-
1
-
-
0001461985
-
A tertiary phosphine-catalyzed reaction of acrylic compounds with aldehydes
-
Morita, K.; Suzuki, Z.; Hirose, H. A Tertiary Phosphine-catalyzed Reaction of Acrylic Compounds with Aldehydes. Bull. Chem Soc. Jpn. 1968, 41, 2815-2815
-
(1968)
Bull. Chem Soc. Jpn
, vol.41
, pp. 2815-2815
-
-
Morita, K.1
Suzuki, Z.2
Hirose, H.3
-
4
-
-
0003744531
-
-
34174q]
-
Chem. Abstr. 1972, 77, 34174q
-
Chem. Abstr
, pp. 77
-
-
-
5
-
-
0000077082
-
A simple synthesis of 2-methyledene-3-aminopropanoates
-
Perlmutter, P.; Teo, C.C. A simple synthesis of 2-methyledene-3- aminopropanoates Tetrahedron Lett. 1984, 25, 5951-5952.
-
(1984)
Tetrahedron Lett
, vol.25
, pp. 5951-5952
-
-
Perlmutter, P.1
Teo, C.C.2
-
6
-
-
0035886887
-
Enantioselective organocatalysis
-
Dalko, P.I.; Moisan, L. Enantioselective Organocatalysis. Angew. Chem. Int. Ed. 2001, 40, 3726-3748.
-
(2001)
Angew. Chem. Int. Ed
, vol.40
, pp. 3726-3748
-
-
Dalko, P.I.1
Moisan, L.2
-
7
-
-
0037170944
-
Amino acids and peptides as asymmetric organocatalysts
-
Jarvo, E.R.; Miller, S.J. Amino acids and peptides as asymmetric organocatalysts. Tetrahedron 2002, 58, 2481-2495.
-
(2002)
Tetrahedron
, vol.58
, pp. 2481-2495
-
-
Jarvo, E.R.1
Miller, S.J.2
-
8
-
-
0141619399
-
Polymer-supported organic catalysts
-
Benaglia, M.; Puglisi, A.; Cozzi, F. Polymer-Supported Organic Catalysts. Chem. Rev. 2003, 103, 3401-3430.
-
(2003)
Chem. Rev
, vol.103
, pp. 3401-3430
-
-
Benaglia, M.1
Puglisi, A.2
Cozzi, F.3
-
10
-
-
6044269452
-
The golden age of organocatalysis
-
Dalko, P.I.; Moisan, L. In the Golden Age of Organocatalysis. Angew. Chem. Int. Ed. 2004, 43, 5138-5175.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5138-5175
-
-
Dalko, P.I.1
Moisan, L.2
-
11
-
-
15244343428
-
Asymmetric organocatalysis
-
Seayad, J.; List, B. Asymmetric Organocatalysis. Org. Biomol. Chem. 2005, 3, 719-724.
-
(2005)
Org. Biomol. Chem
, vol.3
, pp. 719-724
-
-
Seayad, J.1
List, B.2
-
12
-
-
33845220042
-
Cupreines and cupreidines: An emerging class of bifunctional cinchona organocatalysts
-
Marcelli, T.; vanMaarseveen, J.H.; Hiemstra, H. Cupreines and Cupreidines: An Emerging Class of Bifunctional Cinchona Organocatalysts. Angew. Chem. Int. Ed. 2006, 45, 7496-7504.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7496-7504
-
-
Marcelli, T.1
Vanmaarseveen, J.H.2
Hiemstra, H.3
-
13
-
-
0036846203
-
Lewis base effects in the baylis-hillman reaction of arenecarbaldehydes and n-aryliden-4-methylbenzenesolfonamides with a-β-unsaturated cyclic ketones
-
Shi, M.; Xu, Y.-M.; Zhao, G.-L.; Wu, X.-F. Lewis Base Effects in the Baylis-Hillman Reaction of Arenecarbaldehydes and N-Aryliden-4- methylbenzenesolfonamides with a-β-Unsaturated Cyclic Ketones. Eur. J. Org. Chem. 2002, 3666-3679.
-
(2002)
Eur. J. Org. Chem.
, pp. 3666-3679
-
-
Shi, M.1
Xu, Y.-M.2
Zhao, G.-L.3
Wu, X.-F.4
-
14
-
-
0036180348
-
Lewis base effects in the baylis-hillman reaction of imines with methyl vinyl ketone
-
Shi, M.; Xu, Y.-M. Lewis base effects in the Baylis-Hillman Reaction of imines with methyl vinyl ketone. Eur. J. Org. Chem. 2002, 4, 696-701.
