-
1
-
-
0001803662
-
Reduction of C=N to CHNH by metal hydrides
-
B. M. Trost and I. Fleming, Eds, Pergamon Press: Oxford
-
Hutchins, R. O.; Hutchins, M. K. Reduction of C=N to CHNH by metal hydrides. In Comprehensive Organic Synthesis; B. M. Trost and I. Fleming, (Eds.); Pergamon Press: Oxford, 1991; vol. 8; pp. 60-70.
-
(1991)
Comprehensive Organic Synthesis
, vol.8
, pp. 60-70
-
-
Hutchins, R.O.1
Hutchins, M.K.2
-
2
-
-
34547936934
-
Pd-C induced catalytic transfer hydrogenation with triethylsilane
-
(a) Mandal, P. K.; McMurry, J. S. Pd-C induced catalytic transfer hydrogenation with triethylsilane. J. Org. Chem. 2007,17, 6599-6601
-
(2007)
J. Org. Chem
, vol.17
, pp. 6599-6601
-
-
Mandal, P.K.1
McMurry, J.S.2
-
3
-
-
0032332565
-
Facile palladium- mediated conversion of ethanethiol esters to aldehydes and ketones
-
(b) Tokuyama, H.; Yokoshima, S.; Yamashita, T.; Lin, S.; Li, L.; Fukuyama, T. Facile palladium- mediated conversion of ethanethiol esters to aldehydes and ketones. J. Braz. Chem. Soc. 1998, 9, 381-387.
-
(1998)
J. Braz. Chem. Soc
, vol.9
, pp. 381-387
-
-
Tokuyama, H.1
Yokoshima, S.2
Yamashita, T.3
Lin, S.4
Li, L.5
Fukuyama, T.6
-
4
-
-
11644258796
-
Aminative reduction of ketones
-
Haskelberg, L. Aminative reduction of ketones. J. Am. Chem. Soc. 1948, 70, 2811-2812.
-
(1948)
J. Am. Chem. Soc
, vol.70
, pp. 2811-2812
-
-
Haskelberg, L.1
-
5
-
-
0348204126
-
A low-pressure reductive alkylation method for the conversion of ketones to primary amines
-
Alexander, E. R.; Misegades, A. L. A low-pressure reductive alkylation method for the conversion of ketones to primary amines. J. Am. Chem. Soc. 1948, 70, 1315-1316.
-
(1948)
J. Am. Chem. Soc
, vol.70
, pp. 1315-1316
-
-
Alexander, E.R.1
Misegades, A.L.2
-
6
-
-
0142174037
-
Reduction of Schiff bases with isopropyl alcohol and aluminium isopropoxide in the presence of Raney nickel
-
Botta, M.; Angelis, F. D.; Gambacorta, A.; Labbiento, L.; Nicoletti, R. Reduction of Schiff bases with isopropyl alcohol and aluminium isopropoxide in the presence of Raney nickel. J. Org. Chem. 1985, 50, 1916-1919.
-
(1985)
J. Org. Chem
, vol.50
, pp. 1916-1919
-
-
Botta, M.1
Angelis, F.D.2
Gambacorta, A.3
Labbiento, L.4
Nicoletti, R.5
-
7
-
-
67650238692
-
Reductive amination of ketones
-
U.S. Pat. No. 3,187,047, 9873f
-
Green, M. Reductive amination of ketones. U.S. Pat. No. 3,187,047, 1965; Chem. Abstr. 1965, 53, 9873f.
-
(1965)
Chem. Abstr
, vol.53
-
-
Green, M.1
-
8
-
-
0030047724
-
Simple NaBH4 in presence of transition metal compounds
-
Demir, A. S.; Tanycli, C.; Sesenoglu, O.; Demic, S. A. Simple NaBH4 in presence of transition metal compounds. Tetrahedron Lett. 1996, 37, 407-410.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 407-410
-
-
Demir, A.S.1
Tanycli, C.2
Sesenoglu, O.3
Demic, S.A.4
-
9
-
-
0001145989
-
Synthese d'aziridines secondaries disubstituees.
-
Diab, Y.; Laurent, A.; Mison, P. Synthese d'aziridines secondaries disubstituees. Tetrahedron Lett. 1974, 15, 1605-1607.
