-
3
-
-
0001094662
-
Glycobiology: Toward understanding the function of sugars
-
(a) Dwek, R.A. Glycobiology: toward understanding the function of sugars. Chem. Rev., 1996, 96, 683-720.
-
(1996)
Chem. Rev.
, vol.96
, pp. 683-720
-
-
Dwek, R.A.1
-
4
-
-
0036462604
-
Synthesis of glycoproteins
-
(b) Davis, B.G. Synthesis of glycoproteins. Chem. Rev., 2002, 102, 579-601
-
(2002)
Chem. Rev.
, vol.102
, pp. 579-601
-
-
Davis, B.G.1
-
5
-
-
5244279498
-
Recent progress in O-glycosylation methods and its application to natural products synthesis
-
(c) Toshima, K.; Tatsuta, K. Recent progress in O-glycosylation methods and its application to natural products synthesis. Chem. Rev., 1993, 93, 1503-1531.
-
(1993)
Chem. Rev.
, vol.93
, pp. 1503-1531
-
-
Toshima, K.1
Tatsuta, K.2
-
7
-
-
11144256407
-
Gadolinium triflate: An efficient and convenient catalyst for acetylation of alcohols and amines
-
(b) Alleti, R.; Perambuduru, M.; Samantha, S.; Reddy V.P. Gadolinium triflate: an efficient and convenient catalyst for acetylation of alcohols and amines. J. Mol. Catal. A: Chem., 2005, 226, 57-59.
-
(2005)
J. Mol. Catal. A: Chem.
, vol.226
, pp. 57-59
-
-
Alleti, R.1
Perambuduru, M.2
Samantha, S.3
Reddy, V.P.4
-
8
-
-
0037940236
-
Lithium Trifluoromethanesulfonate (LiOTf) as a Recyclable Catalyst for Highly Efficient Acetylation of Alcohols and Diacetylation of Aldehydes under Mild and Neutral Reaction Conditions
-
(c) Karimi, B.; Maleki, J. Lithium Trifluoromethanesulfonate (LiOTf) as a Recyclable Catalyst for Highly Efficient Acetylation of Alcohols and Diacetylation of Aldehydes under Mild and Neutral Reaction Conditions. J. Org. Chem., 2003, 68, 4951-4954.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 4951-4954
-
-
Karimi, B.1
Maleki, J.2
-
9
-
-
85039825689
-
5-catalyzed Biginelli reaction: One-pot synthesis of 3, 4-dihydropyrimidin-2-(1H)-ones/thiones under solvent-free conditions
-
5-catalyzed Biginelli reaction: one-pot synthesis of 3, 4-dihydropyrimidin-2-(1H)-ones/thiones under solvent-free conditions. Tetrahedron Lett., 2006, 47, 53-49.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 53-49
-
-
Ahmed, N.1
Van Lier, J.E.2
-
10
-
-
33747879769
-
A novel 3-nitrobenzeneboronic acid as an extremely mild and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions
-
(e) Tale, R.H.; Adude, R.N. A novel 3-nitrobenzeneboronic acid as an extremely mild and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions. Tetrahedron Lett., 2006, 47, 7263-7265.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 7263-7265
-
-
Tale, R.H.1
Adude, R.N.2
-
11
-
-
33747163923
-
2O as a catalyst under solvent-free conditions
-
2O as a catalyst under solvent-free conditions. Tetrahedron Lett., 2006, 47, 6825-6829.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 6825-6829
-
-
Reddy, T.S.1
Narasimhulu, M.2
Suryakiran, N.3
Mahesh, K.C.4
Ashalatha, K.5
Venkateswarlu, Y.6
-
12
-
-
2442701279
-
Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions
-
(g) Phukan, P. Iodine as an 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
-
13
-
-
0037492241
-
Highly efficient and versatile acetylation of alcohols catalyzed by cerium (III) triflate
-
(h) Dalpozzo, R.; De Nino, A.; Maiuolo, L.; Procopio, A.; Nardi, M.; Bartoli, G.; Romeo, R. Highly efficient and versatile acetylation of alcohols catalyzed by cerium (III) triflate. Tetrahedron Lett., 2003, 44, 5621-5624.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 5621-5624
-
-
Dalpozzo, R.1
De Nino, A.2
Maiuolo, L.3
Procopio, A.4
Nardi, M.5
Bartoli, G.6
Romeo, R.7
-
14
-
-
34247582284
-
3 as a highly efficient catalyst for the rapid acetylation of alcohols, phenols and thiophenols under solvent-free conditions
-
3 as a highly efficient catalyst for the rapid acetylation of alcohols, phenols and thiophenols under solvent-free conditions. Tetrahedron Lett., 2007, 48, 3813-3828.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 3813-3828
-
-
Kamal, A.1
Khan, M.N.A.2
Reddy, K.S.3
Srikanth, Y.V.V.4
Krishnaji, T.5
-
15
-
-
13444263493
-
Cobalt (II)-catalyzed direct acetylation of alcohols with acetic acid
-
(j) Velusamy, S.; Borpuzari, S.; Punniyamurthy, T. Cobalt (II)-catalyzed direct acetylation of alcohols with acetic acid. Tetrahedron Lett., 2005, 61, 2011-2015.
