R)-2-tert-Butyl-6-[(4R,5S)-3-iso­propyl-4-methyl-5-phenyl­oxazolidin-2-yl]phenol
[Figure 2]
[Figure 2]

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Figure 2 . The enhanced Jmol figure of the title compound. The intra­molecular H-bonding is highlighted as one of the radiobuttons. This is the first in a series of three Jmol figures intended to illustrate some versatility of the program. See also: Campbell et al. (2010); Anderson et al. (2010). In this Jmol, all inter­active features are defined by using the graphical inter­face. Some script artifacts occur and can only be remedied by hand-editing the scripts.





Highlight N3 substituent
Highlight C18 and substituent
Highlight C20 and substituent
Highlight none











This is the first in a series of three Jmol figures intended to illustrate some versatility of the program. In this Jmol, all interactive features are defined by using the graphical interface. Some script artifacts occur and can only be remedied by hand-editing the scripts.

Figure 2 . The enhanced Jmol figure of the title compound. The intra­molecular H-bonding is highlighted as one of the radiobuttons. This is the first in a series of three Jmol figures intended to illustrate some versatility of the program. See also: Campbell et al. (2010); Anderson et al. (2010). In this Jmol, all inter­active features are defined by using the graphical inter­face. Some script artifacts occur and can only be remedied by hand-editing the scripts.

Journal logo CRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 66| Part 4| March 2010| Pages o898-o899
doi:10.1107/S1600536810009591
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