User 677b9c22ff
23-12-2008 21:49:46
Hi,
sorry for possible double report, but I just put it in here.
I know there will be a major fix in v5.2.0.
This is a report from v5.1.0.
I used Xylitol as input (2R,3R,4S)-Pentane-1,2,3,4,5-pentol,
a) no stereoinformation OCC(O)C(O)C(O)CO
b) with some stereoinformation OC[C@H](O)[C@@H](O)[C@H](O)CO
In case a) I get three stereoisomers.
In case b) I get four stereoisomers.
Furthermore in case a) only two if the chiral centers are
created in case b) all three chiral centers are shown.
See attached picture
Tobias
sorry for possible double report, but I just put it in here.
I know there will be a major fix in v5.2.0.
This is a report from v5.1.0.
I used Xylitol as input (2R,3R,4S)-Pentane-1,2,3,4,5-pentol,
a) no stereoinformation OCC(O)C(O)C(O)CO
b) with some stereoinformation OC[C@H](O)[C@@H](O)[C@H](O)CO
In case a) I get three stereoisomers.
In case b) I get four stereoisomers.
Furthermore in case a) only two if the chiral centers are
created in case b) all three chiral centers are shown.
See attached picture
Tobias