-
1
-
-
84980120063
-
Formation of aldehydes and ketones from primary and secondary nitroalkanes, respectively, by treatment of their salts with sulfuric acid
-
(a) Nef, J. K. Formation of aldehydes and ketones from primary and secondary nitroalkanes, respectively, by treatment of their salts with sulfuric acid. Ann. Chem. 1894, 280, 263;
-
(1894)
Ann. Chem.
, vol.280
, pp. 263
-
-
Nef, J.K.1
-
2
-
-
0346339657
-
Recent synthetic developments in the nitro to carbonyl conversion Nef reaction
-
and references cited therein
-
(b) Ballini, R.; Petrini, M. Recent synthetic developments in the nitro to carbonyl conversion Nef reaction. Tetrahedron 2004, 60, 1017-1047 and references cited therein.
-
(2004)
Tetrahedron
, vol.60
, pp. 1017-1047
-
-
Ballini, R.1
Petrini, M.2
-
3
-
-
0000826393
-
Conversion of nitro paraffins into aldehydes and ketones
-
Kornblum, N.; Erickson, A. S.; Kelly, W. J.; Henggeler, B. Conversion of nitro paraffins into aldehydes and ketones. J. Org. Chem. 1982, 47, 4534-4538.
-
(1982)
J. Org. Chem.
, vol.47
, pp. 4534-4538
-
-
Kornblum, N.1
Erickson, A.S.2
Kelly, W.J.3
Henggeler, B.4
-
4
-
-
85077841429
-
Sodium borohydride reduction of nitrostyrenes by reverse addition: A simple and efficient method for the large-scale preparation of phenylnitroethanes
-
Bhattacharjya, A.; Mukhopadhyay, R.; Pakrashi, S. C. Sodium borohydride reduction of nitrostyrenes by reverse addition: a simple and efficient method for the large-scale preparation of phenylnitroethanes. Synthesis 1985, 886-887.
-
(1985)
Synthesis
, pp. 886-887
-
-
Bhattacharjya, A.1
Mukhopadhyay, R.2
Pakrashi, S.C.3
-
7
-
-
0001164738
-
Reduction of alpha, beta-unsaturated nitro compounds with boron hydrides: A new route to N-substituted hydroxylamines
-
Mourad, M. S.; Verma, R. S.; Kabalka, G. W. Reduction of alpha, beta-unsaturated nitro compounds with boron hydrides: a new route to N-substituted hydroxylamines. J. Org. Chem. 1985, 50, 133-135.
-
(1985)
J. Org. Chem.
, vol.50
, pp. 133-135
-
-
Mourad, M.S.1
Verma, R.S.2
Kabalka, G.W.3
-
8
-
-
84987065917
-
A simple unusual one step conversion of aromatic aldehydes into nitriles
-
Karmarkar, S. N.; Kelkar, S. L.; Wadia, M. S. A simple unusual one step conversion of aromatic aldehydes into nitriles. Synthesis 1985, 510-512.
-
(1985)
Synthesis
, pp. 510-512
-
-
Karmarkar, S.N.1
Kelkar, S.L.2
Wadia, M.S.3
-
9
-
-
0009739693
-
Reactions of vanillin and its derived compounds, XII: Benzyl methyl ketones derived from vanillin and its related compounds
-
Pearl, I. A.; Beyer, D. L. Reactions of vanillin and its derived compounds, XII: benzyl methyl ketones derived from vanillin and its related compounds. J. Org. Chem. 1951, 76, 221-224.
-
(1951)
J. Org. Chem.
, vol.76
, pp. 221-224
-
-
Pearl, I.A.1
Beyer, D.L.2
-
10
-
-
0001829128
-
The synthesis of ω-nitrostyrenes
-
Gairaud, C. B.; Lappin, G. R. The synthesis of ω-nitrostyrenes. J. Org. Chem. 1953, 18, 1-3.
-
(1953)
J. Org. Chem.
, vol.18
, pp. 1-3
-
-
Gairaud, C.B.1
Lappin, G.R.2
-
11
-
-
0001384404
-
Arylnitroalkenes: A new group of antibacterial agents
-
Schales, O.; Graefe, H. A. Arylnitroalkenes: a new group of antibacterial agents. J. Am. Chem. Soc. 1952, 74, 4486-4490.
-
(1952)
J. Am. Chem. Soc.
, vol.74
, pp. 4486-4490
-
-
Schales, O.1
Graefe, H.A.2
-
12
-
-
0039798534
-
A convenient synthesis of 1-(2-furyl)-2-nitroalk-1-enes on alumina surface without solvent
-
Rosini, G.; Ballini, R.; Petrini, M.; Sorrenti, P. A convenient synthesis of 1-(2-furyl)-2-nitroalk-1-enes on alumina surface without solvent. Synthesis 1985, 515-517.
