-
1
-
-
57449121750
-
-
John Wiely & Sons, Inc., Hoboken, New Jersey pp 855
-
Wuts P.G.M., and Greene T.W. Greene's Protective Groups in Organic Synthesis. 4th ed. (2007), John Wiely & Sons, Inc., Hoboken, New Jersey pp 855
-
(2007)
Greene's Protective Groups in Organic Synthesis. 4th ed.
-
-
Wuts, P.G.M.1
Greene, T.W.2
-
4
-
-
0025129949
-
-
Jordis U., Sauter F., Siddiqi S.M., Küenburg B., and Bhattacharya K. Synthesis (1990) 925
-
(1990)
Synthesis
, pp. 925
-
-
Jordis, U.1
Sauter, F.2
Siddiqi, S.M.3
Küenburg, B.4
Bhattacharya, K.5
-
19
-
-
0001019782
-
-
Henry J.R., Marcin L.R., McIntosh M.C., Scola P.M., Harris Jr. G.D., and Weinreb S.M. Tetrahedron Lett. 30 (1989) 5709
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 5709
-
-
Henry, J.R.1
Marcin, L.R.2
McIntosh, M.C.3
Scola, P.M.4
Harris Jr., G.D.5
Weinreb, S.M.6
-
22
-
-
0001456215
-
-
Magnus P., Giles M., Bonnert R., Kim C.S., McQuire L., Merritt A., and Vicker N. J. Am. Chem. Soc. 114 (1992) 4403
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 4403
-
-
Magnus, P.1
Giles, M.2
Bonnert, R.3
Kim, C.S.4
McQuire, L.5
Merritt, A.6
Vicker, N.7
-
27
-
-
0342894825
-
-
Fukuyama T., Cheung M., Jow C.-K., Hidai Y., and Kan T. Tetrahedron Lett. 38 (1997) 5831
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 5831
-
-
Fukuyama, T.1
Cheung, M.2
Jow, C.-K.3
Hidai, Y.4
Kan, T.5
-
48
-
-
3242722926
-
-
Uchiyama M., Matsumoto Y., Nakamura S., Ohwada T., Kobayashi N., Yamashita N., Matsumiya A., and Sakammoto T. J. Am. Chem. Soc. 126 (2004) 8755
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8755
-
-
Uchiyama, M.1
Matsumoto, Y.2
Nakamura, S.3
Ohwada, T.4
Kobayashi, N.5
Yamashita, N.6
Matsumiya, A.7
Sakammoto, T.8
-
50
-
-
26844511376
-
-
Liu Q., Liu Z., Zhou Y.-L., Zhang W., Yang L., Liu Z.-L., and Yu W. Synlett (2005) 2510
-
(2005)
Synlett
, pp. 2510
-
-
Liu, Q.1
Liu, Z.2
Zhou, Y.-L.3
Zhang, W.4
Yang, L.5
Liu, Z.-L.6
Yu, W.7
-
59
-
-
58149154342
-
-
Liu Y., Shen L., Prashad M., Tibbatts J., Repič O., and Blacklock T.J. Org. Process Res. Dev. 12 (2008) 778
-
(2008)
Org. Process Res. Dev.
, vol.12
, pp. 778
-
-
Liu, Y.1
Shen, L.2
Prashad, M.3
Tibbatts, J.4
Repič, O.5
Blacklock, T.J.6
-
60
-
-
61349189648
-
-
Nandi P., Redko M.Y., Peterson K., Dye J.L., Lefenfeld M., Vogt P.F., and Jackson J.E. Org. Lett. 10 (2008) 5441
-
(2008)
Org. Lett.
, vol.10
, pp. 5441
-
-
Nandi, P.1
Redko, M.Y.2
Peterson, K.3
Dye, J.L.4
Lefenfeld, M.5
Vogt, P.F.6
Jackson, J.E.7
-
63
-
-
71049128147
-
-
Lund H., and Hammerich O. (Eds), Marcel Dekker, New York and references cited therein
-
Lund H. In: Lund H., and Hammerich O. (Eds). Organic Electrochemistry, Fourth Edition, Revised and Expanded. Clearvage and Deprotection (2001), Marcel Dekker, New York 969 and references cited therein
-
(2001)
Clearvage and Deprotection
, pp. 969
-
-
Lund, H.1
-
71
-
-
0004399653
-
-
Moriwaki T., Saito S., Tamai H., Fujita S., and Inaba M. Heterocycles 23 (1985) 2525
-
(1985)
Heterocycles
, vol.23
, pp. 2525
-
-
Moriwaki, T.1
Saito, S.2
Tamai, H.3
Fujita, S.4
Inaba, M.5
-
75
-
-
0002138568
-
-
Grehn L., Maia L.S., Monteiro L.S., Montenegro M.I., and Ragnarsson U. J. Chem. Res. (S) (1991) 144
-
(1991)
J. Chem. Res. (S)
, pp. 144
-
-
Grehn, L.1
Maia, L.S.2
Monteiro, L.S.3
Montenegro, M.I.4
Ragnarsson, U.5
-
76
-
-
27144519615
-
-
Scialdone O., Belfiore C., Filardo G., Galia A., Sabatino M.A., and Silvestri G. Electrochim. Acta 51 (2005) 598
-
(2005)
Electrochim. Acta
, vol.51
, pp. 598
-
-
Scialdone, O.1
Belfiore, C.2
Filardo, G.3
Galia, A.4
Sabatino, M.A.5
Silvestri, G.6
-
77
-
-
38349193431
-
-
Coeffard V., Thobie-Gautier C., Beaudet I., Le Grognec E., and Quintard J.-P. Eur. J. Org. Chem. (2008) 383
-
(2008)
Eur. J. Org. Chem.
, pp. 383
-
-
Coeffard, V.1
Thobie-Gautier, C.2
Beaudet, I.3
Le Grognec, E.4
Quintard, J.-P.5
-
79
-
-
71049129273
-
-
note
-
In the reaction of 3e in DMF, N-formyl-1,2,3,4-tetrahydro-6,7-dimethoxyisoquinoline was obtained in 72% yield. N-Dodecyl-N-methylformamide was also obtained in 52% yield along with 4f in 44% yield when the reaction of 3f was carried out in DMF.
-
-
-
-
82
-
-
71049160338
-
-
note
-
An excess electricity would be used for the reduction of N-H bond of mono-substituted tosylamide moiety in 5 resulting in generation of hydrogen and amide enolates.
-
-
-
|