-
1
-
-
0032482080
-
Modern variants of the Mannich reaction
-
doi: 10.1002/(SICI)1521-3773(19980504)37:8%3C;1044::AID-ANIE1044%3E;3.0. CO;2-E
-
Arend M, Westermann B, Risch N (1998) Modern variants of the Mannich reaction. Angew Chem Int Ed 37:1044-1070. doi: 10.1002/(SICI)1521-3773(19980504) 37:8%3C;1044::AID-ANIE1044%3E;3.0.CO;2-E
-
(1998)
Angew Chem Int Ed
, vol.37
, pp. 1044-1070
-
-
Arend, M.1
Westermann, B.2
Risch, N.3
-
2
-
-
0038796876
-
N,N-Phthaloylamino acids as chiral auxiliaries in asymmetric Mannich-type reactions
-
doi: 10.1002/(SICI)1521-3773(19990115)38:1/2%3C;184:AID-NIE184%3E;3.0. CO;2-E
-
Muller R, Goesmann N, Waldmann H (1999) N,N-Phthaloylamino acids as chiral auxiliaries in asymmetric Mannich-type reactions. Angew Chem Int Ed 38:184-187. doi: 10.1002/(SICI)1521-3773(19990115)38:1/2%3C;184:AID-NIE184%3E;3. 0.CO;2-E
-
(1999)
Angew Chem Int Ed
, vol.38
, pp. 184-187
-
-
Muller, R.1
Goesmann, N.2
Waldmann, H.3
-
3
-
-
0346456942
-
Microwave-assisted Mannich-type three-component reactions
-
doi: 10.1023/B:MODI.0000006822.51884.e6
-
Leadbeater NE, Torenius HM, Tye H (2003) Microwave-assisted Mannich-type three-component reactions. Mol Divers 7: 135-144. doi: 10.1023/B:MODI. 0000006822.51884.e6
-
(2003)
Mol Divers
, vol.7
, pp. 135-144
-
-
Leadbeater, N.E.1
Torenius, H.M.2
Tye, H.3
-
4
-
-
31044436897
-
Mannich reaction in Bronsted acidic ionic liquid: A facile synthesis of 2-amino carbonyl compounds
-
10.1016/j.molcata.2005.09.012 10.1016/j.molcata.2005.09.012 1:CAS:528:DC%2BD28XovVWrsg%3D%3D
-
Sahoo S, Joseph T, Halligudi SB (2006) Mannich reaction in Bronsted acidic ionic liquid: a facile synthesis of 2-amino carbonyl compounds. J Mol Catal A 244:179-182. doi: 10.1016/j.molcata.2005.09.012
-
(2006)
J Mol Catal A
, vol.244
, pp. 179-182
-
-
Sahoo, S.1
Joseph, T.2
Halligudi, S.B.3
-
5
-
-
84860390435
-
2 as a heterogeneous catalyst in an efficient one-pot three-component Mannich synthesis of β -aminocarbonyls
-
doi: 10.1016/j.cclet.2011.05.019
-
2 as a heterogeneous catalyst in an efficient one-pot three-component Mannich synthesis of β -aminocarbonyls. Chin Chem Lett 22:1203-1206. doi: 10.1016/j.cclet.2011.05.019
-
(2011)
Chin Chem Lett
, vol.22
, pp. 1203-1206
-
-
Kassaee, M.Z.1
Mohammadi, R.2
Masrouri, H.3
Movahedi, F.4
-
6
-
-
35448993521
-
Synthesis of β-amino carbonyl compounds via a Mannich reaction catalyzed by Salen-Zn complex
-
10.1016/j.catcom.2007.05.011 10.1016/j.catcom.2007.05.011 1:CAS:528:DC%2BD2sXht1GhtL7N
-
Wu M, Jing H, Chang T (2007) Synthesis of β-amino carbonyl compounds via a Mannich reaction catalyzed by Salen-Zn complex. Catal Commun 8:2217-2221. doi: 10.1016/j.catcom.2007.05.011
-
(2007)
Catal Commun
, vol.8
, pp. 2217-2221
-
-
Wu, M.1
Jing, H.2
Chang, T.3
-
7
-
-
50849109479
-
CAN catalyzed synthesis of β -amino carbonyl compounds via Mannich reaction in PEG
-
doi: 10.1016/j.catcom.2008.07.010
-
Kidwai M, Bhatnagar D, Mishra NK, Bansal V (2008) CAN catalyzed synthesis of β-amino carbonyl compounds via Mannich reaction in PEG. Catal Commun 9:2547-2549. doi: 10.1016/j.catcom.2008.07.010