-
(2002)
Eur. J. Org. Chem.
, vol.4
, pp. 696-701
-
-
Shi, M.1
Xu, Y.-M.2
-
15
-
-
0037423248
-
Correlation between pka and reactivity of quinuclidine-based catalysts in the baylis-hillman reaction: discovery of quinuclidine as optimum catalyst leading to substantial enhancement of scope
-
Aggarwal, V.K.; Emme, S.Y.; Fulford, S.Y. Correlation between pKa and reactivity of quinuclidine-based catalysts in the Baylis-Hillman Reaction: discovery of quinuclidine as optimum catalyst leading to substantial enhancement of scope. J. Org. Chem. 2003, 68, 692-700.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 692-700
-
-
Aggarwal, V.K.1
Emme, S.Y.2
Fulford, S.Y.3
-
16
-
-
0033592809
-
Superior amine catalysts for the baylis-hillman reaction: The use of dbu and its implications.
-
Aggarwal, V.K.; Mereu, A. Superior amine catalysts for the Baylis-Hillman reaction: the use of DBU and its implications. Chem. Commun. 1999, 2311-2312.
-
(1999)
Chem. Commun.
, pp. 2311-2312
-
-
Aggarwal, V.K.1
Mereu, A.2
-
17
-
-
0032514440
-
M.m. dmap-catalyzed hydroxymethylation of 2-cyclohexenone in aqueous medium through baylis-hillman reaction
-
Rezgui, F.; El Gaied, M.M. DMAP-catalyzed hydroxymethylation of 2-cyclohexenone in aqueous medium through Baylis-Hillman reaction. Tetrahedron Lett. 1998, 39, 5965-5966.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 5965-5966
-
-
Rezgui, F.1
El Gaied2
-
18
-
-
0037037978
-
Aqueous baylis-hillman reaction of cyclopent-2-enone using imidazole as catalyst
-
Luo, S.; Zhang, B.; He, J.; Janczuk, A.; Wang, P.G.; Cheng, J. Aqueous Baylis-Hillman reaction of cyclopent-2-enone using imidazole as catalyst. Tetrahedron Lett. 2002, 43, 7369-7371.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 7369-7371
-
-
Luo, S.1
Zhang, B.2
He, J.3
Janczuk, A.4
Wang, P.G.5
Cheng, J.6
-
19
-
-
0034740381
-
Development of catalysts for the baylis-hillman reaction: The application of tetramethylguanidine and attempts to use a supported analogue
-
Leadbeater, N.E.; Van der Pol, C. Development of catalysts for the Baylis-Hillman reaction: the application of tetramethylguanidine and attempts to use a supported analogue. J. Chem. Soc. Perkin Trans. 2001, 1, 2831-2835.
-
(2001)
J. Chem. Soc. Perkin Trans
, vol.1
, pp. 2831-2835
-
-
Leadbeater, N.E.1
Van Der Pol, C.2
-
20
-
-
34548722252
-
N-heterocyclic carbene catalyzed aza-morita-baylis-hillman reaction of cyclic enones with n-tosylarylimines
-
He, L.; Jian, T.-Y.; Ye, S. N-Heterocyclic Carbene Catalyzed aza-Morita-Baylis-Hillman Reaction of Cyclic Enones with N-Tosylarylimines. J. Org. Chem. 2007, 72, 7466-7468.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 7466-7468
-
-
He, L.1
Jian, T.-Y.2
Ye, S.3
-
21
-
-
51949115828
-
Chiral bifunctional n-heterocyclic carbenes: Synthesis and application in the aza-morita-baylis-hillman reaction
-
He, L.; Zhang, Y.-R.; Huang, X.-L.; Ye, S. Chiral Bifunctional N-Heterocyclic Carbenes: Synthesis and Application in the aza-Morita-Baylis- Hillman Reaction. Synthesis 2008, 2825-2829.
-
(2008)
Synthesis
, pp. 2825-2829
-
-
He, L.1
Zhang, Y.-R.2
Huang, X.-L.3
Ye, S.4
-
22
-
-
0012504134
-
Entstehung von p-ylid aus triphenylphosphin und acrylsäurederivaten
-
Oda, R.; Kawabata, T.; Tanimoto, S. Entstehung von P-Ylid aus Triphenylphosphin und Acrylsäurederivaten. Tetrahedron Lett. 1964, 5, 1653-1657.
-
(1964)
Tetrahedron Lett.
, vol.5
, pp. 1653-1657
-
-
Oda, R.1
Kawabata, T.2
Tanimoto, S.3
-
23
-
-
5144220014
-
For a recent review: Methot, j.l.; roush, w.r. nucleophilic phosphine organocatalysis.
