Abstract:
13C-NMR spectra of deoxyaldonolactones, derived from L-rhamnose, are interpreted and discussed in terms of ring-size and substituents. It is shown that this spectroscopic method constitutes a useful tool in the structural determination of isomeric 1,4- and 1,5-lactones. © 1983.
Referencias:
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Citas:
---------- APA ----------
Cirelli, A.F., Sznaidman, M., Varela, O.J. & De Lederkremer, R.M.
(1983)
. Confirmation of the structure of aldonolactones by 13c-NMR. Tetrahedron, 39(2), 313-316.
http://dx.doi.org/10.1016/S0040-4020(01)91825-3---------- CHICAGO ----------
Cirelli, A.F., Sznaidman, M., Varela, O.J., De Lederkremer, R.M.
"Confirmation of the structure of aldonolactones by 13c-NMR"
. Tetrahedron 39, no. 2
(1983) : 313-316.
http://dx.doi.org/10.1016/S0040-4020(01)91825-3---------- MLA ----------
Cirelli, A.F., Sznaidman, M., Varela, O.J., De Lederkremer, R.M.
"Confirmation of the structure of aldonolactones by 13c-NMR"
. Tetrahedron, vol. 39, no. 2, 1983, pp. 313-316.
http://dx.doi.org/10.1016/S0040-4020(01)91825-3---------- VANCOUVER ----------
Cirelli, A.F., Sznaidman, M., Varela, O.J., De Lederkremer, R.M. Confirmation of the structure of aldonolactones by 13c-NMR. Tetrahedron. 1983;39(2):313-316.
http://dx.doi.org/10.1016/S0040-4020(01)91825-3