-
1
-
-
0346116581
-
-
Wiley-VCH: Weinheim, Germany
-
(a) Otera, J. Esterification; Wiley-VCH: Weinheim, Germany, 2003.
-
(2003)
Esterification
-
-
Otera, J.1
-
2
-
-
0001595852
-
Transesterification
-
(b) Otera, J. Transesterification. Chem. Rev. 1993, 93, 1449-1470.
-
(1993)
Chem. Rev.
, vol.93
, pp. 1449-1470
-
-
Otera, J.1
-
3
-
-
0026418434
-
The atom economy-a search for synthetic efficiency
-
(a) Trost, B. A. The atom economy-a search for synthetic efficiency. Science 1991, 254, 1471-1477.
-
(1991)
Science
, vol.254
, pp. 1471-1477
-
-
Trost, B.A.1
-
4
-
-
0347933770
-
Catalysis and pollution prevention
-
(b) Sheldon, R. A. Catalysis and pollution prevention. Chem. Ind. (London) 1997, 12-15.
-
(1997)
Chem. Ind. (London)
, pp. 12-15
-
-
Sheldon, R.A.1
-
5
-
-
0001236731
-
In search of practical esterification
-
Otera, J. In search of practical esterification. Angew. Chem., Int. Ed. 2001, 40, 2044-2045.
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 2044-2045
-
-
Otera, J.1
-
6
-
-
33847804947
-
Graphite electrolytic lamellar reagents in organic chemistry. Esterifications in the presence of graphite bisulfate
-
Olah, G. A.; Liand, G.; Staral, J. Graphite electrolytic lamellar reagents in organic chemistry. Esterifications in the presence of graphite bisulfate. J. Am. Chem. Soc. 1974, 96, 8113-8115.
-
(1974)
J. Am. Chem. Soc.
, vol.96
, pp. 8113-8115
-
-
Olah, G.A.1
Liand, G.2
Staral, J.3
-
7
-
-
0032874630
-
Catalytic esterifications of carboxylic acids and alcohols by sodium bisulfate monohydrate
-
Li, Y.-Q. Catalytic esterifications of carboxylic acids and alcohols by sodium bisulfate monohydrate. Synth. Commun. 1999, 3901-3903.
-
(1999)
Synth. Commun.
, pp. 3901-3903
-
-
Li, Y.-Q.1
-
8
-
-
0034634399
-
Direct condensation of carboxylic acids with alcohols catalyzed by hafnium (IV) salts
-
(a) Ishihara, K.; Ohara, S.; Yamamoto, H. Direct condensation of carboxylic acids with alcohols catalyzed by hafnium (IV) salts. Science 2000, 290, 1140-1142.
-
(2000)
Science
, vol.290
, pp. 1140-1142
-
-
Ishihara, K.1
Ohara, S.2
Yamamoto, H.3
-
9
-
-
0037037934
-
Direct ester condensation from a 1:1 mixture of carboxylic acids and alcohols catalyzed by hafnium (IV) and zirconium (IV) salts
-
(b) Ishihara, K.; Nakayama, M.; Ohara, S.; Yamamoto, H. Direct ester condensation from a 1:1 mixture of carboxylic acids and alcohols catalyzed by hafnium (IV) and zirconium (IV) salts. Tetrahedron 2002, 58, 8179-8188.
