期刊
ORGANIC LETTERS
卷 14, 期 17, 页码 4537-4539出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol302042u
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资金
- Australian Research Council [DE120102113]
- Australian Research Council [DE120102113] Funding Source: Australian Research Council
The total synthesis of the racemic natural products (+/-)-incarviditone and (+/-)-incarvilleatone has been accomplished in three steps via biomimetic dimerization of (+/-)-rengyolone. Homochiral dimerization of (+/-)-rengyolone affords (+/-)-incarviditone through a domino oxa-Michael/Michael sequence. Heterochiral dimerization, involving a domino oxa-Michael/Michael/aldol reaction sequence, affords (+/-)-incarvilleatone. Single-crystal X-ray analysis of a derivative of (+/-)-incarviditone has resulted in revision of the originally proposed structure.
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