-
1
-
-
0000817070
-
-
Wiley: New York
-
(a) Wood, J. L. In Organic Reactions; Wiley: New York, 1967; Vol. III, pp. 240-266;
-
(1967)
Organic Reactions
, vol.3
, pp. 240-266
-
-
Wood, J.L.1
-
2
-
-
0027433854
-
Structure correction and synthesis of the naturally occurring benzothiazinone BMY 40662
-
(b) Kelly, T. R.; Kim, M. H.; Curtis, A. D. M. Structure correction and synthesis of the naturally occurring benzothiazinone BMY 40662. J. Org. Chem. 1993, 58, 5855.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 5855
-
-
Kelly, T.R.1
Kim, M.H.2
Curtis, A.D.M.3
-
4
-
-
0028928412
-
Thiocyanate as a versatile synthetic unit: Efficient conversion of ArSCN to aryl alkyl sulfides and aryl thioesters
-
(a) Toste, F. D.; LaRonde, F.; Still, I. W. J. Thiocyanate as a versatile synthetic unit: Efficient conversion of ArSCN to aryl alkyl sulfides and aryl thioesters. Tetrahedron Lett. 1995, 36, 2949;
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 2949
-
-
Toste, F.D.1
Laronde, F.2
Still, I.W.J.3
-
5
-
-
0141588652
-
Thiocyanation of indole: Some reactions of 3-thiocyanoindole
-
(b) Grant, M. S.; Snyder, H. R. Thiocyanation of indole: Some reactions of 3-thiocyanoindole. J. Am. Chem. Soc. 1960, 82, 2742;
-
(1960)
J. Am. Chem. Soc.
, vol.82
, pp. 2742
-
-
Grant, M.S.1
Snyder, H.R.2
-
6
-
-
34447279617
-
Microwave-assisted palladium-catalyzed regioselective cyanothiolation of alkynes with thiocyanates
-
(c) Lee, Y. T.; Choi, S. Y.; Chung, Y. K. Microwave-assisted palladium-catalyzed regioselective cyanothiolation of alkynes with thiocyanates. Tetrahedron Lett. 2007, 48, 5673.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 5673
-
-
Lee, Y.T.1
Choi, S.Y.2
Chung, Y.K.3
-
7
-
-
23044459885
-
Regioselective thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and oxone
-
Wu,G.; Liu, Q.; Shen, Y.;Wu, W.;Wu, L. Regioselective thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and oxone. Tetrahedron Lett. 2005, 46, 5831.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 5831
-
-
Wu, G.1
Liu, Q.2
Shen, Y.3
Wu, W.4
Wu, L.5
-
8
-
-
1642276015
-
Iodine=MeOH: A novel and efficient reagent system for thiocyanation of aromatics and heteroaromatics
-
Yadav, J. S.; Reddy, B. V. S.; Shubashree, S.; Sadashiv, K. Iodine=MeOH: A novel and efficient reagent system for thiocyanation of aromatics and heteroaromatics. Tetrahedron Lett. 2004, 45, 2951.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 2951
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Shubashree, S.3
Sadashiv, K.4
-
9
-
-
17744364542
-
Ferric(III) chloride-promoted electrophilic thiocyanation of aromatic and heteroaromatic compounds
-
Yadav, J. S.; Reddy, B. V. S.; Krishna, A. D.; Reddy, C. S.; Narsaiah, A. V. Ferric(III) chloride-promoted electrophilic thiocyanation of aromatic and heteroaromatic compounds. Synthesis 2005, 961.
-
(2005)
Synthesis
, vol.961
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Krishna, A.D.3
Reddy, C.S.4
Narsaiah, A.V.5
-
10
-
-
0028909777
-
A versatile procedure for the preparation of aryl thiocyanates using N-thiocyanatosuccinimide (NTS)
-
Toste, F. D.; Stefano, V. D.; Still, I. W. J. A versatile procedure for the preparation of aryl thiocyanates using N-thiocyanatosuccinimide (NTS). Synth. Commun. 1995, 25, 1277.