-
(2005)
Tetrahedron Lett.
, vol.61
, pp. 2011-2015
-
-
Velusamy, S.1
Borpuzari, S.2
Punniyamurthy, T.3
-
16
-
-
0345168771
-
2 as a powerful catalyst for the acylation of alcohols under solvent-free conditions
-
2 as a powerful catalyst for the acylation of alcohols under solvent-free conditions. Eur. J. Org. Chem., 2003, 03, 4611-4617.
-
(2003)
Eur. J. Org. Chem.
, vol.3
, pp. 4611-4617
-
-
Bartoli, G.1
Bosco, M.2
Dalpozzo, R.3
Marcantoni, E.4
Massaccesi, M.5
Sambri, L.6
-
17
-
-
85039826731
-
Succinimide-N-sulfonic acid: An efficient catalyst for the synthesis of xanthene derivatives under solvent-free conditions
-
(l) Ghaffari Khaligh, N. Succinimide-N-sulfonic acid: an efficient catalyst for the synthesis of xanthene derivatives under solvent-free conditions. J. Mol. Catal. A: Chem., 2012, 90, 363-364.
-
(2012)
J. Mol. Catal. A: Chem.
, vol.90
, pp. 363-364
-
-
Ghaffari Khaligh, N.1
-
18
-
-
57149121902
-
A heterogeneous cobalt (II) Salen complex as an efficient and reusable catalyst for acetylation of alcohols and phenols
-
(m) Rajabi, F. A heterogeneous cobalt (II) Salen complex as an efficient and reusable catalyst for acetylation of alcohols and phenols. Tetrahedron Lett., 2009, 50, 395-397.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 395-397
-
-
Rajabi, F.1
-
19
-
-
84860835118
-
Borated zirconia modified with ammonium metatungstate as catalyst in alcohol acetylation
-
(n) Osiglio, L.; Sathicq, A.G.; Romanelli, G.P.; Blanco M.N. Borated zirconia modified with ammonium metatungstate as catalyst in alcohol acetylation. J.Mol. Catal. A: Chem., 2012, 359-362.
-
(2012)
J.Mol. Catal. A: Chem.
, pp. 359-362
-
-
Osiglio, L.1
Sathicq, A.G.2
Romanelli, G.P.3
Blanco, M.N.4
-
20
-
-
79957586724
-
Task-oriented use of ionic liquids: Efficient acetylation of alcohols and phenols
-
(o) López, I.; Bravo, J.L.; Caraballo, M.; Barneto, J.L.; Silvero, G. Task-oriented use of ionic liquids: efficient acetylation of alcohols and phenols. Tetrahedron Lett., 2011, 52, 3339-3341.
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 3339-3341
-
-
López, I.1
Bravo, J.L.2
Caraballo, M.3
Barneto, J.L.4
Silvero, G.5
-
21
-
-
84981783095
-
N, N dimethyl 4 pyridinamine, a very effective acylation catalyst
-
(a) Steglich, W.; Höfle, G. N, N dimethyl 4 pyridinamine, a very effective acylation catalyst. Angew. Chem. Int. Ed., 1969, 8, 981.
-
(1969)
Angew. Chem. Int. Ed.