-
(1985)
Synthesis
, pp. 515-517
-
-
Rosini, G.1
Ballini, R.2
Petrini, M.3
Sorrenti, P.4
-
13
-
-
0000226565
-
Nitration studies. XVIII. Conversion of lower nitroalkanes to higher members of the series
-
Bachman, G. B.; Maleski, R. J. Nitration studies. XVIII. conversion of lower nitroalkanes to higher members of the series. J. Org. Chem. 1972, 37, 2810-2814.
-
(1972)
J. Org. Chem.
, vol.37
, pp. 2810-2814
-
-
Bachman, G.B.1
Maleski, R.J.2
-
14
-
-
0010516738
-
Selective reduction of aromatic/aliphatic nitro groups by sodium sulfide
-
Huber, D.; Andermann, G.; Leclerc, G. Selective reduction of aromatic/aliphatic nitro groups by sodium sulfide. Tetrahedron Lett. 1988, 29, 635-638.
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 635-638
-
-
Huber, D.1
Andermann, G.2
Leclerc, G.3
-
15
-
-
0001078061
-
Non-Wittig type reaction of Tebbe reagent with acyl chloride
-
Chou, T. S.; Hung, S. B. Non-Wittig type reaction of Tebbe reagent with acyl chloride. Tetrahedron Lett. 1983, 24, 2169-2170.
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 2169-2170
-
-
Chou, T.S.1
Hung, S.B.2
-
16
-
-
0002695079
-
A new palladium catalyzed aromatic acetonylation by acetonyltributyltin
-
Kosugi, M.; Suzuki, M.; Hagiwara, I.; Goto, K.; Saitoh, K.; Migita, T. A new palladium catalyzed aromatic acetonylation by acetonyltributyltin. Chem. Lett. 1982, 939-940.
-
(1982)
Chem. Lett.
, pp. 939-940
-
-
Kosugi, M.1
Suzuki, M.2
Hagiwara, I.3
Goto, K.4
Saitoh, K.5
Migita, T.6
-
17
-
-
4243215300
-
β-3,4-methylenedioxyphenyl isopropyl amine
-
Elks, J.; Hey, D. H. β-3,4-Methylenedioxyphenyl isopropyl amine. J. Chem. Soc. 1943, 15-16.
-
(1943)
J. Chem. Soc.
, pp. 15-16
-
-
Elks, J.1
Hey, D.H.2
-
18
-
-
0022586217
-
A versatile synthesis of 1-aryl-2-nitro-3-(3,4,5-trimethoxyphenyl)- propenes as precursors of novel mescaline derivatives
-
Dauzonne, D.; Royer, R. A versatile synthesis of 1-aryl-2-nitro-3-(3,4,5- trimethoxyphenyl)-propenes as precursors of novel mescaline derivatives. Chem. Pharma. Bull. 1986, 34, 1628-1633.
-
(1986)
Chem. Pharma. Bull.
, vol.34
, pp. 1628-1633
-
-
Dauzonne, D.1
Royer, R.2
-
19
-
-
37049131587
-
Phenol oxidation and biosynthesis, Part XV: The biosynthesis of roemerine, anonaine and mecambrine
-
Barton, D. H. R.; Bhakuni, D. S.; Chapman, G. M.; Kirby, G. W. Phenol oxidation and biosynthesis, Part XV: the biosynthesis of roemerine, anonaine and mecambrine. J. Chem. Soc. C 1967, 2134-2140.
-
(1967)
J. Chem. Soc. C
, pp. 2134-2140
-
-
Barton, D.H.R.1
Bhakuni, D.S.2
Chapman, G.M.3
Kirby, G.W.4
-
20
-
-
0011189446
-
-
John Wiley & Sons; New York
-
Worrall, D. E.; Marvel, C. S.; Lycan, W. H. β-Nitrostyrene Organic Syntheses, Coll.; Vol. 1; 2nd ed. John Wiley & Sons; New York, 1956; pp. 413-415.
-
(1956)
β-Nitrostyrene Organic Syntheses, Coll.; Vol. 1; 2nd Ed.
, vol.1
, pp. 413-415
-
-
Worrall, D.E.1
Marvel, C.S.2
Lycan, W.H.3
-
21
-
-
33847090053
-
Nitro olefination of indoles and some substituted benzenes with 1-dimethylamino-2-nitroethylene
-
Buchi, G.; Mark, C.-P. Nitro olefination of indoles and some substituted benzenes with 1-dimethylamino-2-nitroethylene. J. Org. Chem. 1977, 42, 1784-1786.
