-
1
-
-
0001311980
-
-
D. Barton, D. W. Ollis, I. O. Sutherland (Eds.)Pergamon Press: Oxford
-
Tennant, G. In Comprehensive Organic Chemistry; D. Barton, D. W. Ollis, I. O. Sutherland (Eds.); Pergamon Press: Oxford, 1979; vol. 2, p. 528.
-
(1979)
Comprehensive Organic Chemistry
, vol.2
, pp. 528
-
-
Tennant, G.1
-
2
-
-
0035121806
-
A one-pot method for the efficient preparation of aromatic nitriles from aldehydes using ammonia magnesium sulfate and manganese dioxide
-
Lai G.,Bhamare N. K.,Anderson W. K., A one-pot method for the efficient preparation of aromatic nitriles from aldehydes using ammonia magnesium sulfate and manganese dioxide, Synlett, 2001, 230-231.
-
(2001)
Synlett
, pp. 230-231
-
-
Lai, G.1
Bhamare, N.K.2
Anderson, W.K.3
-
3
-
-
0032546525
-
2-symmetry-based design of bis-sulfonamide dihydropyrones
-
2-symmetry-based design of bis-sulfonamide dihydropyrones. Bioorg. Med. Chem. Lett. 1998, 8, 1237-1242.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1237-1242
-
-
Janakiraman, M.N.1
Watenpaugh, K.D.2
Tomich, P.K.3
Chong, K.T.4
Turner, S.R.5
Tommasi, R.A.6
Thaisrivongs, S.7
Strohbach, J.W.8
-
4
-
-
0033593962
-
Syntheses and biological activities of bis(3-indo-lyl)thiazoles, analogues of marine bis(indole)alkaloid nortopsentins
-
Gu, X.-H.; Wan, X.-Z.; Jiang, B. Syntheses and biological activities of bis(3-indo-lyl)thiazoles, analogues of marine bis(indole)alkaloid nortopsentins. Bioorg. Med. Chem. Lett. 1999, 9, 569-572
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 569-572
-
-
Gu, X.-H.1
Wan, X.-Z.2
Jiang, B.3
-
5
-
-
0029067662
-
Novel thiazole derivatives as inhibitors of superoxide production by human neutrophils: Synthesis and structure-activity relationships
-
Chihiro, M.; Nagamoto, H.; Tekemura, I.; Kitano, K.; Komatsu, H.; Sekiguchi, K.; Tabusa, F.; Mori, T.; Tominaga, M.; Yabuuchi, Y. Novel thiazole derivatives as inhibitors of superoxide production by human neutrophils: Synthesis and structure-activity relationships. J. Med. Chem. 1995, 38, 353-358.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 353-358
-
-
Chihiro, M.1
Nagamoto, H.2
Tekemura, I.3
Kitano, K.4
Komatsu, H.5
Sekiguchi, K.6
Tabusa, F.7
Mori, T.8
Tominaga, M.9
Yabuuchi, Y.10
-
6
-
-
0032576816
-
Natural kaolinitic clay-catalyzed conversion of nitriles to 2-oxazolines
-
Jnaneshwara, G. K.; Deshpande, V. H.; Lalithambika, M.; Ravindranathan, T.; Bedekar, A. V. Natural kaolinitic clay-catalyzed conversion of nitriles to 2-oxazolines. Tetrahedron Lett. 1998, 39 (5-6), 459-462.
-
(1998)
Tetrahedron Lett.
, vol.39
, Issue.5-6
, pp. 459-462
-
-
Jnaneshwara, G.K.1
Deshpande, V.H.2
Lalithambika, M.3
Ravindranathan, T.4
Bedekar, A.V.5
-
7
-
-
33751384910
-
Dialkyltin oxide-mediated addition of trimethylsilyl azide to nitriles: A novel preparation of 5-substituted tetrazols
-
Wittenberger, S. J.; Donner, B. G. Dialkyltin oxide-mediated addition of trimethylsilyl azide to nitriles: A novel preparation of 5-substituted tetrazols. J. Org. Chem. 1993, 58, 4139-4141
-
(1993)
J. Org. Chem.
, vol.58
, pp. 4139-4141
-
-
Wittenberger, S.J.1
Donner, B.G.2
-
8
-
-
0027081168
-
Antirhinoviral activity of heterocyclic analogs of Win 54954
-
Bailey, T. R.; Diana, G. D.; Kowalczyk, P. J.; Akullian, V.; Eissenstat, M. A.; Cutcliffe, D.; Mallamo, J. P.; Carabateas, P.; Pevear, D. C. Antirhinoviral activity of heterocyclic analogs of Win 54954. J. Med. Chem. 1992, 35, 4628-4633
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4628-4633
-
-
Bailey, T.R.1
Diana, G.D.2
Kowalczyk, P.J.3
Akullian, V.4
Eissenstat, M.A.5
Cutcliffe, D.6
Mallamo, J.P.7
Carabateas, P.8
Pevear, D.C.9
-
9
-
-
85034956876
-
Role of protic and dipolar aprotic solvents in heterocyclic syntheses via 1,3-dipolar cycloaddition reactions
-
Kadaba, P. K. Role of protic and dipolar aprotic solvents in heterocyclic syntheses via 1,3-dipolar cycloaddition reactions. Synthesis 1973, 6, 71-84.
