期刊
ORGANIC LETTERS
卷 19, 期 20, 页码 5513-5516出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b02577
关键词
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资金
- NSFC [21232004, 21472123, 21620102003]
- STCSM [15JC1402200]
- SHMEC [201701070002E00030]
A one-step enantioselective and diastereqclivergent alpha-allylation unprotected alpha-hydroxy indanones has been developed using an Ir/Zn dual catalyst system; no additIonal base is required. The cyclic tertiary alpha-hydroxyketones containing vicinal stereocenters can be synthesized with excellent enantioselectivity (up to. >99% ee) and good diastereoselectiyity (up to 12:1,dr). By a simple choice of the appropriate chiral metal catalyst combination, all four product stereoisomers could be obtained from the same starling materials and under identical conditions.
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