, vol.8
, pp. 981
-
-
Steglich, W.1
Höfle, G.2
-
22
-
-
80051729483
-
Tributylphosphine: A remarkable acylation catalyst
-
(b) Vedejs, E.; Diver, S.T. Tributylphosphine: a remarkable acylation catalyst. J. Am. Chem. Soc., 1993, 115, 3358-3359
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 3358-3359
-
-
Vedejs, E.1
Diver, S.T.2
-
23
-
-
0345374581
-
Highly efficient acylation of alcohols, amines and thiols under solvent-free and catalyst-free conditions
-
Ranu, B.C.; Dey, S.S.; Hajra A. Highly efficient acylation of alcohols, amines and thiols under solvent-free and catalyst-free conditions, Green Chem., 2003, 5, 44-46.
-
(2003)
Green Chem.
, vol.5
, pp. 44-46
-
-
Ranu, B.C.1
Dey, S.S.2
Hajra, A.3
-
24
-
-
18044397338
-
3 as a powerful catalyst for the acetylation of carbohydrate alcohols under microwave irradiation
-
3 as a powerful catalyst for the acetylation of carbohydrate alcohols under microwave irradiation. Carbohydr. Res., 2005, 340, 1387-1392
-
(2005)
Carbohydr. Res.
, vol.340
, pp. 1387-1392
-
-
Das, S.K.1
Reddy, K.A.2
Krovvidi, V.3
Mukkanti, K.4
-
25
-
-
0034905861
-
Chemoselective acetylation of alcohols, amines, and thiols without catalyst and solvent
-
(b) Bandgar, B.P.; Kasture, S.P.; Kamble, V.T. Chemoselective acetylation of alcohols, amines, and thiols without catalyst and solvent. Synth. Commun., 2001, 31, 2255-2259.
-
(2001)
Synth. Commun.
, vol.31
, pp. 2255-2259
-
-
Bandgar, B.P.1
Kasture, S.P.2
Kamble, V.T.3
-
26
-
-
0347090500
-
Ultrasound promoted acetylation of alcohols in room temperature ionic liquid under ambient conditions
-
Gholap, A.R.; Venkatesan, K.; Daniel, T.; Lahoti, R.J.; Srinivasan, K.V., Ultrasound promoted acetylation of alcohols in room temperature ionic liquid under ambient conditions. Green Chem., 2003, 5, 693-696.
-
(2003)
Green Chem.
, vol.5
, pp. 693-696
-
-
Gholap, A.R.1
Venkatesan, K.2
Daniel, T.3
Lahoti, R.J.4
Srinivasan, K.V.5
-
27
-
-
57149121902
-
A heterogeneous cobalt (II) Salen complex as an efficient and reusable catalyst for acetylation of alcohols and phenols
-
(a) Rajabi, F. A heterogeneous cobalt (II) Salen complex as an efficient and reusable catalyst for acetylation of alcohols and phenols. Tetrahedron Lett., 2009, 4, 395-397.
-
(2009)
Tetrahedron Lett.
, vol.4
, pp. 395-397
-
-
Rajabi, F.1
-
28
-
-
58149402214
-
3) nanopowder prepared by sucrose-assisted combustion method: A novel and reusable heterogeneous catalyst for acetylation of amines, alcohols and phenols under solvent-free conditions
-
3) nanopowder prepared by sucrose-assisted combustion method: A novel and reusable heterogeneous catalyst for acetylation of amines, alcohols and phenols under solvent-free conditions. J. Mol. Catal. A., 2009, 299, 18-25.
-
(2009)
J. Mol. Catal. A.
, vol.299
, pp. 18-25
-
-
Farhadi, S.1
Zaidi, M.2
-
29
-
-
41649090535
-
Polymer-supported gadolinium triflate as a convenient and efficient Lewis acid catalyst for acetylation of alcohols and phenols
-
(c) Yoon, H.J.; Lee, S.M.; Kim, J.H. Polymer-supported gadolinium triflate as a convenient and efficient Lewis acid catalyst for acetylation of alcohols and phenols. Tetrahedron Lett., 2008, 49, 3165-3171.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 3165-3171
-
-
Yoon, H.J.1
Lee, S.M.2
Kim, J.H.3
-
30
-
-
33947311361
-
3 as a highly efficient and recyclable heterogeneous catalyst for the chemoselective acetylation of alcohols, phenols amines and thiols with acetic anhydride under solvent free conditions
-
3 as a highly efficient and recyclable heterogeneous catalyst for the chemoselective acetylation of alcohols, phenols amines and thiols with acetic anhydride under solvent free conditions. J. Mol. Catal. A., 2007, 267, 108-111.
