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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.
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页码:2621 / 2625
页数:5
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