-
(2008)
Catal Commun
, vol.9
, pp. 2547-2549
-
-
Kidwai, M.1
Bhatnagar, D.2
Mishra, N.K.3
Bansal, V.4
-
8
-
-
70350010182
-
Bismuth(III) chloride-catalyzed one-pot Mannich reaction: Three-component synthesis of β-amino carbonyl compounds
-
doi: 10.1016/j.tetlet.2009.09.131
-
Li H, Zeng H, Shao H (2009) Bismuth(III) chloride-catalyzed one-pot Mannich reaction: three-component synthesis of β-amino carbonyl compounds. Tetrahedron Lett 50:6858-6860. doi: 10.1016/j.tetlet.2009.09.131
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 6858-6860
-
-
Li, H.1
Zeng, H.2
Shao, H.3
-
9
-
-
10844226557
-
Bismuth triflate-catalyzed three-component Mannich-type reaction
-
10.1021/jo048617c 15609969 10.1021/jo048617c 1:CAS:528: DC%2BD2cXpslyksbs%3D
-
Ollevier T, Nadeau E (2004) Bismuth triflate-catalyzed three-component Mannich-type reaction. J Org Chem 69:9292-9295. doi: 10.1021/jo048617c
-
(2004)
J Org Chem
, vol.69
, pp. 9292-9295
-
-
Ollevier, T.1
Nadeau, E.2
-
10
-
-
33750867909
-
Mannich-type reactions of aromatic aldehydes, anilines, and methyl ketones in fluorous biphase systems created by rare earth (III) perfluorooctane sulfonates catalysts in fluorous media
-
10.1016/j.jfluchem.2006.07.009 10.1016/j.jfluchem.2006.07.009
-
Yi W, Cai C (2006) Mannich-type reactions of aromatic aldehydes, anilines, and methyl ketones in fluorous biphase systems created by rare earth (III) perfluorooctane sulfonates catalysts in fluorous media. J Fluorine Chem 12:1515-1521. doi: 10.1016/j.jfluchem.2006.07.009
-
(2006)
J Fluorine Chem
, vol.12
, pp. 1515-1521
-
-
Yi, W.1
Cai, C.2
-
12
-
-
33744758029
-
Highly efficient one-pot three-component Mannich reaction in water catalyzed by heteropoly acids
-
10.1021/ol060498v 16671786 10.1021/ol060498v 1:CAS:528: DC%2BD28XjsFOitbo%3D
-
Azizi N, Torkiyan L, Saidi MR (2006) Highly efficient one-pot three-component Mannich reaction in water catalyzed by heteropoly acids. Org Lett 8:2079-2082. doi: 10.1021/ol060498v
-
(2006)
Org Lett
, vol.8
, pp. 2079-2082
-
-
Azizi, N.1
Torkiyan, L.2
Saidi, M.R.3
-
13
-
-
67649114374
-
Lipase-catalysed direct Mannich reaction in water: Utilization of biocatalytic promiscuity for C-C bond formation in a "one-pot" synthesis
-
10.1039/B817524A 10.1039/b817524a 1:CAS:528:DC%2BD1MXmvV2qtrc%3D
-
Li K, He T, Li C, Feng X-W, Wang N, Yu X-Q (2009) Lipase-catalysed direct Mannich reaction in water: utilization of biocatalytic promiscuity for C-C bond formation in a "one-pot" synthesis. Green Chem 11:777-779. doi: 10.1039/B817524A
-
(2009)
Green Chem
, vol.11
, pp. 777-779
-
-
Li, K.1
He, T.2
Li, C.3
Feng, X.-W.4
Wang, N.5
Yu, X.-Q.6
-
14
-
-
33748702885
-
Total synthesis of ent-sedridine using proline-catalyzed asymmetric-addition as a key step
-
10.1055/s-2006-948203 10.1055/s-2006-948203
-
Itoh T, Nishimura K, Nagata K, Yokoya M (2006) Total synthesis of ent-sedridine using proline-catalyzed asymmetric-addition as a key step. Synlett 14:2207-2210. doi: 10.1055/s-2006-948203
-
(2006)
Synlett
