-
1
-
-
0001132655
-
H. Efficient deprotection of phenol methoxymethyl ethers using a solid acid catalyst with wells- dawson structure
-
DOI:10.3390/61201006
-
Romanelli, G., Autino J. C., Baronetti, G. & Thomas, H. (2001). H. Efficient Deprotection of Phenol Methoxymethyl Ethers Using a Solid Acid Catalyst with Wells- Dawson Structure. Molecules. 6, 1006 - 1011. DOI:10.3390/ 61201006.
-
(2001)
Molecules
, vol.6
, pp. 1006-1011
-
-
Romanelli, G.1
Autino, J.C.2
Baronetti, G.3
Thomas, H.4
-
2
-
-
38349062068
-
Advances in Catalysis
-
Okuhara, T., Mizuno, N. & Misono, M. (1996). Advances in Catalysis. Catalytic Chemistry of Heteropoly compounds. 41, 113-252.
-
(1996)
Catalytic Chemistry of Heteropoly Compounds
, vol.41
, pp. 113-252
-
-
Okuhara, T.1
Mizuno, N.2
Misono, M.3
-
3
-
-
77649238861
-
Advances in catalysis by heteropoly acids. Advances in catalysis by heteropoly acids
-
DOI:10.1070/RC1987v056n09ABEH003304
-
Kozhevnikov, I. V.(1987). Advances in catalysis by heteropoly acids. Advances in catalysis by heteropoly acids. Russ. Chem. Rev. 56(9), 811-825. DOI: 10.1070/RC1987v056n09ABEH003304.
-
(1987)
Russ. Chem. Rev.
, vol.56
, Issue.9
, pp. 811-825
-
-
Kozhevnikov, I.V.1
-
4
-
-
0035594725
-
The Chemistry of Isatins: A Review from 1975 to 1999
-
DOI:10.1590/S0103-50532001000300002
-
Joaquim, F. M., Simon, J. G. & Angelo, C. P. (2001). The Chemistry of Isatins: a Review from 1975 to 1999. Braz. Chem. Soc. 12 (3), 273 - 324. DOI: 10.1590/S0103- 50532001000300002.
-
(2001)
Braz. Chem. Soc.
, vol.12
, Issue.3
, pp. 273-324
-
-
Joaquim, F.M.1
Simon, J.G.2
Angelo, C.P.3
-
5
-
-
0000209043
-
The structure and properties of some indolic constituents in Couroupita guianensis aubl
-
DOI:10.1016/S0040-4020(01)96609-8
-
Bergman, J., Lindström, J. O. & Tilstam, U. (1985). The structure and properties of some indolic constituents in Couroupita guianensis aubl. Tetrahedron. 41 (14), 2879-2881. DOI:10.1016/S0040-4020(01)96609-8.
-
(1985)
Tetrahedron
, vol.41
, Issue.14
, pp. 2879-2881
-
-
Bergman, J.1
Lindström, J.O.2
Tilstam, U.3
-
6
-
-
0011740876
-
The melosatins a novel class of alkaloids from melochia tomentosa
-
DOI:10.1016/0040-4020(80)80221-3
-
Kapadia, G. J., Shukla, Y. N., Basak, S. P., Sokoloski, E. A. & Fales, H. M. (1980). The melosatins a novel class of alkaloids from melochia tomentosa. Tetrahedron. 36, 2441-2447. DOI:10.1016/0040-4020(80)80221-3.
-
(1980)
Tetrahedron
, vol.36
, pp. 2441-2447
-
-
Kapadia, G.J.1
Shukla, Y.N.2
Basak, S.P.3
Sokoloski, E.A.4
Fales, H.M.5
-
7
-
-
0038461872
-
Sporidesmins. Part II. the structure of degradation products related to 5-chloro-6,7-dimethoxyisatin
-
DOI:10.1039/JR9630005332
-
Hodges, R. J., Ronaldson, W., Taylor, A. & White, E. P. (1963). Sporidesmins. Part II. The structure of degradation products related to 5-chloro-6,7-dimethoxyisatin. J. Chem. Soc. 5332-5336. DOI: 10.1039/ JR9630005332.
-
(1963)
J. Chem. Soc.
, pp. 5332-5336
-
-
Hodges, R.J.1
Ronaldson, W.2
Taylor, A.3
White, E.P.4
-
8
-
-
37049171600
-
6: 7-Dimethoxyisatin, 5 : 6tin, and the nuclear degradation of 3: 4-methylenedioxyquindoline
-
DOI:10.1039/JR9290002924
-
Gulland, J. M., Robinson, R., Scott, J. & Thornley, S. (1929). 6: 7-Dimethoxyisatin, 5 : 6-methylenedioxyisatin, and the nuclear degradation of 3: 4-methylenedioxyquindoline. J. Chem. Soc. 2924-2927. DOI: 10.1039/JR9290002924.
-
(1929)
J. Chem. Soc.
, pp. 2924-2927
-
-
Gulland, J.M.1
Robinson, R.2
Scott, J.3
Thornley, S.4
-
9
-
-
33646493505
-
A catalytic method for synthesis of ?-butyrolactone, ?-caprolactone and 2-cumaranone in the presence of Preyssler's anion, [NaP5W30O110]14-, as a green and reusable catalyst
-
DOI:10.1016/j.molcata.2006.01.067
-
Bamoharram, F. F., Heravi, M. M., Roshani, M., Gharib, A. & Jahangir, M. (2006). A catalytic method for synthesis of ?-butyrolactone, ?-caprolactone and 2-cumaranone in the presence of Preyssler's anion, [NaP5W30O110]14-, as a green and reusable catalyst. J. Mol. Catal. 252, 90-95. DOI:10.1016/j.molcata. 2006.01.067.
-
(2006)
J. Mol. Catal.
, vol.252
, pp. 90-95
-
-
Bamoharram, F.F.1
Heravi, M.M.2
Roshani, M.3
Gharib, A.4
Jahangir, M.5
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