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Phosphine catalysed (5 + 1) annulation of ynone/cinnamates with primary amines
Chemical Communications ( IF 4.9 ) Pub Date : 2017-11-10 00:00:00 , DOI: 10.1039/c7cc08252e
Jhi Ametovski 1, 2, 3, 4, 5 , Uttam Dutta 1, 2, 3, 4, 5 , Laura Burchill 1, 2, 3, 4, 5 , Debabrata Maiti 6, 7, 8, 9 , David W. Lupton 1, 2, 3, 4, 5 , Joel F. Hooper 1, 2, 3, 4, 5
Affiliation  

The (5 + 1) annulation of ynone/cinnamates and related substrates with protected primary amines gives rise to isoquinolones, pyrrolidinones and pyrrolopiperazines in good to excellent yields under phosphine catalysis. The reaction is viable with chiral phosphines, although the selectivity is poor.

中文翻译:

膦与伯胺催化(5 +1)的乙炔/肉桂酸环化反应

炔酮/肉桂酸酯和相关底物与受保护的伯胺的(5 +1)环化反应会在膦催化下以优异的产率产生异喹诺酮,吡咯烷酮和吡咯烷哌嗪。尽管选择性差,但是该反应对于手性膦是可行的。
更新日期:2017-11-22
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