期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 16, 期 2, 页码 262-265出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob02609a
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资金
- CSIR-INDIA [02 (0209)/14/EMR-II]
- IIT Madras, Chennai
An efficient formal total synthesis of two compounds from the selaginpulvilin family of natural products, selaginpulvilin A and C, has been successfully achieved. The tetradehydro Diels-Alder (TDDA) reaction between an enyne and alkyne has been utilized for the creation of the necessary fluorene skeleton. Attempts at the conversion of selaginpulvilin A to selaginpulvilin B, F and H were unsuccessful.
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