Journal
CHEMICAL COMMUNICATIONS
Volume 53, Issue 18, Pages 2768-2771Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6cc09775h
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Funding
- NSFC [21372002, 21232007]
- PAPD
- Natural Science Foundation of Jiangsu Province [BK20160003]
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The first [4+ 3] cycloaddition of ortho-hydroxybenzyl alcohols has been established by making use of N, N'-cyclic azomethine imines as suitable 1,3-dipoles under Bronsted acid catalysis. By using this strategy, biologically important seven-membered heterocyclic scaffolds have been constructed in good yields and excellent diastereoselectivities (up to 92% yield, most 495 : 5 dr).
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