-
2
-
-
33845282176
-
Hapalindoles, antibacterial and antimycotic alkaloids from the cyanophyte Hapalosiphon fontinalis
-
(a) Moore, R. E.; Cheuk, C.; Yang, X. Q.; Patterson, G. M. I.; Bonjouklian, R.; Smika, T. A.; Mynderse, J.; Foster, R. S.; Jones, N. D.; Skiartzendruber, J. K.; Deeter, J. B. Hapalindoles, antibacterial and antimycotic alkaloids from the cyanophyte Hapalosiphon fontinalis. J. Org. Chem. 1987, 52, 1036;
-
(1987)
J. Org. Chem
, vol.52
, pp. 1036
-
-
Moore, R.E.1
Cheuk, C.2
Yang, X.Q.3
Patterson, G.M.I.4
Bonjouklian, R.5
Smika, T.A.6
Mynderse, J.7
Foster, R.S.8
Jones, N.D.9
Skiartzendruber, J.K.10
Deeter, J.B.11
-
3
-
-
0000285258
-
Addition and annulation reactions between indoles and α,β-unsaturated ketones
-
(b) Garnick, R. L.; Levery, S. B.; LeQuesne, U. P. Addition and annulation reactions between indoles and α,β-unsaturated ketones. J. Org. Chem. 1978, 43, 1226.
-
(1978)
J. Org. Chem
, vol.43
, pp. 1226
-
-
Garnick, R.L.1
Levery, S.B.2
LeQuesne, U.P.3
-
4
-
-
37049076280
-
Control of asymmetry through conjugate addition reactions
-
(a) Leonard, J. Control of asymmetry through conjugate addition reactions. Contemp. Org. Synth. 1994, 1, 387;
-
(1994)
Contemp. Org. Synth
, vol.1
, pp. 387
-
-
Leonard, J.1
-
5
-
-
0001040147
-
Asymmetric conjugate addition
-
(b) Rossiter, B. E.; Swingle, N. M. Asymmetric conjugate addition. Chem. Rev. 1992, 92, 771.
-
(1992)
Chem. Rev
, vol.92
, pp. 771
-
-
Rossiter, B.E.1
Swingle, N.M.2
-
6
-
-
0003527998
-
The nitro group of organic synthesis
-
Wiley-VCH: New York
-
(a) Ono, N. The nitro group of organic synthesis. In The Nitro Group of Organic Synthesis; Wiley-VCH: New York, 2001;
-
(2001)
The Nitro Group of Organic Synthesis
-
-
Ono, N.1
-
7
-
-
0002831079
-
Nitroaliphatic compounds- ideal intermediates in organic synthesis
-
(b) Seebach, D.; Colvin, E. W.; Lehr, F.; Weller, T. Nitroaliphatic compounds- ideal intermediates in organic synthesis. Chimia 1979, 33, 1;
-
(1979)
Chimia
, vol.33
, pp. 1
-
-
Seebach, D.1
Colvin, E.W.2
Lehr, F.3
Weller, T.4
-
8
-
-
84985606357
-
-
Calderari, G.; Seebach, D. Asymmetrische Michael-additionen. Stereoselektive alkylierung chiraler, nicht racemischer enolate durch nitroolefine. Herstellung enantiomerenrein γ-aminobuttersäure- und bernsteinsäure-derivate. Helv. Chim. Acta 1985, 68, 1592.
-
(c) Calderari, G.; Seebach, D. Asymmetrische Michael-additionen. Stereoselektive alkylierung chiraler, nicht racemischer enolate durch nitroolefine. Herstellung enantiomerenrein γ-aminobuttersäure- und bernsteinsäure-derivate. Helv. Chim. Acta 1985, 68, 1592.
-
-
-
-
11
-
-
0042233997
-
Enantioselective indole Friedel-Crafts alkylations catalyzed by bis(oxazolinyl) pyridine-scandium(III) triflate complexes
-
(b) Evans, D. A.; Scheidt, K. A.; Fandrick, K. R.; Lann, H. W.; Wu, J. Enantioselective indole Friedel-Crafts alkylations catalyzed by bis(oxazolinyl) pyridine-scandium(III) triflate complexes. J. Am. Chem. Soc. 2003, 125, 10780;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 10780
-
-
Evans, D.A.1
Scheidt, K.A.2
Fandrick, K.R.3
Lann, H.W.4
Wu, J.5
-
12
-
-
0037969443
-
Catalytic enantioselective conjugate addition of indoles to simple α,β-unsaturated ketones
-
(c) Bandini, M.; Fagioli, M.; Melchiorre, P.; Melloni, A.; Umani-Ronchi, A. Catalytic enantioselective conjugate addition of indoles to simple α,β-unsaturated ketones. Tetrahedron Lett. 2003, 44, 5843;
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 5843
-
-
Bandini, M.1
Fagioli, M.2
Melchiorre, P.3
Melloni, A.4
Umani-Ronchi, A.5
-
13
-
-
0037205013
-
3-catalyzed 1,4- then 1,2-nucleophilic addition to enones
-
3-catalyzed 1,4- then 1,2-nucleophilic addition to enones. J. Org. Chem. 2002, 67, 3700.