-
(1995)
Synth. Commun.
, vol.25
, pp. 1277
-
-
Toste, F.D.1
Stefano, V.D.2
Still, I.W.J.3
-
11
-
-
0033524666
-
A direct synthesis of aryl thiocyanates using cerium(IV) ammonium nitrate
-
Nair, V.; George, T. G.; Nair, L. G.; Panicker, S. B. A direct synthesis of aryl thiocyanates using cerium(IV) ammonium nitrate. Tetrahedron Lett. 1999, 40, 1195.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 1195
-
-
Nair, V.1
George, T.G.2
Nair, L.G.3
Panicker, S.B.4
-
12
-
-
0141768471
-
A clay-mediated ecofriendly thiocyanation of indoles and carbazoles
-
Chakrabarty, M.; Sarkar, S. A. A clay-mediated ecofriendly thiocyanation of indoles and carbazoles. Tetrahedron Lett. 2003, 44, 8131.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 8131
-
-
Chakrabarty, M.1
Sarkar, S.A.2
-
13
-
-
0001548384
-
Novel and direct nucleophilic sulfenylation and thiocyanation of phenol ethers using a hypervalent iodine(III) reagent
-
Kita, Y.; Takada, T.; Mihara, S.; Whelan, B. A.; Tohma, H. Novel and direct nucleophilic sulfenylation and thiocyanation of phenol ethers using a hypervalent iodine(III) reagent. J. Org. Chem. 1995, 60, 7144.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 7144
-
-
Kita, Y.1
Takada, T.2
Mihara, S.3
Whelan, B.A.4
Tohma, H.5
-
14
-
-
84859206625
-
Novel and efficient synthesis of sulfur-containing heterocycles using a hypervalent iodine(III) reagent
-
Kita, Y.; Takada, Y.; Okuno, T.; Egi, M.; Kiyosei, I.; Kawaguchi, C.; Akai, S. Novel and efficient synthesis of sulfur-containing heterocycles using a hypervalent iodine(III) reagent. Chem. Pharm. Bull. 1997, 45, 1887.
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 1887
-
-
Kita, Y.1
Takada, Y.2
Okuno, T.3
Egi, M.4
Kiyosei, I.5
Kawaguchi, C.6
Akai, S.7
-
15
-
-
18744409788
-
Efficient and mild oxidative nuclear thiocyanation of activated aromatic compounds using ammonium thiocyanate and diacetoxyiodobenzene
-
Karade, N. N.; Tiwari, G. B.; Shirodkar, S. G.; Dhoot, B. M. Efficient and mild oxidative nuclear thiocyanation of activated aromatic compounds using ammonium thiocyanate and diacetoxyiodobenzene. Synth. Commun. 2005, 35, 1197.
-
(2005)
Synth. Commun.
, vol.35
, pp. 1197
-
-
Karade, N.N.1
Tiwari, G.B.2
Shirodkar, S.G.3
Dhoot, B.M.4
-
16
-
-
38149031681
-
DDQ-promoted thiocyanation of aromatic and heteroaromatic compounds
-
(a) Memaian, H. R.; Mohammadpoor-Baltork, I.; Nikoofar, K. DDQ-promoted thiocyanation of aromatic and heteroaromatic compounds. Can. J. Chem. 2007, 85, 930;
-
(2007)
Can. J. Chem.
, vol.85
, pp. 930
-
-
Memaian, H.R.1
Mohammadpoor-Baltork, I.2
Nikoofar, K.3
-
17
-
-
44249092151
-
Ultrasound-assisted thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and DDQ
-
(b) Memaian, H. R.; Mohammadpoor-Baltork, I.; Nikoofar, K. Ultrasound-assisted thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and DDQ. Ultrason. Sonochem. 2008, 15, 456.
-
(2008)
Ultrason. Sonochem.
, vol.15
, pp. 456
-
-
Memaian, H.R.1
Mohammadpoor-Baltork, I.2
Nikoofar, K.3
-
18
-
-
67650299485
-
Facile method for thiocyanation of activated arenes using iodic acid in combination with ammonium thiocyanate
-
Mahajan, U. S.; Akamanchi, K. G. Facile method for thiocyanation of activated arenes using iodic acid in combination with ammonium thiocyanate. Synth. Commun. 2009, 39, 2674.
