-
3
-
-
0001585017
-
-
L. Bischoff, C. David, L. Martin, H. Meudal, B. P. Roques, M. C. Fournie-Zaluski, J. Org. Chem. 1997, 62, 4848.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4848
-
-
Bischoff, L.1
David, C.2
Martin, L.3
Meudal, H.4
Roques, B.P.5
Fournie-Zaluski, M.C.6
-
4
-
-
0036353846
-
-
a) R. Sanz, R. Aguado, M. R. Pedrosa, J. F. Arnaiz, Synthesis 2002, 856.
-
(2002)
Synthesis
, pp. 856
-
-
Sanz, R.1
Aguado, R.2
Pedrosa, M.R.3
Arnaiz, J.F.4
-
5
-
-
0005693463
-
-
b) W. A. Pryor, D. F. Church, C. K. Govindan, G. Crank, J. Org. Chem. 1982, 47, 156.
-
(1982)
J. Org. Chem.
, vol.47
, pp. 156
-
-
Pryor, W.A.1
Church, D.F.2
Govindan, C.K.3
Crank, G.4
-
8
-
-
0030066446
-
-
e) X. Wu, R. D. Rieke, L. Zhu, Synth. Commun. 1996, 26, 191.
-
(1996)
Synth. Commun.
, vol.26
, pp. 191
-
-
Wu, X.1
Rieke, R.D.2
Zhu, L.3
-
12
-
-
0042169029
-
-
i) A. T. S. Shah, M. K. Khan, M. Fecker, W. Voelter, Tetrahedron Lett. 2003, 44, 6789.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6789
-
-
Shah, A.T.S.1
Khan, M.K.2
Fecker, M.3
Voelter, W.4
-
16
-
-
2542461552
-
-
M. Hirao, S. Yakabe, H. Chikamori, J. H. Clark, T. Monmoto, J. Chem. Res. 1998, 310.
-
(1998)
J. Chem. Res.
, pp. 310
-
-
Hirao, M.1
Yakabe, S.2
Chikamori, H.3
Clark, J.H.4
Monmoto, T.5
-
20
-
-
0001516314
-
-
a) D. M. Tal, E. Keinan, Y. Mazur, Tetrahedron 1981, 37, 4327.
-
(1981)
Tetrahedron
, vol.37
, pp. 4327
-
-
Tal, D.M.1
Keinan, E.2
Mazur, Y.3
-
23
-
-
0028145274
-
-
a) F. Mohanazadeh, A. R. Momeni, Y. Ranjbar, Tetrahedron Lett. 1994, 35, 6127.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 6127
-
-
Mohanazadeh, F.1
Momeni, A.R.2
Ranjbar, Y.3
-
24
-
-
33646026731
-
-
b) M. Sathe, A. K. Gupta, M. P. Kaushik, Tetrahedron Lett. 2006, 47, 3107.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3107
-
-
Sathe, M.1
Gupta, A.K.2
Kaushik, M.P.3
-
25
-
-
33845268762
-
-
note
-
To a solution of alkane/arenethiol (1 mmol) in dichloromethane, silica chloride (5 mol %) was added at 0°C and access to atmospheric oxygen. The reaction mixture was stirred for 10 min; the progress of reaction was monitored by TLC and also by gas chromatography. After the completion of reaction, mixture was filtered off and filtrate was concentrated to afford dialkyl/aryl disulfide in a quantitative yield. The physical properties and NMR spectra of compounds agreed with those reported in the literature.
-
-
-
-
26
-
-
33845374912
-
-
Y. Kamitori, M. Hojo, R. Masuda, T. Kimura, T. Yoshida, J. Org. Chem. 1986, 51, 1427.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 1427
-
-
Kamitori, Y.1
Hojo, M.2
Masuda, R.3
Kimura, T.4
Yoshida, T.5
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