期刊
ORGANIC LETTERS
卷 7, 期 8, 页码 1453-1456出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol047347h
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资金
- NIGMS NIH HHS [NIGMS-54656] Funding Source: Medline
[GRAPHICS] Enantioselective radical alkylation of Baylis-Hillman adducts furnished aldol products in good yield and selectivity. The results illustrate that the selectivity in the hydrogen atom transfer is dependent on the size of the ester substituent, with smaller substituents providing better enantioselectivity.
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