-
(2007)
J. Mol. Catal. A.
, vol.267
, pp. 108-111
-
-
Joseph, J.K.1
Jain, S.L.2
Sain, B.3
-
31
-
-
37349023964
-
Selective Acetylation of Alcohols, Phenols and Amines and Selective Deprotection of Aromatic Acetates using Silica-Supported Phosphomolybdic Acid
-
(e) Das, B.; Thirupathi, P.; Kumar, P.; Laxminarayana, K. Selective Acetylation of Alcohols, Phenols and Amines and Selective Deprotection of Aromatic Acetates using Silica-Supported Phosphomolybdic Acid. Adv. Synth. Catal., 2007, 349, 2677-2683.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 2677-2683
-
-
Das, B.1
Thirupathi, P.2
Kumar, P.3
Laxminarayana, K.4
-
33
-
-
34248229294
-
40] as the catalyst
-
40] as the catalyst. Monatsh. Chem., 2007, 138, 445-447.
-
(2007)
Monatsh. Chem.
, vol.138
, pp. 445-447
-
-
Heravi, M.M.1
Bakhtiari, K.2
Javadi, N.M.3
Oskooie, H.A.4
Bamoharram, F.F.5
-
34
-
-
33747879769
-
A novel 3-nitrobenzeneboronic acid as an extremely mild and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions
-
(c) Tale, R.H.; Adude, R.N. A novel 3-nitrobenzeneboronic acid as an extremely mild and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions. Tetrahedron Lett., 2006 47, 7263-7265.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 7263-7265
-
-
Tale, R.H.1
Adude, R.N.2
-
35
-
-
46449084869
-
Immobilized Manihot esculenta preparation as a novel biocatalyst in the enantioselective acetylation of racemic alcohols
-
(a) Machado, L.L.; Lemos, T.; de Mattos, M. Immobilized Manihot esculenta preparation as a novel biocatalyst in the enantioselective acetylation of racemic alcohols. Tetrahedron Asymm., 2008, 19, 1418-1423.
-
(2008)
Tetrahedron Asymm.
, vol.19
, pp. 1418-1423
-
-
Machado, L.L.1
Lemos, T.2
De Mattos, M.3
-
36
-
-
35148825990
-
Enzymatic resolution of ethyl 3-hydroxy-2 (1' substituted-methylidene)-butyrate by Pseudomonas cepacia lipase catalyzed acetylation
-
(b) Benfatti, F.; Cardillo, G.; Gentilucci, L.; Mosconi, E.; Tolomelli, A., Enzymatic resolution of ethyl 3-hydroxy-2 (1' substituted-methylidene)-butyrate by Pseudomonas cepacia lipase catalyzed acetylation. Tetrahedron Asymm., 2007, 18, 2227-2232.
-
(2007)
Tetrahedron Asymm.
, vol.18
, pp. 2227-2232
-
-
Benfatti, F.1
Cardillo, G.2
Gentilucci, L.3
Mosconi, E.4
Tolomelli, A.5
-
37
-
-
38349154105
-
4] ionic liquid as novel catalyst for the rapid acetylation of alcohols, hydroxyesters and phenols under solvent-free conditions
-
4] ionic liquid as novel catalyst for the rapid acetylation of alcohols, hydroxyesters and phenols under solvent-free conditions. J. Catal. Lett., 2008, 121, 77-80.
-
(2008)
J. Catal. Lett.
, vol.121
, pp. 77-80
-
-
Wang, W.1
Cheng, W.2
Shao, W.3
Yang, W.4
-
38
-
-
44549084498
-
An imidazolium tosylate salt as efficient and recyclable catalyst for acetylation in an ionic liquid
-
(b) Liu, Y.; Liu, L.; Lu, Y.; Cai, Y.Q. An imidazolium tosylate salt as efficient and recyclable catalyst for acetylation in an ionic liquid. Monatsh. Chem., 2008, 139, 633-638.
-
(2008)
Monatsh. Chem.
, vol.139
, pp. 633-638
-
-
Liu, Y.1
Liu, L.2
Lu, Y.3
Cai, Y.Q.4
-
39
-
-
0037035324
-
Rapid, clean, and mild O-acetylation of alcohols and carbohydrates in an ionic liquid
-
(c) Forsyth, S.A.; MacFarlane, D.R.; Thomson, R.J.; von Itzsein, M. Rapid, clean, and mild O-acetylation of alcohols and carbohydrates in an ionic liquid. Chem. Commun., 2002, 714-715.
