Ph.D. THESIS ABSTRACT SYNTHESIS, STEREOCHEMISTRY AND ...
Ph.D. THESIS ABSTRACT SYNTHESIS, STEREOCHEMISTRY AND ...
Ph.D. THESIS ABSTRACT SYNTHESIS, STEREOCHEMISTRY AND ...
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Radu Gropeanu – <strong>Ph</strong>D Thesis Abstract<br />
7.5<br />
7.0<br />
6.5<br />
5'<br />
4'<br />
c<br />
6'<br />
6.0<br />
8<br />
2'<br />
b<br />
a<br />
CH3 H C 2<br />
9<br />
1<br />
N<br />
6<br />
5.5<br />
S<br />
O O<br />
d<br />
O O O O<br />
d<br />
e e e e e e<br />
Figure 5. 1 H-NMR spectrum of 44 (CDCl3, 300 MHz, r.t.)<br />
4<br />
2<br />
2'<br />
5.0<br />
6'<br />
c<br />
5'<br />
4'<br />
c<br />
4.5<br />
d<br />
a b<br />
In the aromatic area the signals were assigned studying the multiplicity, the shape and the<br />
coupling constants (Figure 6).<br />
H4, H6<br />
7.50<br />
20 20<br />
20<br />
H2, H8 H5'<br />
7.40<br />
CDCl 3<br />
7.30<br />
H2', H6'<br />
7.20<br />
41<br />
4.0<br />
5'<br />
4'<br />
c<br />
7.10<br />
6'<br />
8<br />
e<br />
3.5<br />
6<br />
S<br />
7.00<br />
3.0<br />
b<br />
a<br />
CH3 H2C 9<br />
1<br />
N<br />
O O<br />
d<br />
2'<br />
O O O O<br />
d<br />
e e e e e e<br />
H1, H9<br />
4<br />
2<br />
2'<br />
6'<br />
2.5<br />
c<br />
5'<br />
4'<br />
6.90<br />
2.0<br />
18 18<br />
Figure 6. Detail with the aromatic zone of the 1 H-NMR spectrum of 44 (CDCl3, 300 MHz, r.t.)<br />
The solid state molecular structure of 44 was determined by X-rays diffraction analysis of<br />
a monocrystal. In Figure 7 is presented the ORTEP drawing of one molecule.<br />
H4'<br />
1.5<br />
6.80<br />
33