-
(2009)
Synth. Commun.
, vol.39
, pp. 2674
-
-
Mahajan, U.S.1
Akamanchi, K.G.2
-
19
-
-
57149143705
-
Mn(OAc)3-promoted regioselective free radical thiocyanation of indoles and anilines
-
Pan, X.-Q.; Lei, M.-Y.; Zou, J.-P.; Zhang, W. Mn(OAc)3-promoted regioselective free radical thiocyanation of indoles and anilines. Tetrahedron Lett. 2009, 50, 347.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 347
-
-
Pan, X.-Q.1
Lei, M.-Y.2
Zou, J.-P.3
Zhang, W.4
-
20
-
-
58149392372
-
Synthesis of aryl thiocyanates using Al2O3= MeSO3H (AMA) as a novel heterogeneous system
-
Hosseini Sarvari, M.; Tavakolian, M. Synthesis of aryl thiocyanates using Al2O3= MeSO3H (AMA) as a novel heterogeneous system. J. Chem. Res. 2008, 6, 318.
-
(2008)
J. Chem. Res.
, vol.6
, pp. 318
-
-
Hosseini Sarvari, M.1
Tavakolian, M.2
-
21
-
-
47249139524
-
Thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and I2O5
-
Wu, J.; Wu, G.; Wu, L. Thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and I2O5. Synth. Commun. 2008, 38, 2367.
-
(2008)
Synth. Commun.
, vol.38
, pp. 2367
-
-
Wu, J.1
Wu, G.2
Wu, L.3
-
22
-
-
57549097061
-
IBX: A novel and versatile oxidant for electrophilic thiocyanation of indoles, pyrroles, and aryl amines
-
Yadav, J. S.; Reddy, B. V. S.; Krishna, B. B. M. IBX: A novel and versatile oxidant for electrophilic thiocyanation of indoles, pyrroles, and aryl amines. Synthesis 2008, 3779.
-
(2008)
Synthesis
, vol.3779
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Krishna, B.B.M.3
-
23
-
-
77954242609
-
A new application for diethyl azodicarboxylate: Efficient and regioselective thiocyanation of aromatics amines
-
(a) Iranpoor, N.; Firouzabadi, H.; Khalili, D.; Rezvan, S. A new application for diethyl azodicarboxylate: Efficient and regioselective thiocyanation of aromatics amines. Tetrahedron Lett. 2010, 51, 3508;
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 3508
-
-
Iranpoor, N.1
Firouzabadi, H.2
Khalili, D.3
Rezvan, S.4
-
24
-
-
0037231022
-
Alkyl phosphines as reagents and catalysts in organic synthesis
-
and the reference cited therein
-
(b) Valentine, Jr. D. H.; Hillhouse, J. H. Alkyl phosphines as reagents and catalysts in organic synthesis. Synthesis 2003, 3, 317, and the reference cited therein.
-
(2003)
Synthesis
, vol.3
, pp. 317
-
-
Valentine Jr., D.H.1
Hillhouse, J.H.2
-
25
-
-
0141526368
-
Multistep redox sequences of azopyridyl (L) bridged reaction centres in stable radical complex ions f(m-L)[MCl(g5-C5Me5)]2g+, M=Rh or Ir: Spectroelectrochemistry and high-frequency EPR spectroscopy
-
2,20-azopyridine A1: Frantz
-
(a) 2,20-azopyridine A1: Frantz, S.; Reinhardt, R.; Greulich, S.; Wanner, M.; Fiedler, J.; Duboc-Toia, C.; Kaim, W. Multistep redox sequences of azopyridyl bridged reaction centres in stable radical complex ions f(m-L)[MCl(g5-C5Me5)]2g+, M=Rh or Ir: spectroelectrochemistry and high-frequency EPR spectroscopy. Dalton Trans. 2003, 3370.