, vol.14
, pp. 2207-2210
-
-
Itoh, T.1
Nishimura, K.2
Nagata, K.3
Yokoya, M.4
-
15
-
-
33846550172
-
Proline-catalyzed Mannich reaction of aldehydes with N-boc-imines
-
doi: 10.1002/anie.200603188
-
Yang JW, Stadler M, List B (2007) Proline-catalyzed Mannich reaction of aldehydes with N-boc-imines. Angew Chem Int Ed 46: 609-611. doi: 10.1002/anie.200603188
-
(2007)
Angew Chem Int Ed
, vol.46
, pp. 609-611
-
-
Yang, J.W.1
Stadler, M.2
List, B.3
-
16
-
-
34548384384
-
Highly efficient AILs/L -proline synergistic catalyzed three-component asymmetric Mannich reaction
-
10.1080/00397910601163976 10.1080/00397910601163976 1:CAS:528: DC%2BD2sXpvVKqsb8%3D
-
Liu BY, Xu DQ, Dong JF, Yang HL, Zhao DS, Luo SP, Xu ZY (2007) Highly efficient AILs/L -proline synergistic catalyzed three-component asymmetric Mannich reaction. Synth Commun 37:3003-3010. doi: 10.1080/00397910601163976
-
(2007)
Synth Commun
, vol.37
, pp. 3003-3010
-
-
Liu, B.Y.1
Xu, D.Q.2
Dong, J.F.3
Yang, H.L.4
Zhao, D.S.5
Luo, S.P.6
Xu, Z.Y.7
-
17
-
-
38749144743
-
Direct asymmetric three-component Mannich reactions catalyzed by a siloxy serine organocatalyst in water
-
0.1016/j.tetasy.2007.12.011 10.1016/j.tetasy.2007.12.011 1:CAS:528:DC%2BD1cXhsFahsb4%3D
-
Teo MC, Lau JJ, Wu MC (2008) Direct asymmetric three-component Mannich reactions catalyzed by a siloxy serine organocatalyst in water. Tetrahedron 19:186-190. doi: 0.1016/j.tetasy.2007.12.011
-
(2008)
Tetrahedron
, vol.19
, pp. 186-190
-
-
Teo, M.C.1
Lau, J.J.2
Wu, M.C.3
-
18
-
-
79960950478
-
An efficient non-ionic surfactant catalyzed multicomponent synthesis of novel benzylamino coumarin derivative via Mannich type reaction in aqueous media
-
10.1016/j.tetlet.2011.06.040 10.1016/j.tetlet.2011.06.040 1:CAS:528:DC%2BC3MXps1Wgtrk%3D
-
Kumar A, Gupta MK, Kumar M (2011) An efficient non-ionic surfactant catalyzed multicomponent synthesis of novel benzylamino coumarin derivative via Mannich type reaction in aqueous media. Tetrahedron Lett 52:4521-4525. doi: 10.1016/j.tetlet.2011.06.040
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 4521-4525
-
-
Kumar, A.1
Gupta, M.K.2
Kumar, M.3
-
19
-
-
84455161188
-
Highly efficient one-pot three-component Mannich reaction catalyzed by ZnO-nanoparticles in water
-
MaGee DI, Dabiri M, Salehi P, Torkian L (2011) Highly efficient one-pot three-component Mannich reaction catalyzed by ZnO-nanoparticles in water. Arkivoc 11:156-164
-
(2011)
Arkivoc
, vol.11
, pp. 156-164
-
-
Magee, D.I.1
Dabiri, M.2
Salehi, P.3
Torkian, L.4
-
20
-
-
78649603139
-
2O) as a highly efficient catalyst for one-pot three-component Mannich reaction
-
10.1590/S0103-50532010001200002 1:CAS:528:DC%2BC3MXhtlCnu78%3D
-
2O) as a highly efficient catalyst for one-pot three-component Mannich reaction. J Braz Chem Soc 21:2175-2179
-
(2010)
J Braz Chem Soc
, vol.21
, pp. 2175-2179
-
-
Kidwai, M.1
Jahan, A.2
-
22
-
-
33745621606
-
Phenylboronic acid as a mild and efficient catalyst for Biginelli reaction
-
doi: 10.1016/j.tetlet.2006.06.015
-
