Referencias:
- Bradley, W., Robinson, R., (1928) J. Chem. Soc., p. 1541
- Anderson, R.J., Nabenhauer, F.P., (1926) J. Am. Chem. Soc., 48, p. 2997
- Bogert, M.T., Coyne, B.B., (1929) J. Am. Chem. Soc., 51, p. 569
- Melting points are uncorrected. Except where stated otherwise, UV spectra were determined with a Beckman DK-2 instrument for solutions in ethanol; log ε follows λmax · IR were recorded on a Perkin-Elmer 137-B Infracord spectrophotometer as suspensions in Nujo1. Nmr spectra were obtained in a Varian A60 spectrometer with TMS as internal reference. Tlc were performed in silica gel plates; solvent; benzene-dioxane-acetic acid, 95:25:4 using acetic acid: Oleum, 80:20 and heat as reagent
Citas:
---------- APA ----------
Sotelo, R.M., Giacopello, D. & Vernengo, M.J.
(1972)
. 2-nitrohomosyringic acid. Organic Preparations and Procedures International, 4(6), 293-296.
http://dx.doi.org/10.1080/00304947209458280---------- CHICAGO ----------
Sotelo, R.M., Giacopello, D., Vernengo, M.J.
"2-nitrohomosyringic acid"
. Organic Preparations and Procedures International 4, no. 6
(1972) : 293-296.
http://dx.doi.org/10.1080/00304947209458280---------- MLA ----------
Sotelo, R.M., Giacopello, D., Vernengo, M.J.
"2-nitrohomosyringic acid"
. Organic Preparations and Procedures International, vol. 4, no. 6, 1972, pp. 293-296.
http://dx.doi.org/10.1080/00304947209458280---------- VANCOUVER ----------
Sotelo, R.M., Giacopello, D., Vernengo, M.J. 2-nitrohomosyringic acid. Org. Prep. Proc. Int. 1972;4(6):293-296.
http://dx.doi.org/10.1080/00304947209458280