-
(1974)
Tetrahedron Lett
, vol.15
, pp. 1605-1607
-
-
Diab, Y.1
Laurent, A.2
Mison, P.3
-
10
-
-
33748869055
-
Catalytic transfer hydrogenastion of imines to secondary amines using inexpensive commercial zinc dust and ammonim formate
-
Abiraj, K.; Dinesh, B.; Srinivasa, G. R.; Channe Gowda, D. Catalytic transfer hydrogenastion of imines to secondary amines using inexpensive commercial zinc dust and ammonim formate. J. Chem. Res. 2006, 8, 534-535.
-
(2006)
J. Chem. Res
, vol.8
, pp. 534-535
-
-
Abiraj, K.1
Dinesh, B.2
Srinivasa, G.R.3
Channe Gowda, D.4
-
12
-
-
0037237179
-
A simple protocol for direct reductive amination of aldehydes and ketones using potassium formate and catalytic palladium acetate
-
Basudeb, B.; Jha, S.; Bhuiyan, M. M. H.; Das, P. A simple protocol for direct reductive amination of aldehydes and ketones using potassium formate and catalytic palladium acetate. Synlett. 2003, 4, 555-557.
-
(2003)
Synlett
, vol.4
, pp. 555-557
-
-
Basudeb, B.1
Jha, S.2
Bhuiyan, M.M.H.3
Das, P.4
-
13
-
-
0032482298
-
Sodium borohydride on wet clay: Solvent-free reductive amination of carbonyl compounds using microwaves
-
Varma, R. S.; Dahiya, R. Sodium borohydride on wet clay: Solvent-free reductive amination of carbonyl compounds using microwaves. Tetrahedron 1998, 54, 6293-6298.
-
(1998)
Tetrahedron
, vol.54
, pp. 6293-6298
-
-
Varma, R.S.1
Dahiya, R.2
-
14
-
-
0010913027
-
Reduction of oximes with hydrosilane/H+ reagent
-
Fujita, M.; Oishi, H.; Hiyama, T. Reduction of oximes with hydrosilane/H+ reagent. Chem. Lett. 1986, 837-838.
-
(1986)
Chem. Lett
, pp. 837-838
-
-
Fujita, M.1
Oishi, H.2
Hiyama, T.3
-
17
-
-
0035847482
-
Novel triethylsilane mediated reductive N-alkylation of amines: Improved synthesis of 1-(4-imidazolyl)methyl-4-sulfonyl benzodiazepines, new farnesyltransferase inhibitors
-
Chen, B. C.; Sundeen, J. E.; Guo, P.; Bednarz, M. S.; Zhao, R. Novel triethylsilane mediated reductive N-alkylation of amines: Improved synthesis of 1-(4-imidazolyl)methyl-4-sulfonyl benzodiazepines, new farnesyltransferase inhibitors. Tetrahedron Lett. 2001, 42, 1245-1246.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 1245-1246
-
-
Chen, B.C.1
Sundeen, J.E.2
Guo, P.3
Bednarz, M.S.4
Zhao, R.5
-
18
-
-
84987123520
-
The Barbier reaction-A one-step alternative for syntheses via organomagnissum compounds
-
(a) Blomberg, C.; Hartog, F. A. The Barbier reaction-A one-step alternative for syntheses via organomagnissum compounds. Synthesis. 1977, 1, 18-30
-
(1977)
Synthesis
, vol.1
, pp. 18-30
-
-
Blomberg, C.1
Hartog, F.A.2
-
19
-
-
0344444621
-
Magnesium/ammonium formate promoted rapid, low cost, and selective reduction of nitro compounds
-
(b) Srinivasa, G. R.; Abiraj, K.; Channe Gowda, D. Magnesium/ammonium formate promoted rapid, low cost, and selective reduction of nitro compounds. Indian J. Chem. 2003, 42B, 2882-2884
-
(2003)
Indian J. Chem
, vol.42 B
, pp. 2882-2884
-
-
Srinivasa, G.R.1
Abiraj, K.2
Channe Gowda, D.3
-
20
-
-
1542530948
-
Magnesium-catalyzed proficient reduction of oximes to amines using ammonium formate
-
(c) Abiraj, K.; Channe Gowda, D. Magnesium-catalyzed proficient reduction of oximes to amines using ammonium formate. Synth. Commun. 2004, 34, 599-605.
