminoethyl]ether (BDMAEE) as an additive at low temperatures shifts the selectivity of the chloroprene Grignard addition to aldehydes such that it is almost exclusive toward allene formation. In a set of follow-up experiments, simple and more elaborate methods for further derivatization have been demonstrated, allowing quick access to more complex structures.
引用
收藏
页码:2621 / 2625
页数:5
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