-
(2002)
Tetrahedron
, vol.58
, pp. 8179-8188
-
-
Ishihara, K.1
Nakayama, M.2
Ohara, S.3
Yamamoto, H.4
-
10
-
-
0034234818
-
Diphenylammonium triflate (DPAT): Efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols
-
Wakasugi, K.; Misaki, T.; Yamamda, K.; Tanabe, Y. Diphenylammonium triflate (DPAT): efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols. Tetrahedron Lett. 2000, 41, 5249-5252.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 5249-5252
-
-
Wakasugi, K.1
Misaki, T.2
Yamamda, K.3
Tanabe, Y.4
-
11
-
-
0037048606
-
Dehydration reaction in water. Brønsted acid-surfactant-combined catalyst for ester, ether, thioether, and dithioacetal formation in water
-
Manabe, K.; Iimura, S.; Sun, X.-M.; Kobayashi, S. Dehydration reaction in water. Brønsted acid-surfactant-combined catalyst for ester, ether, thioether, and dithioacetal formation in water. J. Am. Chem. Soc. 2002, 124, 11971-11978.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 11971-11978
-
-
Manabe, K.1
Iimura, S.2
Sun, X.-M.3
Kobayashi, S.4
-
12
-
-
0002694574
-
A facile and selective synthesis of β-keto esters via zeolite catalyzed transesterification
-
(a) Balaji, B. S.; Sasidharan, M.; Kumar, R.; Chanda, B. A facile and selective synthesis of β-keto esters via zeolite catalyzed transesterification. Chem. Commun. 1996, 707-708.
-
(1996)
Chem. Commun.
, pp. 707-708
-
-
Balaji, B.S.1
Sasidharan, M.2
Kumar, R.3
Chanda, B.4
-
13
-
-
0343049165
-
A facile and selective procedure for transesterification of β-keto esters promoted by Yttria-Zirconia based Lewis acid catalyst
-
(b) Kumar, P.; Pandey, R. K. A facile and selective procedure for transesterification of β-keto esters promoted by Yttria-Zirconia based Lewis acid catalyst. Synlett 2000, 251-253.
-
(2000)
Synlett.
, pp. 251-253
-
-
Kumar, P.1
Pandey, R.K.2
-
14
-
-
0034748995
-
Chemoselective transesterification of β-keto esters under neutral conditions using NBS as a catalyst
-
(c) Bandgar, B. P.; Uppalla, V. S.; Sadavarte, V. S. Chemoselective transesterification of β-keto esters under neutral conditions using NBS as a catalyst. Synlett 2001, 1715-1718.
-
(2001)
Synlett
, pp. 1715-1718
-
-
Bandgar, B.P.1
Uppalla, V.S.2
Sadavarte, V.S.3
-
15
-
-
0038372081
-
Flourous biphase chemistry
-
(a) Horváth, I. T. Flourous Biphase Chemistry. Acc. Chem. Res. 1998, 31, 641-650.
-
(1998)
Acc. Chem. Res.
, vol.31
, pp. 641-650
-
-
Horváth, I.T.1
-
16
-
-
0028116494
-
Are Teflon "ponytails" the coming fashion for catalysis?
-
(b) Gladysz, J. A. Are Teflon "ponytails" the coming fashion for catalysis? Science 1994, 266, 55-56.
-
(1994)
Science
, vol.266
, pp. 55-56
-
-
Gladysz, J.A.1
-
17
-
-
0345982287
-
Flourous biphase catalysis
-
(c) Hope, E. G.; Stuart, A. M. Flourous biphase catalysis. J. Fluorine Chem. 1999, 100, 75-83.
-
(1999)
J. Fluorine Chem.
, vol.100
, pp. 75-83
-
-
Hope, E.G.1
Stuart, A.M.2
-
18
-
-
57249105053
-
Fluorous techniques for the synthesis and separation of organic molecules
-
(d) Curran, D.; Lee, Z. Fluorous techniques for the synthesis and separation of organic molecules. Green Chem. 2003, G3-G7.
-
(2003)
Green Chem.
-
-
Curran, D.1
Lee, Z.2
-
19
-
-
0001258988
-
Template effects of distannoxanes
-
Coxon, J. M., Ed.; JAI Press Inc.: Greenwich, CT
-
Otera, J. Template effects of distannoxanes. In Advances in Detailed Reaction Mechanisms; Coxon, J. M., Ed.; JAI Press Inc.: Greenwich, CT, 1994; Vol. 3, pp 167-197.