-
For a recent review: Methot, J.L.; Roush, W.R. Nucleophilic phosphine organocatalysis. Adv. Synth. Catal. 2004, 346, 1035-1050.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 1035-1050
-
-
-
24
-
-
50249134990
-
Lewis base catalysis in organic synthesis
-
Denmark, S.E.; Gregory, L.B. Lewis Base Catalysis in Organic Synthesis. Angew. Chem. Int. Ed. 2008, 47, 1560-1638.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 1560-1638
-
-
Denmark, S.E.1
Gregory, L.B.2
-
25
-
-
4744362831
-
Synthetic potential of the tertiary-amine-catalyzed reaction of activated vinyl carbanions with aldehydes
-
Drewes, S.E.; Roos, G.H.P. Synthetic potential of the tertiary-amine-catalyzed reaction of activated vinyl carbanions with aldehydes. Tetrahedron 1988, 44, 4653-4670.
-
(1988)
Tetrahedron
, vol.44
, pp. 4653-4670
-
-
Drewes, S.E.1
Roos, G.H.P.2
-
26
-
-
0342419508
-
The baylis-hillman reaction: A novel carbon-carbon forming reaction
-
Basavaiah, P.D. Rao; Hyma, R.S. The Baylis-Hillman reaction: a novel carbon-carbon forming reaction. Tetrahedron 1996, 52, 8001-8062.
-
(1996)
Tetrahedron
, vol.52
, pp. 8001-8062
-
-
Basavaiah, P.D.R.1
Hyma, R.S.2
-
27
-
-
0000892247
-
-
John Wiley & sons, Inc.: New York, NY, USA
-
Ciganek, E. Organic Reactions; John Wiley & sons, Inc.: New York, NY, USA, 1997; Volume 51, p. 201.
-
(1997)
Organic Reactions
, vol.51
, pp. 201
-
-
Ciganek, E.1
-
28
-
-
0034283585
-
New strategies for the development of an asymmetric version of the baylis-hillman reaction
-
Langer, P. New strategies for the development of an asymmetric version of the Baylis-Hillman reaction. Angew. Chem. Int. Ed. 2000, 39, 3049-3052.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 3049-3052
-
-
Langer, P.1
-
29
-
-
0037366617
-
Recent advances in the baylis-hillman reaction and applications
-
Basavaiah, D.; Rao, A.J. Satyanarayana, T.T. Recent advances in the Baylis-Hillman Reaction and Applications. Chem. Rev. 2003, 103, 811-892.
-
(2003)
Chem. Rev.
, vol.103
, pp. 811-892
-
-
Basavaiah, D.1
Rao, A.J.2
Satyanarayana, T.T.3
-
30
-
-
34548185871
-
The baylis-hillman reaction: A novel source of attraction, opportunities, and challenges in synthetic chemistry
-
Basavaiah, D.; Rao, K.V.; Reddy, R.J. The Baylis-Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry. Chem. Soc. Rev. 2007, 36, 1581-1588.
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 1581-1588
-
-
Basavaiah, D.1
Rao, K.V.2
Reddy, R.J.3
-
31
-
-
41649086484
-
Advances in the baylis-hillman reaction-assisted synthesis of cyclic frameworks
-
Singh, V.; Batra, S. Advances in the Baylis-Hillman reaction-assisted synthesis of cyclic frameworks. Tetrahedron 2008, 64, 4511-4574.
-
(2008)
Tetrahedron
, vol.64
, pp. 4511-4574
-
-
Singh, V.1
Batra, S.2
-
32
-
-
0037126262
-
Intramolecular baylis-hillman and morita reactions using unsaturated thiol ester substrates containing enolizable aldehydes
-
Keck, G.E.; Welch, D.S. Intramolecular Baylis-Hillman and Morita Reactions Using Unsaturated Thiol Ester Substrates Containing Enolizable Aldehydes. Org. Lett. 2002, 4, 3687-3690.
-
(2002)
Org. Lett.
, vol.4
, pp. 3687-3690
-
-
Keck, G.E.1
Welch, D.S.2
-
33
-
-
0001564208
-
4NX Combinations
-
Yagi, K.; Turitani, T.; Shinokubo, H.; Oshima, K. Intramolecular Tamdem Michael-Type Addition/Aldol Cyclization Induced by TiCl4/R4NX Combinations. Org. Lett. 2002, 4, 3111-3114.
-
(2002)
Org. Lett.