Dabache A, Boumoud B, Amimour M, Belfaitah A, Rhouati S, Carboni B (2006) Phenylboronic acid as a mild and efficient catalyst for Biginelli reaction. Tetrahedron Lett 47:5697-5699. doi: 10.1016/j.tetlet.2006.06.015
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 5697-5699
-
-
Dabache, A.1
Boumoud, B.2
Amimour, M.3
Belfaitah, A.4
Rhouati, S.5
Carboni, B.6
-
23
-
-
79960286560
-
Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives
-
doi: 10.1016/j.tetlet.2011.06.039
-
Lopez-Ruiz H, Briseno-Ortega H, Rojas-Lima S, Santillan R, Farfan N (2011) Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives. Tetrahedron Lett 52:4308-4312. doi: 10.1016/j.tetlet.2011.06.039
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 4308-4312
-
-
Lopez-Ruiz, H.1
Briseno-Ortega, H.2
Rojas-Lima, S.3
Santillan, R.4
Farfan, N.5
-
24
-
-
33747879769
-
A novel 3-nitrobenzeneboronic acid as an extremely mild and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions
-
10.1016/j.tetlet.2006.07.046 10.1016/j.tetlet.2006.07.046 1:CAS:528:DC%2BD28XptVCisrg%3D
-
Tale RH, Adude RN (2006) A novel 3-nitrobenzeneboronic acid as an extremely mild and environmentally benign catalyst for the acetylation of alcohols under solvent-free conditions. Tetrahedron Lett 47:7263-7265. doi: 10.1016/j.tetlet.2006.07.046
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 7263-7265
-
-
Tale, R.H.1
Adude, R.N.2
-
25
-
-
77954244056
-
Mild and efficient boronic acid catalysis of Diels-Alder cycloadditions to 2-alkynoic acids
-
10.1016/j.tetlet.2010.04.132 10.1016/j.tetlet.2010.04.132 1:CAS:528:DC%2BC3cXntVygtrc%3D
-
Zheng H, Hall DG (2010) Mild and efficient boronic acid catalysis of Diels-Alder cycloadditions to 2-alkynoic acids. Tetrahedron Lett 51:3561-3564. doi: 10.1016/j.tetlet.2010.04.132
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 3561-3564
-
-
Zheng, H.1
Hall, D.G.2
-
26
-
-
75749112059
-
Boronic acid catalyzed Friedel-Crafts reactions of allylic alcohols with electron-rich arenes and heteroarenes
-
doi: 10.1021/jo9023073
-
McCubbin JA, Hosseini H, Krokhin OV (2010) Boronic acid catalyzed Friedel-Crafts reactions of allylic alcohols with electron-rich arenes and heteroarenes. J Org Chem 75:959-962. doi: 10.1021/jo9023073
-
(2010)
J Org Chem
, vol.75
, pp. 959-962
-
-
McCubbin, J.A.1
Hosseini, H.2
Krokhin, O.V.3
-
27
-
-
79959486571
-
Mild and selective boronic acid catalyzed 1,3-transposition of allylic alcohols and Meyer-Schuster rearrangement of propargylic alcohols
-
doi: 10.1039/c1sc00140j
-
Zheng H, Lejkowski M, Hall DG (2011) Mild and selective boronic acid catalyzed 1,3-transposition of allylic alcohols and Meyer-Schuster rearrangement of propargylic alcohols. Chem Sci 2: 1305-1310. doi: 10.1039/c1sc00140j
-
(2011)
Chem Sci
, vol.2
, pp. 1305-1310
-
-
Zheng, H.1
Lejkowski, M.2
Hall, D.G.3
-
28
-
-
41049106516
-
One-pot synthesis of 1,4-dihydropyridines via a phenylboronic acid catalyzed Hantztch three-component reaction
-
10.1055/s-2008-1032093 10.1055/s-2008-1032093
-