-
(1994)
Advances in Detailed Reaction Mechanisms
, vol.3
, pp. 167-197
-
-
Otera, J.1
-
20
-
-
33751500481
-
Novel template effects of distannoxane catalysts in highly efficient transesterfication and esterification
-
Otera, J.; Dan-oh, N.; Nozaki, H. Novel template effects of distannoxane catalysts in highly efficient transesterfication and esterification. J. Org. Chem. 1991, 56, 5307-5311.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 5307-5311
-
-
Otera, J.1
Dan-Oh, N.2
Nozaki, H.3
-
21
-
-
0023809116
-
Total synthesis of (±)-myrocin C
-
For example: (a) Schreiber, S. L.; Meyers, H. V. Total Synthesis of (±)-Myrocin C. J. Am. Chem. Soc. 1988, 110, 5198-5200.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 5198-5200
-
-
Schreiber, S.L.1
Meyers, H.V.2
-
22
-
-
0024268946
-
On the use of unsymmetrically substituted furans in the furan-carbonyl photo-cycloaddition reaction: Synthesis of a kadsurenone-ginkgolide hybrid
-
(b) Schreiber, S. L.; Desmaele, D.; Porco, J. A., Jr. On the use of unsymmetrically substituted furans in the furan-carbonyl photo-cycloaddition reaction: synthesis of a kadsurenone-ginkgolide hybrid. Tetrahedron Lett. 1988, 29, 6689-6692.
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 6689-6692
-
-
Schreiber, S.L.1
Desmaele, D.2
Porco Jr., J.A.3
-
23
-
-
0011879781
-
Chiral synthesis of (-)-colletol based on palladium-catalyzed reductive cleavage of alkenyloxiranes with formic acid
-
(c) Shimizu, I.; Omura, T. Chiral synthesis of (-)-colletol based on palladium-catalyzed reductive cleavage of alkenyloxiranes with formic acid. Chem. Lett. 1993, 1759-1760.
-
(1993)
Chem. Lett.
, pp. 1759-1760
-
-
Shimizu, I.1
Omura, T.2
-
24
-
-
0032879750
-
Synthesis and preliminary evaluation of a library of polycyclic small molecules for use in chemical genetic assays
-
(d) Tan, D. S.; Foley, M. A.; Srockwell, B. R.; Shair, M. D.; Schreiber, S. L. Synthesis and preliminary evaluation of a library of polycyclic small molecules for use in chemical genetic assays. J. Am. Chem. Soc. 1999, 121, 9073-9087.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 9073-9087
-
-
Tan, D.S.1
Foley, M.A.2
Srockwell, B.R.3
Shair, M.D.4
Schreiber, S.L.5
-
25
-
-
0005169912
-
A novel template effect of distannoxane in macrolactonization of ω-hydroxy carboxylic acids
-
Otera, J.; Yano, T.; Himeno, Y.; Nozaki, H. A novel template effect of distannoxane in macrolactonization of ω-hydroxy carboxylic acids. Tetrahedron Lett. 1986, 27, 4501-4504.
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 4501-4504
-
-
Otera, J.1
Yano, T.2
Himeno, Y.3
Nozaki, H.4
-
26
-
-
0020858731
-
Tin-mediated esterification in macrolide synthesis
-
Steliou, K.; Poupart, M.-A. Tin-mediated esterification in Macrolide Synthesis. J. Am. Chem. Soc. 1983, 105, 7130-7138.
-
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 7130-7138
-
-
Steliou, K.1
Poupart, M.-A.2
-
27
-
-
0036533277
-
Synthesis and characterization of fluoroalkyldistannoxanes
-
Xiang, J.; Orita, A.; Otera, J. Synthesis and characterization of fluoroalkyldistannoxanes. J. Organomet. Chem. 2001, 648, 246-250.
-
(2001)
J. Organomet. Chem.
, vol.648
, pp. 246-250
-
-
Xiang, J.1
Orita, A.2
Otera, J.3
-
28
-
-
0141515243
-
Assessment of fluoroalkyltin compounds as fluorous Lewis acid catalysts
-
Imakura, Y.; Nishiguchi, S.; Orita, A.; Otera, J. Assessment of fluoroalkyltin compounds as fluorous Lewis acid catalysts. Appl. Organomet. Chem. 2003, 17, 795-799.
-
(2003)
Appl. Organomet. Chem.
