Diastereoselective cyclization of a dithienylethene switch through single crystal confinement.
Diastereoselective cyclization of a dithienylethene switch through single crystal confinement.
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DOI:
10.1039/b517370a
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发表时间:
2006-03
影响因子:
3.2
通讯作者:
K. Uchida;M. Walko;J. D. de Jong;Shin-ichiro Sukata;S. Kobatake;A. Meetsma;J. V. van Esch;B. Feringa
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文献类型:
--
作者:
K. Uchida;M. Walko;J. D. de Jong;Shin-ichiro Sukata;S. Kobatake;A. Meetsma;J. V. van Esch;B. Feringa
Upon UV irradiation of the hydrogen-bond confined crystal state of a dithienylhexafluorocyclopentene with (R)-N-phenylethylamide substituents, the photochemical cyclization reaction proceeds diastereoselectively to form the coloured, closed-ring isomer with 97% de.