Dabache A, Boulcina R, Belfaitah A, Rhouati S, Carboni B (2008) One-pot synthesis of 1,4-dihydropyridines via a phenylboronic acid catalyzed Hantztch three-component reaction. Synlett 4:509-512. doi: 10.1055/s-2008-1032093
-
(2008)
Synlett
, vol.4
, pp. 509-512
-
-
Dabache, A.1
Boulcina, R.2
Belfaitah, A.3
Rhouati, S.4
Carboni, B.5
-
29
-
-
33344467684
-
3-Nitrobenzeneboronic acid as an efficient and environmentally benign catalyst for the selective transesterfication of β-keto esters
-
doi: 10.1055/s-2006-932454
-
Tale RH, Sagar AD, Santan HD, Adude RN (2006) 3-Nitrobenzeneboronic acid as an efficient and environmentally benign catalyst for the selective transesterfication of β -keto esters. Synlett 3:415-418. doi: 10.1055/s-2006-932454
-
(2006)
Synlett
, vol.3
, pp. 415-418
-
-
Tale, R.H.1
Sagar, A.D.2
Santan, H.D.3
Adude, R.N.4
-
30
-
-
84864115931
-
Phenylboronic acid as efficient and eco-friendly catalyst for the one-pot, three-component synthesis of β-aminophosphonates under solvent-free conditions
-
doi: 10.1055/s-0032-1316558
-
Tibhe GD, Bedolla-Medrano M, Cativiela C, Ordonez M (2012) Phenylboronic acid as efficient and eco-friendly catalyst for the one-pot, three-component synthesis of β-aminophosphonates under solvent-free conditions. Synlett 23:1931-1936. doi: 10.1055/s-0032-1316558
-
(2012)
Synlett
, vol.23
, pp. 1931-1936
-
-
Tibhe, G.D.1
Bedolla-Medrano, M.2
Cativiela, C.3
Ordonez, M.4
-
31
-
-
13644253035
-
A new protocol to synthesize 1,4-dihydropyridines by using 3,4,5-Trifluorobenzeneboronic acid as a catalyst in ionic liquid: Synthesis of novel 4-(3-carboxyl-1H-pyrazol-4-yl)-1,4-dihydropyridines
-
10.1016/j.tet.2005.01.008 10.1016/j.tet.2005.01.008 1:CAS:528: DC%2BD2MXhtlSktbY%3D
-
Sridhar R, Perumal PT (2005) A new protocol to synthesize 1,4-dihydropyridines by using 3,4,5-Trifluorobenzeneboronic acid as a catalyst in ionic liquid: synthesis of novel 4-(3-carboxyl-1H-pyrazol-4-yl)-1,4- dihydropyridines. Tetrahedron 61:2465-2470. doi: 10.1016/j.tet.2005.01.008
-
(2005)
Tetrahedron
, vol.61
, pp. 2465-2470
-
-
Sridhar, R.1
Perumal, P.T.2
-
32
-
-
84868605928
-
3-Nitrophenylboronic acid-catalyzed efficient one-pot synthesis of 1,4-dihydropyridines and polyhydroquinolines
-
10.1186/2228-5547-3-6 10.1186/2228-5547-3-6
-
Adude RN, Tigote RM, Goswami SV, Bhusare SR (2012) 3-Nitrophenylboronic acid-catalyzed efficient one-pot synthesis of 1,4-dihydropyridines and polyhydroquinolines. Int J Ind Chem 3:6. doi: 10.1186/2228-5547-3-6
-
(2012)
Int J Ind Chem
, vol.3
, pp. 6
-
-
Adude, R.N.1
Tigote, R.M.2
Goswami, S.V.3
Bhusare, S.R.4
-
33
-
-
80053525233
-
Phenylboronic acid-catalyzed synthesis of 9,9-dimethyl-12-phenyl-9,10- dihydro-8h-benzo[a]xanthen-11(12h)-one derivatives
-
1:CAS:528:DC%2BC3MXhsVGltbzP
-
Goswami SV, Thorat PB, Dhone SS, Bhusare SR (2011) Phenylboronic acid-catalyzed synthesis of 9,9-dimethyl-12-phenyl-9,10-dihydro-8h-benzo[a] xanthen-11(12h)-one derivatives. J Chem Pharm Res 3(5):632-635
-
(2011)
J Chem Pharm Res
, vol.3
, Issue.5
, pp. 632-635
-
-
Goswami, S.V.1
Thorat, P.B.2
Dhone, S.S.3
Bhusare, S.R.4
|