期刊
ORGANIC LETTERS
卷 18, 期 11, 页码 2632-2635出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01030
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资金
- Max-Planck-Gesellschaft
The catalytic addition of the amino acid derived bifunctional N-acylaminophosphine to an alpha-substituted allene ester generated a zwitterionic dipole that engaged the vinylogous ester function of 3-cyano-chromones in a [4 + 2] annulation reaction to deliver tetrahydroxanthones embodying three consecutive chiral centers in high yields and with excellent enantioselectivities. The established asymmetric synthesis Anther paves the way to two different classes of complex, sp(3)-rich tetracyclic benzopyrans via efficient cascade reactions.
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