-
(2002)
Chem. Commun.
, pp. 714-715
-
-
Forsyth, S.A.1
MacFarlane, D.R.2
Thomson, R.J.3
Von Itzsein, M.4
-
40
-
-
13144305074
-
Industrial application of ionic liquids as performance additives
-
(a) Weyershausen, B.; Lehmann, K.; Industrial application of ionic liquids as performance additives. Green Chem., 2005, 7, 15-19.
-
(2005)
Green Chem.
, vol.7
, pp. 15-19
-
-
Weyershausen, B.1
Lehmann, K.2
-
41
-
-
19744376351
-
Industrial application of ionic liquids as process aid
-
(b) Weyershausen, B.; Hell, K.; Hesse, U. Industrial application of ionic liquids as process aid. Green Chem., 2005, 7, 283-287.
-
(2005)
Green Chem.
, vol.7
, pp. 283-287
-
-
Weyershausen, B.1
Hell, K.2
Hesse, U.3
-
42
-
-
33745629393
-
Preparation of simple ammonium ionic liquids and their application in the cracking of dialkoxypropanes
-
(a) Wang, C.; Guo, L.; Li, H.; Wang, Y.; Weng, J.; Wu, L. Preparation of simple ammonium ionic liquids and their application in the cracking of dialkoxypropanes. Green Chem., 2006, 8, 603-607.
-
(2006)
Green Chem.
, vol.8
, pp. 603-607
-
-
Wang, C.1
Guo, L.2
Li, H.3
Wang, Y.4
Weng, J.5
Wu, L.6
-
43
-
-
33645387033
-
Novel quaternary ammonium ionic liquids and their use as dual solvent-catalysts in the hydrolytic reaction
-
(b) Weng, J.; Wang, C.; Li, H.; Wang, Y. Novel quaternary ammonium ionic liquids and their use as dual solvent-catalysts in the hydrolytic reaction. Green Chem., 2006, 8, 96-99.
-
(2006)
Green Chem.
, vol.8
, pp. 96-99
-
-
Weng, J.1
Wang, C.2
Li, H.3
Wang, Y.4
-
44
-
-
33751366817
-
Preparation of dialkoxypropanes in simple ammonium ionic liquids
-
(c) Jiang, H.; Wang, C.; Li, H.; Wang, Y. Preparation of dialkoxypropanes in simple ammonium ionic liquids. Green Chemistry, 2006, 8, 1076-1079.
-
(2006)
Green Chemistry
, vol.8
, pp. 1076-1079
-
-
Jiang, H.1
Wang, C.2
Li, H.3
Wang, Y.4
-
45
-
-
33846527339
-
Application of triethylammonium salts as ionic liquid catalyst and medium for Fischer esterification
-
(d) Ganeshpure, P.A.; George, G.; Das, J. Application of triethylammonium salts as ionic liquid catalyst and medium for Fischer esterification. Arkivoc., 2007, 8, 273-278.
-
(2007)
Arkivoc.
, vol.8
, pp. 273-278
-
-
Ganeshpure, P.A.1
George, G.2
Das, J.3
-
46
-
-
50949099123
-
Triethylammonium acetate (TEAA): A recyclable inexpensive ionic liquid promotes the chemoselective aza-and thia-Michael reactions
-
(e) Verma, A.K.; Attri, P.; Chopra, V.; Tiwari, R.K.; Chandra, R. Triethylammonium acetate (TEAA): a recyclable inexpensive ionic liquid promotes the chemoselective aza-and thia-Michael reactions. Monatsh. Chem., 2008, 139, 1041-1047.
-
(2008)
Monatsh. Chem.
, vol.139
, pp. 1041-1047
-
-
Verma, A.K.1
Attri, P.2
Chopra, V.3
Tiwari, R.K.4
Chandra, R.5
-
47
-
-
79954523004
-
Triethylammonium Acetate [TEAA]: An Efficient Catalyst for One Pot Synthesis of Tetrahydro-4H-chromene Derivatives
-
(f) Balaskar, R.; Gavade, S.; Mane, M.; Pabrekar, P.; Shingare, M.; Mane, D. Triethylammonium Acetate [TEAA]: An Efficient Catalyst for One Pot Synthesis of Tetrahydro-4H-chromene Derivatives. Lett. Org. Chem., 2011, 8, 282-286.
