期刊
ORGANIC LETTERS
卷 12, 期 21, 页码 4812-4815出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol101969t
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资金
- National Science Council, ROC
A stereoselective synthesis of fully substituted cyclopentenes has been achieved by a sequential organocatalyzed Stetter and Michael-aldol condensation of aromatic aldehydes, nitroalkenes, and alpha,beta-unsaturated aldehydes via the [1 + 2 + 2] annulation strategy with excellent diastereoselectivities and enantioselectivities (up to >99% ee).
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