, vol.17
, pp. 795-799
-
-
Imakura, Y.1
Nishiguchi, S.2
Orita, A.3
Otera, J.4
-
29
-
-
0034597990
-
Selective sulfonylation of 1,2-diols and derivatives catalyzed by a recoverable fluorous tin oxide
-
Bucher, B.; Curran, D. P. Selective sulfonylation of 1,2-diols and derivatives catalyzed by a recoverable fluorous tin oxide. Tetrahedron Lett. 2000, 41, 9617-9621.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 9617-9621
-
-
Bucher, B.1
Curran, D.P.2
-
30
-
-
0021672896
-
Synthesis, characterization and anti-tumour activity of bis(polyfluoroalkyl)-tin dihalides
-
De Clercq, L.; Wileem, R.; Gielen, M.; Atassi, G. Synthesis, characterization and anti-tumour activity of bis(polyfluoroalkyl)-tin dihalides. Bull. Soc. Chim. Belg. 1984, 93, 1089-1097.
-
(1984)
Bull. Soc. Chim. Belg.
, vol.93
, pp. 1089-1097
-
-
De Clercq, L.1
Wileem, R.2
Gielen, M.3
Atassi, G.4
-
31
-
-
0000760581
-
A simple method for the esterificaiton of carboxylic acids using chlorosilanes
-
Nakao, R.; Oka, K.; Fukumoto, T. A simple method for the esterificaiton of carboxylic acids using chlorosilanes. Bull. Chem. Soc. Jpn. 1981, 54, 1267-1268.
-
(1981)
Bull. Chem. Soc. Jpn.
, vol.54
, pp. 1267-1268
-
-
Nakao, R.1
Oka, K.2
Fukumoto, T.3
-
33
-
-
2542432961
-
-
For preparation of these compounds, see ref 17
-
For preparation of these compounds, see ref 17.
-
-
-
-
35
-
-
0033591868
-
Fluorous tin hydrides: A new family of reagents for use in radical reactions
-
(b) Curran, D. P.; Hadida, S.; Kim, S. Y.; Luo, Z. Y. Fluorous tin hydrides: A new family of reagents for use in radical reactions. J. Am. Chem. Soc. 1999, 121, 6607-6615.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 6607-6615
-
-
Curran, D.P.1
Hadida, S.2
Kim, S.Y.3
Luo, Z.Y.4
-
36
-
-
0035477535
-
A practical and green chemical process: Fluoroalkyldistannoxane-catalyzed biphasic transesterification
-
(a) Xiang, J.; Toyoshima, S.; Orita, A.; Otera, J. A practical and green chemical process: fluoroalkyldistannoxane-catalyzed biphasic transesterification. Angew. Chem., Int. Ed. 2001, 40, 3670-3672.
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 3670-3672
-
-
Xiang, J.1
Toyoshima, S.2
Orita, A.3
Otera, J.4
-
37
-
-
0002809305
-
Fluoroalkyldistannxane catalysis for transesterification in fluorous biphase technology
-
(b) Xiang, J.; Orita, A.; Otera, J. Fluoroalkyldistannxane catalysis for transesterification in fluorous biphase technology. Adv. Synth. Catal. 2002, 344, 84-90.
-
(2002)
Adv. Synth. Catal.
, vol.344
, pp. 84-90
-
-
Xiang, J.1
Orita, A.2
Otera, J.3
-
38
-
-
0001144457
-
Reactivity profile of 1,3-disubsituted tetraorganodistannoxanes assessed in urethane formation reaction
-
Otera, J.; Yano, T.; Okawara, R. Reactivity profile of 1,3-disubsituted tetraorganodistannoxanes assessed in urethane formation reaction. Organometallics, 1986, 5, 1167-1170.
-
(1986)
Organometallics
, vol.5
, pp. 1167-1170
-
-
Otera, J.1
Yano, T.2
Okawara, R.3
-
39
-
-
0037702942
-
Dichlorodistannoxane transesterification catalysts, pure Lewis acids
-
Recently, a similar mechanism was proposed for transesterification catalyzed by 1,3-dichlorotetrabutyldistannoxane: Jousseaume, B.; Laporte, C.; Rascle, M.-C.; Toupance, T. Dichlorodistannoxane transesterification catalysts, pure Lewis acids. Chem. Commun. 2003, 1428-1429.