-
(2011)
Lett. Org. Chem.
, vol.8
, pp. 282-286
-
-
Balaskar, R.1
Gavade, S.2
Mane, M.3
Pabrekar, P.4
Shingare, M.5
Mane, D.6
-
48
-
-
80051871019
-
Triethylammonium Acetate [TEAA]: An Efficient Catalyst for One Pot Synthesis of Tetrahydro-4H-Chromene Derivatives
-
(g) Dhananjay, M. Triethylammonium Acetate [TEAA]: An Efficient Catalyst for One Pot Synthesis of Tetrahydro-4H-Chromene Derivatives. Res. J. Chem. Environ., 2011, 15, 160-163.
-
(2011)
Res. J. Chem. Environ.
, vol.15
, pp. 160-163
-
-
Dhananjay, M.1
-
49
-
-
84877782976
-
Triethylammonium acetate-mediated domino-Knoevenagel-hetero-Diels-Alder reaction: Synthesis of some angular polyheterocycles
-
(h) Parmar, N.J.; Pansuriya, B.R.; Barad, H.A.; Parmar, B.D.; Kant, R.; Gupta, V.K. Triethylammonium acetate-mediated domino-Knoevenagel-hetero-Diels-Alder reaction: synthesis of some angular polyheterocycles. Monatsh. Chem., 2013, 144, 865-878.
-
(2013)
Monatsh. Chem.
, vol.144
, pp. 865-878
-
-
Parmar, N.J.1
Pansuriya, B.R.2
Barad, H.A.3
Parmar, B.D.4
Kant, R.5
Gupta, V.K.6
-
50
-
-
78651075252
-
4 nanoparticles: A magnetically recoverable catalyst for selective deacetylation of carbohydrate derivatives
-
4 nanoparticles: A magnetically recoverable catalyst for selective deacetylation of carbohydrate derivatives. Top. Catal., 2010, 53, 1087-1090.
-
(2010)
Top. Catal.
, vol.53
, pp. 1087-1090
-
-
Tasca, J.E.1
Ponzinibbio, A.2
Diaz, G.3
Bravo, R.D.4
Lavat, A.5
Gonzalez, M.G.6
-
51
-
-
84866727375
-
pTSA/[bmim][BF4] Ionic Liquid: A Powerful Recyclable Catalytic System for the Synthesis of α-2-Deoxyglycosides
-
(b) Diaz, G.; Ponzinibbio, A.; Bravo, R.D. pTSA/[bmim][BF4] Ionic Liquid: A Powerful Recyclable Catalytic System for the Synthesis of α-2-Deoxyglycosides. Top. Catal., 2012, 55, 644-648.
-
(2012)
Top. Catal.
, vol.55
, pp. 644-648
-
-
Diaz, G.1
Ponzinibbio, A.2
Bravo, R.D.3
-
52
-
-
84902013333
-
Synthesis of novel 2-deoxy-β-benzyl-C-glycosides by highly stereo and chemoselective hydrogenation of exo-glycals
-
(c) Díaz, G.; Ponzinibbio, A.; Bravo, R.D. Synthesis of novel 2-deoxy-β-benzyl-C-glycosides by highly stereo and chemoselective hydrogenation of exo-glycals. Carbohydr. Res., 2014, 393, 23-25.
-
(2014)
Carbohydr. Res.
, vol.393
, pp. 23-25
-
-
Díaz, G.1
Ponzinibbio, A.2
Bravo, R.D.3
-
54
-
-
84981783095
-
N dimethyl 4 pyridinamine, a very effective acylation catalyst
-
Steglich, W.; Hofle, G.N. N dimethyl 4 pyridinamine, a very effective acylation catalyst. Angew. Chem., Int. Ed. Engl., 1969, 8, 981-985.
-
(1969)
Angew. Chem., Int. Ed. Engl.
, vol.8
, pp. 981-985
-
-
Steglich, W.1
Hofle, G.N.2
-
56
-
-
0008866853
-
The intermediacy of sulfate esters in sulfuric acid catalyzed acetylation of carbohydrates
-
Hyatt, J.A.; Tindall, G.W. The intermediacy of sulfate esters in sulfuric acid catalyzed acetylation of carbohydrates. Heterocycles, 1993, 35, 227-234.
