-
1
-
-
0348048819
-
On the role of triflic acid in the metal triflate catalysed acylation of alcohols
-
Dumeunier, R.; Marko, I. E. On the role of triflic acid in the metal triflate catalysed acylation of alcohols. Tetrahedron Lett. 2004, 45, 825.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 825
-
-
Dumeunier, R.1
Marko, I.E.2
-
2
-
-
0003463148
-
Protective groups
-
3rd ed, John Wiley and sons: New York
-
Greene, T. W.; Wuts, P. G. M. Protective groups; In Organic Synthesis, 3rd ed.; John Wiley and sons: New York, 1999; p. 36.
-
(1999)
Organic Synthesis
, pp. 36
-
-
Greene, T.W.1
Wuts, P.G.M.2
-
3
-
-
6844222490
-
The reactions of aliphatic acid chlorides
-
Norman, O. V.; Sonntag. The reactions of aliphatic acid chlorides. Chem. Rev. 1953, 52, 237.
-
(1953)
Chem. Rev
, vol.52
, pp. 237
-
-
Norman, O.V.1
Sonntag2
-
5
-
-
0002799045
-
A convenient method for the synthesis of carboxamides and peptides by the use of tetrabutyl ammonium salt
-
Watanabe, Y.; Miyamoto, K.; Kiji. A convenient method for the synthesis of carboxamides and peptides by the use of tetrabutyl ammonium salt. J. Chem. Lett. 1981, 285.
-
(1981)
J. Chem. Lett
, pp. 285
-
-
Watanabe, Y.1
Miyamoto, K.2
Kiji3
-
6
-
-
33845283356
-
Cyanide as an efficient and mild catalyst in the aminolysis of esters
-
(a) Hogberg, T.; Strom, P.; Ebner, M.; Ramsby, S. Cyanide as an efficient and mild catalyst in the aminolysis of esters. J. Org. Chem. 1987, 52, 2033;
-
(1987)
J. Org. Chem
, vol.52
, pp. 2033
-
-
Hogberg, T.1
Strom, P.2
Ebner, M.3
Ramsby, S.4
-
7
-
-
67650289796
-
Iodine catalysed synthesis of b-keto enol ethers
-
(b) Chen, S.-J.; Chen, S.-T.; Chen, S.-Y.; Wang, K. T. Iodine catalysed synthesis of b-keto enol ethers. Tetrahedron Lett. 1994, 35, 3588.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 3588
-
-
Chen, S.-J.1
Chen, S.-T.2
Chen, S.-Y.3
Wang, K.T.4
-
9
-
-
0037284158
-
Molecular iodinecatalysed highly stereoselective synthesis of sugar acetylenes
-
(a) Yadav, J. S.; Reddy, B. V. S.; Rao, C. V.; Reddy, M. S. Molecular iodinecatalysed highly stereoselective synthesis of sugar acetylenes. Synthesis 2003, 247;
-
(2003)
Synthesis
, pp. 247
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Rao, C.V.3
Reddy, M.S.4
-
10
-
-
0036257513
-
Iodine-catalyzed, efficient and mild procedure for highly chemoselective acetalization of carbonyl compounds under neutral aprotic conditions
-
(b) Karimi, B.; Golshani, B. Iodine-catalyzed, efficient and mild procedure for highly chemoselective acetalization of carbonyl compounds under neutral aprotic conditions. Synthesis 2002, 784;
-
(2002)
Synthesis
, pp. 784
-
-
Karimi, B.1
Golshani, B.2
-
11
-
-
0036343682
-
Synthesis of 3H pyrroles promoted by samarium=catalysed iodine system
-
(c) Xu, X.; Zhang, Y. Synthesis of 3H pyrroles promoted by samarium=catalysed iodine system. Synthetic Commun. 2002, 32, 2643
-
(2002)
Synthetic Commun
, vol.32
, pp. 2643
-
-
Xu, X.1
Zhang, Y.2
-
12
-
-
2442691603
-
Iodine as a very powerful catalyst for three-component synthesis of protected homoallylic amines
-
(d) Phukan, P. Iodine as a very powerful catalyst for three-component synthesis of protected homoallylic amines. J. Org. Chem.2004, 69, 4005-4006.
-
(2004)
J. Org. Chem
, vol.69
, pp. 4005-4006
-
-
Phukan, P.1
-
13
-
-
1842585835
-
Aldol reactions of silyl enolates catalyzed by iodine
-
Phukan, P. M. Aldol reactions of silyl enolates catalyzed by iodine. Synthetic Commun. 2004, 34, 1065.
-
(2004)
Synthetic Commun
, vol.34
, pp. 1065
-
-
Phukan, P.M.1
-
14
-
-
2442701279
-
Iodine as extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions
-
Phukan, P. Iodine as extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions. Tetrahedron Lett. 2004, 45, 4785-4787.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 4785-4787
-
-
Phukan, P.1
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