-
(2004)
Synth. Commun
, vol.34
, pp. 599-605
-
-
Abiraj, K.1
Channe Gowda, D.2
-
21
-
-
0032542198
-
Indium promoted reductive homocoupling of alkyl and aryl halides
-
(a) Ranu, B. C.; Dutta, P.; Sarkar, A. Indium promoted reductive homocoupling of alkyl and aryl halides. Tetrahedron Lett. 1998, 39, 9557-9558
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 9557-9558
-
-
Ranu, B.C.1
Dutta, P.2
Sarkar, A.3
-
22
-
-
0033806181
-
Indium/ammonium chloride mediated selective reduction of aromatic nitro compounds: Practical synthesis of 6-aminochrysene
-
(b) Banik, B. K.; Suhendra, M.; Banik, I.; Becker, F. F. Indium/ammonium chloride mediated selective reduction of aromatic nitro compounds: Practical synthesis of 6-aminochrysene. Synth. Commun. 2000, 30, 3745-3754.
-
(2000)
Synth. Commun
, vol.30
, pp. 3745-3754
-
-
Banik, B.K.1
Suhendra, M.2
Banik, I.3
Becker, F.F.4
-
23
-
-
0001695687
-
Preparation of new classes of aliphatic, allylic, and benzylic zinc and copper reagents by the insertion of zinc dust into organic halides, phosphates, and sulfonates
-
Jubert, C.; Knochel, P. Preparation of new classes of aliphatic, allylic, and benzylic zinc and copper reagents by the insertion of zinc dust into organic halides, phosphates, and sulfonates. J. Org. Chem. 1992, 57, 5425-5431.
-
(1992)
J. Org. Chem
, vol.57
, pp. 5425-5431
-
-
Jubert, C.1
Knochel, P.2
-
24
-
-
37049078348
-
Tin-promoted stereocontrolled intramolecular allylation of carbonyl compounds: A facile and stereoselective method for ring construction
-
Zhou, J. Y.; Chen, Z. G.; Wu, S. H. Tin-promoted stereocontrolled intramolecular allylation of carbonyl compounds: A facile and stereoselective method for ring construction. Chem. Commun. 1994, 24, 2783-2784.
-
(1994)
Chem. Commun
, vol.24
, pp. 2783-2784
-
-
Zhou, J.Y.1
Chen, Z.G.2
Wu, S.H.3
-
25
-
-
0030070673
-
A convenient synthesis of p,y-unsaturated ketones through zinc mediated allylation of acid chlorides
-
Ranu, B. C.; Majee, A.; Das, A. R. A convenient synthesis of p,y-unsaturated ketones through zinc mediated allylation of acid chlorides. Tetrahedron Lett. 1996, 37, 1109-1112.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 1109-1112
-
-
Ranu, B.C.1
Majee, A.2
Das, A.R.3
-
26
-
-
85047674782
-
Facile and efficient synthesis of homo- allylic alcohols using allyl bromide and commercial zinc dust
-
Ranu, B. C.; Majee, A.; Das, A. R. Facile and efficient synthesis of homo- allylic alcohols using allyl bromide and commercial zinc dust. Tetrahedron Lett. 1995, 36, 4885-4888.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 4885-4888
-
-
Ranu, B.C.1
Majee, A.2
Das, A.R.3
-
27
-
-
0032482531
-
Zinc mediated facile amide formation: Application to alkyl, aryl, heterocycle, carbohydrate, and amino acids
-
Meshram, H. M.; Reddy, G. S.; Reddy, M. M.; Yadav, J. S. Zinc mediated facile amide formation: Application to alkyl, aryl, heterocycle, carbohydrate, and amino acids. Tetrahedron Lett. 1998, 39, 4103-4106.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4103-4106
-
-
Meshram, H.M.1
Reddy, G.S.2
Reddy, M.M.3
Yadav, J.S.4
-
28
-
-
0032516323
-
Zinc promoted simple and convenient synthesis of carbamates: An easy access for amino group protection
-
and references cited there in
-
Yadav, J. S.; Reddy, G. S.; Reddy, M. M.; Meshram, H. M. Zinc promoted simple and convenient synthesis of carbamates: An easy access for amino group protection. Tetrahedron Lett. 1998, 39, 3259-3262, and references cited there in.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 3259-3262
-
-
Yadav, J.S.1
Reddy, G.S.2
Reddy, M.M.3
Meshram, H.M.4
-
29
-
-
0035043794
-
-
Mahesh, B.; Shankare Gowda; Channe Gowda, D. Zinc catalyzed ammonium formate reductions: Rapid and selective reduction of aliphatic and aromatic nitro compounds. Indian J. Chem. 2001, 40B, 75-77
-
(a) Mahesh, B.; Shankare Gowda; Channe Gowda, D. Zinc catalyzed ammonium formate reductions: Rapid and selective reduction of aliphatic and aromatic nitro compounds. Indian J. Chem. 2001, 40B, 75-77
-
-
-
-
30
-
-
0037231736
-
-
Shankare, Gowda; Channe Gowda, D. Zinc/hydrazine: A low-cost, facile system for the reductions of nitro compounds. Indian J. Chem. 2003, 42B, 180-183
-
(b) Shankare, Gowda; Channe Gowda, D. Zinc/hydrazine: A low-cost, facile system for the reductions of nitro compounds. Indian J. Chem. 2003, 42B, 180-183
-
-
-
-
31
-
-
33645340595
-
Polymer- supported formate and zinc: A novel system for the transfer hydrogenation of aromatic nitro compounds
-
(c) Srinivasa, G. R.; Abiraj, K.; Channe Gowda, D. Polymer- supported formate and zinc: A novel system for the transfer hydrogenation of aromatic nitro compounds. Indian J. Chem. 2006, 45B, 297-301.