-
(2003)
Dalton Trans.
, pp. 3370
-
-
Frantz, S.1
Reinhardt, R.2
Greulich, S.3
Wanner, M.4
Fiedler, J.5
Duboc-Toia, C.6
Kaim, W.7
-
26
-
-
1042288093
-
The syntheses, crystal structures, and optical limiting effects of HgI2 adduct polymers bridged by bipyridyl-based ligands
-
3,30-Azopyridine A2
-
3,30-Azopyridine A2: Niu, Y.; Song, Y.; Hou, H.; Zhu, Y. The syntheses, crystal structures, and optical limiting effects of HgI2 adduct polymers bridged by bipyridyl-based ligands. Inorg. Chim. Acta 2003, 335, 151.
-
(2003)
Inorg. Chim. Acta
, vol.335
, pp. 151
-
-
Niu, Y.1
Song, Y.2
Hou, H.3
Zhu, Y.4
-
27
-
-
46849097843
-
Easily prepared azopyridines as potent and recyclable reagents for facile esterification reactions. An efficient modified Mitsunobu reaction
-
4,40-Azopyridine A3
-
4,40-Azopyridine A3: (a) Iranpoor, N.; Firouzabadi, H.; Khalili, D.; Motevalli, S. Easily prepared azopyridines as potent and recyclable reagents for facile esterification reactions. An efficient modified Mitsunobu reaction. J. Org. Chem. 2008, 73, 4882;
-
(2008)
J. Org. Chem.
, vol.73
, pp. 4882
-
-
Iranpoor, N.1
Firouzabadi, H.2
Khalili, D.3
Motevalli, S.4
-
28
-
-
77955839027
-
New heteroaromatic azo compounds based on pyridine, isoxazole, and benzothiazole for efficient and highly selective amidation and mono-N-benzylation of amines under Mitsunobu conditions
-
(L) Iranpoor, N.; Firouzabadi, H.; Khalili, D. New heteroaromatic azo compounds based on pyridine, isoxazole, and benzothiazole for efficient and highly selective amidation and mono-N-benzylation of amines under Mitsunobu conditions. Bull. Chem. Soc. Jpn. 2010, 83, 923.
-
(2010)
Bull. Chem. Soc. Jpn.
, vol.83
, pp. 923
-
-
Iranpoor, N.1
Firouzabadi, H.2
Khalili, D.3
-
29
-
-
77956495503
-
5,50-Dimethyl-3,30-azoisoxazole as a new heterogeneous azo reagent for esterification of phenols and selective esterification of benzylic alcohols under Mitsunobu condition
-
Spectral data for A4: 1H NMR (250 MHz, CDCl3) d: 8.90-8.86 m, 6H). 13C NMR (62.9 MHz, CDCl3) d: 159.1, 157.5, 122.0. 5,50-Dimethyl-3,30-azoisoxazole A5
-
Spectral data for A4: 1H NMR (250 MHz, CDCl3) d: 8.90-8.86 m, 6H). 13C NMR (62.9 MHz, CDCl3) d: 159.1, 157.5, 122.0. 5,50-Dimethyl-3,30-azoisoxazole A5: Iranpoor, N.; Firouzabadi, H.; Khalili, D. 5,50-Dimethyl-3,30-azoisoxazole as a new heterogeneous azo reagent for esterification of phenols and selective esterification of benzylic alcohols under Mitsunobu condition. Org. Biomol. Chem. 2010, 8, 4436.
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 4436
-
-
Iranpoor, N.1
Firouzabadi, H.2
Khalili, D.3
-
30
-
-
0037380135
-
Synthesis and properties of bis(hetaryl)azo dyes
-
2,20-Azobenzothiazole A6
-
2,20-Azobenzothiazole A6: Wang, M.; Funabiki, K.; Matsui, M. Synthesis and properties of bis(hetaryl)azo dyes. Dyes Pigm. 2003, 57, 77.
-
(2003)
Dyes Pigm.
, vol.57
, pp. 77
-
-
Wang, M.1
Funabiki, K.2
Matsui, M.3
|