-
(2003)
Chem. Commun.
, pp. 1428-1429
-
-
Jousseaume, B.1
Laporte, C.2
Rascle, M.-C.3
Toupance, T.4
-
40
-
-
0001377704
-
Rapid fluorous Stille coupling reactions conducted under microwave irradiation
-
For the use of fluorous catalysts or reagents in organic solvent, see: (a) Larhed, M.; Hoshino, M.; Hadida, S.; Curran, D. P.; Hallberg, A. Rapid fluorous Stille coupling reactions conducted under microwave irradiation. J. Org. Chem. 1997, 62, 5583-5587.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 5583-5587
-
-
Larhed, M.1
Hoshino, M.2
Hadida, S.3
Curran, D.P.4
Hallberg, A.5
-
41
-
-
0035929950
-
Fluorous catalysis without fluorous solvents: A friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid-phase separation
-
(b) Wende, M.; Meier, R.; Gladysz, J. A. Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid-phase separation. J. Am. Chem. Soc. 2001, 123, 11490-11491.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 11490-11491
-
-
Wende, M.1
Meier, R.2
Gladysz, J.A.3
-
42
-
-
0037955542
-
Fluorous catalysis under homogeneous conditions without fluorous solvents: A "greener" catalyst recycling protocol based upon temperature-dependent solubilities and liquid/solid phase separation
-
(c) Wende, M.; Gladysz, J. A. Fluorous Catalysis under Homogeneous Conditions without Fluorous Solvents: A "Greener" Catalyst Recycling Protocol Based upon Temperature-Dependent Solubilities and Liquid/Solid Phase Separation. J. Am. Chem. Soc. 2003, 125, 5861-5872.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5861-5872
-
-
Wende, M.1
Gladysz, J.A.2
-
43
-
-
0034847130
-
3,5-Bis(perfluoroudecyl)phenylboronic acid as an easily recyclable direct amide condensation catalyst
-
(d) Ishihara, K.; Kondo, S.; Yamamoto, H. 3,5-Bis(perfluoroudecyl)phenylboronic acid as an easily recyclable direct amide condensation catalyst. Synlett 2001, 1371-1374.
-
(2001)
Synlett
, pp. 1371-1374
-
-
Ishihara, K.1
Kondo, S.2
Yamamoto, H.3
-
44
-
-
0036330924
-
A fluorous super Brønsted acid catalyst: Application to fluorous catalysis without fluorous solvents
-
(e) Ishihara, K.; Hasegawa, A.; Yamamoto, H. A fluorous super Brønsted acid catalyst: application to fluorous catalysis without fluorous solvents. Synlett 2002, 1299-1301.
-
(2002)
Synlett.
, pp. 1299-1301
-
-
Ishihara, K.1
Hasegawa, A.2
Yamamoto, H.3
-
46
-
-
85047696476
-
Fluorous biphase catalysts without perfluorinated solvents: Application to Pd-mediated Suzuki and Sonogashira couplings
-
(g) Tzschucke, C.; Markert, C.; Glatz, H.; Bannwarth, W. Fluorous biphase catalysts without perfluorinated solvents: Application to Pd-mediated Suzuki and Sonogashira couplings. Angew. Chem., Int. Ed. 2002, 41, 4500-4503.
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 4500-4503
-
-
Tzschucke, C.1
Markert, C.2
Glatz, H.3
Bannwarth, W.4
-
47
-
-
85047699868
-
Fluorous biphasic esterification directed towards ultimate atom efficiency
-
Xiang, J.; Orita, A.; Otera, J. Fluorous biphasic esterification directed towards ultimate atom efficiency. Angew. Chem., Int. Ed. 2002, 41, 4117-4119.
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 4117-4119
-
-
Xiang, J.1
Orita, A.2
Otera, J.3
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