-
(1973)
Synthesis
, vol.6
, pp. 71-84
-
-
Kadaba, P.K.1
-
10
-
-
0042677746
-
Chapter 1: The synthesis of oxazoles from diazocarbonyl compounds
-
Moody, C. J.; Doyle, K. J. Chapter 1: The synthesis of oxazoles from diazocarbonyl compounds. Prog. Heterocyclic Chem., 1997 9, 1-16.
-
(1997)
Prog. Heterocyclic Chem.
, vol.9
, pp. 1-16
-
-
Moody, C.J.1
Doyle, K.J.2
-
11
-
-
0034072954
-
Synthesis and reactivity of 4-silylated oxazoles
-
Ducept, P. C.; Marsden, S. P. Synthesis and reactivity of 4-silylated oxazoles. Synlett 2000, 5, 692-694.
-
(2000)
Synlett
, vol.5
, pp. 692-694
-
-
Ducept, P.C.1
Marsden, S.P.2
-
12
-
-
0033042179
-
Angiotensin receptor subtypes: Novel targets for cardiovascular therapy
-
Fabiani, M. E. Angiotensin receptor subtypes: Novel targets for cardiovascular therapy. Drug News Perspect. 1999, 12, 207-215.
-
(1999)
Drug News Perspect.
, vol.12
, pp. 207-215
-
-
Fabiani, M.E.1
-
14
-
-
0035742524
-
Catalysis for green chemistry
-
Clark, J. H. Catalysis for green chemistry. Pure Appl. Chem. 2001, 73, 103-111.
-
(2001)
Pure Appl. Chem.
, vol.73
, pp. 103-111
-
-
Clark, J.H.1
-
15
-
-
33947463198
-
The preparation of nitriles
-
Mowry, D. T. The preparation of nitriles. Chem. Rev. 1948, 42, 189-283.
-
(1948)
Chem. Rev.
, vol.42
, pp. 189-283
-
-
Mowry, D.T.1
-
16
-
-
0000827879
-
Nitroxyl-mediated electro-oxidation of amines to nitriles and carbonyl compounds
-
Semmelhack, M. F.; Schmid, C. R. Nitroxyl-mediated electro-oxidation of amines to nitriles and carbonyl compounds. J. Am. Chem. Soc. 1983, 105, 6732-6734
-
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 6732-6734
-
-
Semmelhack, M.F.1
Schmid, C.R.2
-
17
-
-
0346753440
-
Selective and mild oxidation of primary amines to nitriles with trichloroisocyanuric acid
-
Chen, F. E.; Kuang, Y. Y.; Dai, H. F.; Lu, L.; Huo, M. A. Selective and mild oxidation of primary amines to nitriles with trichloroisocyanuric acid. Synthesis 2003, 17, 2629-2631.
-
(2003)
Synthesis
, vol.17
, pp. 2629-2631
-
-
Chen, F.E.1
Kuang, Y.Y.2
Dai, H.F.3
Lu, L.4
Huo, M.A.5
-
18
-
-
0036250776
-
A clean conversion of aldehydes to nitriles using a solid-supported hydrazine
-
Baxendale, I. R.; Ley, S. V.; Sneddon, F. H. A clean conversion of aldehydes to nitriles using a solid-supported hydrazine. Synlett 2002, 5, 775-777
-
(2002)
Synlett
, vol.5
, pp. 775-777
-
-
Baxendale, I.R.1
Ley, S.V.2
Sneddon, F.H.3
-
19
-
-
33846005816
-
A convenient new procedure for converting primary amides into nitriles
-
Kuo, C. W.; Zhu, J. L.; Wu, J. D.; Chu, C. M.; Yao, C. F.; Shia, K. S. A convenient new procedure for converting primary amides into nitriles. Chem. Commun. 2007, 301-303
-
(2007)
Chem. Commun.
, pp. 301-303
-
-
Kuo, C.W.1
Zhu, J.L.2
Wu, J.D.3
Chu, C.M.4
Yao, C.F.5
Shia, K.S.6
-
20
-
-
0010785608
-
Mechanism of the von Braun amide degradations with carbonyl bromide or phosphorus penta bromide
-
Phillips, B. A.; Fodor, G.; Gal, J.; Letourneau, F.; Ryan, J. J. Mechanism of the von Braun amide degradations with carbonyl bromide or phosphorus penta bromide. Tetrahedron 1973, 29, 3309-3327.
