Organocatalytic Asymmetric Tandem Michael Addition-Hemiacetalization: A Route to Chiral Dihydrocoumarins, Chromanes, and 4H-Chromenes
Organocatalytic Asymmetric Tandem Michael Addition-Hemiacetalization: A Route to Chiral Dihydrocoumarins, Chromanes, and 4H-Chromenes
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有机催化不对称串联迈克尔加成-半缩醛化:制备手性二氢香豆素、色满和 4H-色烯的途径
DOI:
10.1021/jo101446d
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发表时间:
2010-10-15
影响因子:
3.6
通讯作者:
Gong, Yuefa
中科院分区:
文献类型:
--
作者:
Lu, Dengfu;Li, Yajun;Gong, Yuefa
Asymmetric tandem Michael addition -hemacetalization between aliphatic aldehydes and (L)-2-(2-nitiovinyl)phenols was investigated for constructing benzopyran backbones. Interestingly. the diastereo- and enantioselectivities changed markedly when the reaction was mediated by different types of secondary amine catalysts The diphenylprolinol silyl ether 7 promoted the reaction with excellent enantioselectivitics (up to 99% cc) hut with model ate diastereoselectivitics (2 8 1 to 10) Prolylprolinols are another type of efficient catalyst Among them. L,L-prolylprolimol 5c is identified as the optimal species. showing high catalytic activity. good enantioselectivities (up to 89% ee). and excellent diasereoselectivities (up to 50 1 dt) Various aliphatic aldehydes and substituted (L)-2-(2-nitrovinyl)phenols were proven to he well tolerated in this tandem reaction In addition the chroman-2-ols 3 yielded in the above reactions could he conveniently transformed to synthetically and biologically significant chiral dihydrocoumarin chroman. and 4H-chromene derivatives