-
(2002)
J. Org. Chem
, vol.67
, pp. 3700
-
-
Bandini, M.1
Cozzi, P.G.2
Giacomini, M.3
Melchiorre, P.4
Selva, S.5
Umani-Ronchi, A.6
-
14
-
-
0142060629
-
Silica sulfuric acid: An efficient catalyst for the direct conversion of primary and secondary trimethylsilyl ethers to their corresponding ethers under mild and heterogeneous conditions
-
(a) Zolfigol, M. A.; Mohammadpoor-Baltork, I.; Mirjalil, B. F.; Bamoniri, A. Silica sulfuric acid: an efficient catalyst for the direct conversion of primary and secondary trimethylsilyl ethers to their corresponding ethers under mild and heterogeneous conditions. Synlett 2003, 1877;
-
(2003)
Synlett
, pp. 1877
-
-
Zolfigol, M.A.1
Mohammadpoor-Baltork, I.2
Mirjalil, B.F.3
Bamoniri, A.4
-
15
-
-
0037474675
-
Silica sulfuric acid: An efficient and reusable catalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones
-
(b) Salehi, P.; Dabiri, M.; Zolfigol, M. A.; Bodaghi Fard, M. A. Silica sulfuric acid: an efficient and reusable catalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones. Tetrahedron Lett. 2003, 44, 2889;
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 2889
-
-
Salehi, P.1
Dabiri, M.2
Zolfigol, M.A.3
Bodaghi Fard, M.A.4
-
16
-
-
18744388642
-
-
Salehi, P.; Dabiri, M.; Zolfigol, M. A.; Boghban Zadeh, M. Novel method for the one-pot three-component synthesis of 2,3-dihydroquinazolin- 4(1h)-ones. Synlett 2005, 1155;
-
(c) Salehi, P.; Dabiri, M.; Zolfigol, M. A.; Boghban Zadeh, M. Novel method for the one-pot three-component synthesis of 2,3-dihydroquinazolin- 4(1h)-ones. Synlett 2005, 1155;
-
-
-
-
17
-
-
0036400031
-
2 as a novel heterogeneous system for the chemoselective N-nitrosation of secondary amines under mild conditions
-
2 as a novel heterogeneous system for the chemoselective N-nitrosation of secondary amines under mild conditions. Synlett 2002, 1621;
-
(2002)
Synlett
, pp. 1621
-
-
Zolfigol, M.A.1
Abdolhamid, B.2
-
18
-
-
0036920273
-
2 as a novel heterogeneous system for the oxidation of 1,4-dihydropyridines under mild conditions
-
2 as a novel heterogeneous system for the oxidation of 1,4-dihydropyridines under mild conditions. Green. Chem. 2002, 4, 562;
-
(2002)
Green. Chem
, vol.4
, pp. 562
-
-
Zolfigol, M.A.1
Shirini, F.2
Ghorbanichoghawarani, A.3
Mohammadpoor-Baltork, I.4
-
19
-
-
34548436430
-
Solvent-free one-pot synthesis of amidoalkyl naphthols catalyzed by silica sulfuric acid
-
(f) Hari, G. S.; Nagaraju, M.; Murthy, M. M. Solvent-free one-pot synthesis of amidoalkyl naphthols catalyzed by silica sulfuric acid. Helv. Chimica. Acta. 2007, 8, 1497.
-
(2007)
Helv. Chimica. Acta
, vol.8
, pp. 1497
-
-
Hari, G.S.1
Nagaraju, M.2
Murthy, M.M.3
-
20
-
-
0030031144
-
Sulfuric acid on silica-gel: An inexpensive catalyst for aromatic nitration
-
(a) Riego, J. M.; Sedin, Z.; Zaldivar, J. M.; Marziano, N. C.; Tortato, C. Sulfuric acid on silica-gel: an inexpensive catalyst for aromatic nitration. Tetrahedron Lett. 1996, 37, 513;
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 513
-
-
Riego, J.M.1
Sedin, Z.2
Zaldivar, J.M.3
Marziano, N.C.4
Tortato, C.5
-
21
-
-
0035851246
-
2 as a novel heterogeneous system for production of thionitrites and disulfides under mild conditions
-
2 as a novel heterogeneous system for production of thionitrites and disulfides under mild conditions. Tetrahedron 2001, 57, 9509.
-
(2001)
Tetrahedron
, vol.57
, pp. 9509
-
-
Zolfigol, M.A.1
-
22
-
-
0001322030
-
The reaction of nitroölefins with indole
-
(a) Noland, W. E.; Christensen, G. M.; Sauer, G. L. Dutton, G. G. S. The reaction of nitroölefins with indole. J. Am. Chem. Soc. 1995, 77, 456;
-
(1995)
J. Am. Chem. Soc
, vol.77
, pp. 456
-
-
Noland, W.E.1
Christensen, G.M.2
Sauer, G.L.3
Dutton, G.G.S.4
-
23
-
-
0000242844
-
Reactions on solid supports part IV: Reactions of αβ-unsaturated carbonyl compounds with indoles using clay as catalyst
-
(b) Iqbal, Z.; Jackson, A. H.; Rao, K. R. N. Reactions on solid supports part IV: Reactions of αβ-unsaturated carbonyl compounds with indoles using clay as catalyst. Tetrahedron Lett. 1988, 29, 2577.
-
(1988)
Tetrahedron Lett
, vol.29
, pp. 2577
-
-
Iqbal, Z.1
Jackson, A.H.2
Rao, K.R.N.3
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