-
(1977)
J. Org. Chem.
, vol.42
, pp. 1784-1786
-
-
Buchi, G.1
Mark, C.-P.2
-
22
-
-
0000485677
-
Nitroethylene: A stable, clean, and reactive agent for organic synthesis
-
Ranganathan, D.; Rao, C. B.; Ranganathan, S.; Mehrotra, A. K.; Iyengar, R. Nitroethylene: a stable, clean, and reactive agent for organic synthesis. J. Org. Chem. 1980, 45, 1185-1189.
-
(1980)
J. Org. Chem.
, vol.45
, pp. 1185-1189
-
-
Ranganathan, D.1
Rao, C.B.2
Ranganathan, S.3
Mehrotra, A.K.4
Iyengar, R.5
-
24
-
-
0006353536
-
The melting point and structure of tryptamine
-
Jackson, A. H.; Smith, A. E. The melting point and structure of tryptamine. J. Chem. Soc. 1965, 3498-3500.
-
(1965)
J. Chem. Soc.
, pp. 3498-3500
-
-
Jackson, A.H.1
Smith, A.E.2
-
25
-
-
84914348187
-
Configuration of stereoisomeric oximes and the structure of oxime N-ethers and aci-nitro derivatives
-
Auwers, K. V.; Ottens, B. Configuration of stereoisomeric oximes and the structure of oxime N-ethers and aci-nitro derivatives. Chem. Ber. 1924, 57B, 446-61.
-
(1924)
Chem. Ber.
, vol.57 B
, pp. 446-461
-
-
Auwers, K.V.1
Ottens, B.2
-
26
-
-
0012360477
-
p-Cyanophenol from p-nitrobenzaldoxime by an apparent dehydration-displacement, and a suggested modification of the Miller-Loudon conversion of aldehydes to nitriles
-
Knudsen, R. D.; Morrice, A. G.; Snyder, H. R. p-Cyanophenol from p-nitrobenzaldoxime by an apparent dehydration-displacement, and a suggested modification of the Miller-Loudon conversion of aldehydes to nitriles. J. Org. Chem. 1975, 40, 2878-2880.
-
(1975)
J. Org. Chem.
, vol.40
, pp. 2878-2880
-
-
Knudsen, R.D.1
Morrice, A.G.2
Snyder, H.R.3
-
27
-
-
2942698036
-
Beta-phenoxypropionic acid and some of its derivatives. Chromanone
-
Powell, S. G. Beta-phenoxypropionic acid and some of its derivatives. Chromanone. J. Am. Chem. Soc. 1923, 45, 2708-2711.
-
(1923)
J. Am. Chem. Soc.
, vol.45
, pp. 2708-2711
-
-
Powell, S.G.1
-
28
-
-
16444363402
-
Interpretation of the Hantzsch-Werner hypothesis
-
Forster, M. O.; Dunn, F. P. Interpretation of the Hantzsch-Werner hypothesis. J. Chem. Soc. 1909, 95, 425-433.
-
(1909)
J. Chem. Soc.
, vol.95
, pp. 425-433
-
-
Forster, M.O.1
Dunn, F.P.2
-
30
-
-
0003177688
-
Benzophenone oxime
-
Lachman, A. Benzophenone oxime. Org. Synth. 1930, 10, 10-11.
-
(1930)
Org. Synth.
, vol.10
, pp. 10-11
-
-
Lachman, A.1
-
31
-
-
0037119755
-
X = Y - ZH systems as potential 1,3-dipoles, Part 56: Cascade 1,3-azaprotio cyclotransfer-cycloaddition reactions between aldoximes and divinyl ketone: The effect of oxime E/Z isomerism on cycloaddition stereoselectivity
-
Blackwell, M.; Dunn, P. J.; Graham, A. B.; Grigg, R.; Higginson, P.; Saba, I. S.; Pett, T. M. X = Y - ZH systems as potential 1,3-dipoles, Part 56: Cascade 1,3-azaprotio cyclotransfer-cycloaddition reactions between aldoximes and divinyl ketone: the effect of oxime E/Z isomerism on cycloaddition stereoselectivity. Tetrahedron 2002, 58, 7715-7725.
-
(2002)
Tetrahedron
, vol.58
, pp. 7715-7725
-
-
Blackwell, M.1
Dunn, P.J.2
Graham, A.B.3
Grigg, R.4
Higginson, P.5
Saba, I.S.6
Pett, T.M.7
|