-
(1973)
Tetrahedron
, vol.29
, pp. 3309-3327
-
-
Phillips, B.A.1
Fodor, G.2
Gal, J.3
Letourneau, F.4
Ryan, J.J.5
-
21
-
-
36849020947
-
A novel and efficient synthesis of nitriles from aldehydes under solvent-free microwave irradiation conditions
-
Lee, J. C.; Yoon, J. M.; Baek, J. W. A novel and efficient synthesis of nitriles from aldehydes under solvent-free microwave irradiation conditions. Bull. Korean Chem. Soc. 2007, 28, 29-30.
-
(2007)
Bull. Korean Chem. Soc.
, vol.28
, pp. 29-30
-
-
Lee, J.C.1
Yoon, J.M.2
Baek, J.W.3
-
22
-
-
0035808924
-
Direct transformation of aldehydes to nitriles using iodine in ammonia water
-
Talukdar, S.; Hsu, J.; Chou, T.; Fang, J. Direct transformation of aldehydes to nitriles using iodine in ammonia water. Tetrahedran Lett. 2001, 42, 1103.
-
(2001)
Tetrahedran Lett.
, vol.42
, pp. 1103
-
-
Talukdar, S.1
Hsu, J.2
Chou, T.3
Fang, J.4
-
23
-
-
0026751668
-
A convenient one-step method of converting electron-rich aromatic aldehydes into nitriles
-
Suzuki, H.; Nakaya, C. A convenient one-step method of converting electron-rich aromatic aldehydes into nitriles. synthesis 1992, 7, 641-642.
-
(1992)
Synthesis
, vol.7
, pp. 641-642
-
-
Suzuki, H.1
Nakaya, C.2
-
24
-
-
33846976120
-
2
-
2. Synth. Commun. 2007, 37, 257-259.
-
(2007)
Synth. Commun.
, vol.37
, pp. 257-259
-
-
Digambar, D.G.1
Sameer, V.R.2
Babasaheb, V.K.3
Shisodia, S.U.4
Ravikumar, M.B.5
Praveen, S.S.6
Sunil, S.C.7
Rajendra, P.P.8
-
25
-
-
67651092214
-
0-disubstituted ureas=thioureas by a zinc chloride-catalyzed thermal reaction
-
0-disubstituted ureas=thioureas by a zinc chloride-catalyzed thermal reaction. Synth. Commun. 2009, 39, 2928-2934
-
(2009)
Synth. Commun.
, vol.39
, pp. 2928-2934
-
-
Pasha, M.A.1
Madhusudana Reddy, M.B.2
-
26
-
-
33846240529
-
Molecular iodine-catalyzed synthesis of aryl-14H-dibenzo[a,j]xanthenes under solvent-free condition
-
Pasha, M. A.; Jayashankara, V. P. Molecular iodine-catalyzed synthesis of aryl-14H-dibenzo[a,j]xanthenes under solvent-free condition. Bioorg. Med. Chem. Lett. 2007, 17, 621-623
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 621-623
-
-
Pasha, M.A.1
Jayashankara, V.P.2
-
27
-
-
34248587905
-
A simple and efficient procedure for the one-pot synthesis of b-acetamido-b-aryl-propiophenones by molecular iodine catalyzed tandem reaction
-
Pasha, M. A.; Jayashankara, V. P.; Swamy, N. R. A simple and efficient procedure for the one-pot synthesis of b-acetamido-b-aryl-propiophenones by molecular iodine catalyzed tandem reaction. Synth. Commun. 2007, 37, 1551-1556
-
(2007)
Synth. Commun.
, vol.37
, pp. 1551-1556
-
-
Pasha, M.A.1
Jayashankara, V.P.2
Swamy, N.R.3
-
28
-
-
34248589189
-
2 using microwaves under different reaction conditions
-
2 using microwaves under different reaction conditions. Synth. Commun. 2007, 37, 1545-1550
-
(2007)
Synth. Commun.
, vol.37
, pp. 1545-1550
-
-
Manjula, K.1
Pasha, M.A.2
-
29
-
-
77951026580
-
2-catalysed expeditious route to nitriles
-
2-catalysed expeditious route to nitriles. Synth. Commun. 2010, 40, 1276-1279.
-
(2010)
Synth. Commun.
, vol.40
, pp. 1276-1279
-
-
Pasha, M.A.1
Nizam, A.2
-
30
-
-
62649143644
-
Microwave-enhanced synthesis
-
Caddick, S.; Fitzmaurice, R. Microwave-enhanced synthesis. Tetrahedron 2009, 65(17), 3325-3355.
-
(2009)
Tetrahedron
, vol.65
, Issue.17
, pp. 3325-3355
-
-
Caddick, S.1
Fitzmaurice, R.2
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