-
(1993)
Heterocycles
, vol.35
, pp. 227-234
-
-
Hyatt, J.A.1
Tindall, G.W.2
-
57
-
-
0031800609
-
Chemical synthesis of GDP-L-galactose and analogues
-
Binch, H.; Stangier, K.; Thiem, J. Chemical synthesis of GDP-L-galactose and analogues. Carbohydr. Res., 1998, 306, 409-419.
-
(1998)
Carbohydr. Res.
, vol.306
, pp. 409-419
-
-
Binch, H.1
Stangier, K.2
Thiem, J.3
-
58
-
-
0037185514
-
3-catalyzed acetolysis of 1,6-anhydro-β-hexopyranoses and solvent-free per-acetylation of hexoses
-
3-catalyzed acetolysis of 1,6-anhydro-β-hexopyranoses and solvent-free per-acetylation of hexoses. Tetrahedron Lett., 2002, 43, 851-855.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 851-855
-
-
Lee, J.C.1
Tai, C.A.2
Hung, S.C.3
-
59
-
-
0000073239
-
An extremely powerful acylation reaction of alcohols with acid anhydrides catalyzed by trimethylsilyl trifluoromethanesulfonate
-
(b) Procopiou, P.A.; Baugh, S.P.D.; Flack, S.S.; Inglis, G.G.A. An extremely powerful acylation reaction of alcohols with acid anhydrides catalyzed by trimethylsilyl trifluoromethanesulfonate. J. Org. Chem., 1998, 63, 2342-2347.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 2342-2347
-
-
Procopiou, P.A.1
Baugh, S.P.D.2
Flack, S.S.3
Inglis, G.G.A.4
-
60
-
-
0032753189
-
Indium triflate: An efficient catalyst for acylation reactions
-
(c) Chauhan, K.K.; Frost, C.G.; Love, I.; Waite, D. Indium triflate: an efficient catalyst for acylation reactions. Synlett., 1999, 1743-1744.
-
(1999)
Synlett.
, pp. 1743-1744
-
-
Chauhan, K.K.1
Frost, C.G.2
Love, I.3
Waite, D.4
-
61
-
-
0037059986
-
Lewis acid catalyzed acylation reactions: Scope and limitations
-
(d) Chandra, K.L.; Saravanan, P.; Singh, R.K.; Singh, V.K. Lewis acid catalyzed acylation reactions: scope and limitations. Tetrahedron Lett., 2002, 58, 1369-1374.
-
(2002)
Tetrahedron Lett.
, vol.58
, pp. 1369-1374
-
-
Chandra, K.L.1
Saravanan, P.2
Singh, R.K.3
Singh, V.K.4
-
62
-
-
0035796424
-
Bismuth (III) salts as convenient and efficient catalysts for the selective acetylation and benzoylation of alcohols and phenols
-
(e) Mohammadpoor-Baltork, I.; Aliyan, H.; Khosropour, A.R. Bismuth (III) salts as convenient and efficient catalysts for the selective acetylation and benzoylation of alcohols and phenols. Tetrahedron Lett., 2001, 57, 5851-5854.
-
(2001)
Tetrahedron Lett.
, vol.57
, pp. 5851-5854
-
-
Mohammadpoor-Baltork, I.1
Aliyan, H.2
Khosropour, A.R.3
-
63
-
-
2342646700
-
3
-
3. Green Chem., 2004, 6, 191-192.
-
(2004)
Green Chem.
, vol.6
, pp. 191-192
-
-
Bartoli, G.1
Dalpozzo, R.2
De Nino, A.3
Maiuolo, L.4
Nardi, M.5
Procopio, A.6
Tagarelli, A.7
-
65
-
-
38749099029
-
2O-catalyzed per-O-acetylation of sugars compatible with acid-labile protecting groups adopted in carbohydrate chemistry
-
2O-catalyzed per-O-acetylation of sugars compatible with acid-labile protecting groups adopted in carbohydrate chemistry. Tetrahedron Lett., 2008, 64, 2572-2575.
-
(2008)
Tetrahedron Lett.
, vol.64
, pp. 2572-2575
-
-
Shi, L.1
Zhang, G.2
Pan, F.3
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