a-b-e-f-g-h-p-v-x
a-b-e-f-g-h-q-v-x
a-b-e-f-g-h-q-t-x
a-b-e-f-g-h-q-v-y
a-b-e-f-g-h-p-t-x
a-b-f-h-q-v-x
a-d-e-f-g-h-q-v-x
b-c-e-f-g-h-q-t-x
a-b-e-g-q-t-x
b-c-e-f-g-h-p-v-x
a-d-e-f-g-h-p-v-x
a-b-f-h-p-v-x
a-b-e-g-p-v-x
a-b-e-g-v-y
a-b-f-h-v-y
a-b-e-g-p-t-x
a-b-f-h-p-t-x
c-d-e-f-g-h-p-v-x
a-d-e-g-p-t-x
a-b-q-v-y
a-b-p-t-x
c-d-f-h-p-v-x
c-d-f-h-q-v-x
b-c-q-v-y
a-d-q-v-y
c-d-q-v-y
c-d-p-t-x
Fig. 3 Optimized geometries of representative conformers of jozimine A 2 and letter-combinations
identifying their characteristics in the acronyms denoting them. Geometries from HF/6-31G(d,p)
results. The images show the main combinations of interaction types and moieties’ orientations
which may be present in the conformers of jozimine A 2 . The initial part of the acronyms is not
reported under the images, because of space reasons; it is the same for all the conformers (JZM)
Computational Study of Jozimine A 2 , a Naphthylisoquinoline …
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