期刊
CHEMICAL COMMUNICATIONS
卷 49, 期 42, 页码 4752-4754出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc41409d
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资金
- University of Strasbourg
- CNRS
- Agence Nationale de la Recherche (ANR)
- Swiss National Science Foundation
The reaction of readily available optically active Si-tethered tris(malonates) with C-60 gave easily separable diastereoisomers differing by the absolute configuration of the inherently chiral addition pattern on the fullerene core. The absolute configuration of the e,e,e addition pattern has been unambiguously determined using X-ray crystal structure analysis.
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