-
(2006)
Indian J. Chem
, vol.45 B
, pp. 297-301
-
-
Srinivasa, G.R.1
Abiraj, K.2
Channe Gowda, D.3
-
32
-
-
26844549548
-
Reduction of olefins using ruthenium carbene catalysts and silanes
-
Menozzi, C.; Dalko, P. I.; Cossy, J. Reduction of olefins using ruthenium carbene catalysts and silanes. Synlett. 2005, 16, 2449-2452.
-
(2005)
Synlett
, vol.16
, pp. 2449-2452
-
-
Menozzi, C.1
Dalko, P.I.2
Cossy, J.3
-
33
-
-
0000802385
-
PdCl2-catalyzed reduction of organic halides by triethylsilane
-
Boukherroub, R.; Chatgilialoglu, C.; Manuel, G. PdCl2-catalyzed reduction of organic halides by triethylsilane. Organometallics 1996, 15, 1508-1510.
-
(1996)
Organometallics
, vol.15
, pp. 1508-1510
-
-
Boukherroub, R.1
Chatgilialoglu, C.2
Manuel, G.3
-
34
-
-
33748523800
-
N-2(Nitrobenzylidene)aniline
-
Sec E62
-
Naveen, S.; Anil Kumar, K.; Channe Gowda, D.; Sridhar, M. A.; Shashidhara Prasad, J. N-2(Nitrobenzylidene)aniline. Acta Crystallographica 2006, Sec E62, 3790-3791.
-
(2006)
Acta Crystallographica
, pp. 3790-3791
-
-
Naveen, S.1
Anil Kumar, K.2
Channe Gowda, D.3
Sridhar, M.A.4
Shashidhara Prasad, J.5
-
35
-
-
67650262771
-
-
Vogel, A. I. Text Book of Practical Organic Chemistry, 5th ed.; revised by B. S. Furniss, A. J. Hannaford, P. W. G. Smith, and A. R. Tatchell (Eds.); Addison Wesley Longman Limited: Essex, UK. 1997; p. 1298.
-
Vogel, A. I. Text Book of Practical Organic Chemistry, 5th ed.; revised by B. S. Furniss, A. J. Hannaford, P. W. G. Smith, and A. R. Tatchell (Eds.); Addison Wesley Longman Limited: Essex, UK. 1997; p. 1298.
-
-
-
-
36
-
-
0000638698
-
Reduction of Schiff bases with sodium borohydride
-
Billman, J. H.; Diesing, A. C. Reduction of Schiff bases with sodium borohydride. J. Org. Chem. 1957, 22, 1068-1070.
-
(1957)
J. Org. Chem
, vol.22
, pp. 1068-1070
-
-
Billman, J.H.1
Diesing, A.C.2
-
37
-
-
84993866919
-
The photochemical reactions of the halogenated N-benzylanilines mechanism of the reactions
-
Park, Y. T.; Lee, I. H.; Kim, Y. H. The photochemical reactions of the halogenated N-benzylanilines mechanism of the reactions. J. Heterocycl. Chem. 1994, 31, 1625-1629.
-
(1994)
J. Heterocycl. Chem
, vol.31
, pp. 1625-1629
-
-
Park, Y.T.1
Lee, I.H.2
Kim, Y.H.3
-
38
-
-
0008349006
-
Mechanism of amination with soda- mide: New procedure for the preparation of substituted amindines
-
Kirsunov, A. V.; Ivashchenko, Y. N. Mechanism of amination with soda- mide: New procedure for the preparation of substituted amindines. Chem. Abstr. 1953, 30, 1775-1777.
-
(1953)
Chem. Abstr
, vol.30
, pp. 1775-1777
-
-
Kirsunov, A.V.1
Ivashchenko, Y.N.2
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