, vol.4
, pp. 3111-3114
-
-
Yagi, K.1
Turitani, T.2
Shinokubo, H.3
Oshima, K.4
-
34
-
-
34347355605
-
Aza-baylis-hillman reactions and their synthetic applications
-
Shi, Y.-L.; Shi, M. Aza-Baylis-Hillman reactions and their synthetic applications. Eur. J. Org. Chem. 2007, 2905-2916.
-
(2007)
Eur. J. Org. Chem.
, pp. 2905-2916
-
-
Shi, Y.-L.1
Shi, M.2
-
35
-
-
34347262098
-
The enantioselective morita-baylis-hillman reaction and its aza counterpart
-
Masson, G.; Housseman, C.; Zhu, J. The enantioselective Morita-Baylis-Hillman reaction and its aza counterpart. Angew. Chem. Int. Ed. 2007, 46, 4614-4628.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 4614-4628
-
-
Masson, G.1
Housseman, C.2
Zhu, J.3
-
36
-
-
59649098742
-
Aza-baylis-hillman reaction
-
Declerck, V.; Martinez, J.; Lamaty, F. Aza-Baylis-Hillman Reaction. Chem. Rev. 2009, 109, 1-48.
-
(2009)
Chem. Rev.
, vol.109
, pp. 1-48
-
-
Declerck, V.1
Martinez, J.2
Lamaty, F.3
-
37
-
-
70349280084
-
Recent extensions of the morita-baylis-hillman reaction
-
Ma, G.-N.; Jiang, J.-J.; Shi, M.; Wei, Y. Recent extensions of the Morita-Baylis-Hillman reaction. Chem. Commun. 2009, 5496-5514.
-
(2009)
Chem. Commun.
, pp. 5496-5514
-
-
Ma, G.-N.1
Jiang, J.-J.2
Shi, M.3
Wei, Y.4
-
38
-
-
84986992495
-
Mechanism of substitution reactions of acrylic derivatives
-
Hill, J.S.; Isaacs, N.S. Mechanism of substitution reactions of acrylic derivatives. J. Phys. Org. Chem. 1990, 3, 285-288.
-
(1990)
J. Phys. Org. Chem.
, vol.3
, pp. 285-288
-
-
Hill, J.S.1
Isaacs, N.S.2
-
40
-
-
84985521717
-
A new, efficient and stereocontrolled synthesis of trisubstituted alkenes via functionalized acrylic esters
-
Hoffman, H.R.M.; Rabe, J. A new, efficient and stereocontrolled synthesis of trisubstituted alkenes via functionalized acrylic esters. Angew. Chem. Int. Ed. 1983, 22, 796-797.
-
(1983)
Angew. Chem. Int. Ed.
, vol.22
, pp. 796-797
-
-
Hoffman, H.R.M.1
Rabe, J.2
-
41
-
-
0026076065
-
A kinetic and mechanistic study of the baylis-hillman reaction
-
Bode, M.L.; Kaye, P.T. A kinetic and mechanistic study of the Baylis-Hillman reaction. Tetrahedron Lett. 1991, 32, 5611-5614.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5611-5614
-
-
Bode, M.L.1
Kaye, P.T.2
-
42
-
-
0026705601
-
The Baylis-Hillman reaction-Mechanism and applications revisited
-
Fort, Y.; Berthe, M.C.; Caubère, P. The Baylis-Hillman reaction-Mechanism and applications revisited. Tetrahedron 1992, 48, 6371-6384.
-
(1992)
Tetrahedron
, vol.48
, pp. 6371-6384
-
-
Fort, Y.1
Berthe, M.C.2
Caubére, P.3
-
43
-
-
0027304411
-
Effect of solvent, pressure and catalyst on the e/z selectivity in the baylis-hillman reaction between crotononitrile and benzaldehyde
-
Rozendaal, E.M.L., Voss, B.M.W.; Scheeren, H.W. Effect of solvent, pressure and catalyst on the E/Z selectivity in the Baylis-Hillman reaction between crotononitrile and benzaldehyde. Tetrahedron 1993, 49, 6931-6936.
-
(1993)
Tetrahedron
, vol.49
, pp. 6931-6936
-
-
Rozendaal, E.M.L.1
Voss, B.M.W.2
Scheeren, H.W.3
-
44
-
-
15744383666
-
Chiral phosphine lewis bases catalyzed asymmetric aza-baylis- hillman reaction of n-sulfonated imines with activated olefins
-
Shi, M.; Chen, L.-H.; Li, C.-Q. Chiral phosphine Lewis bases catalyzed asymmetric aza-Baylis- Hillman reaction of N-sulfonated imines with activated olefins. J. Am. Chem. Soc. 2005, 127, 3790-3800.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3790-3800
-
-
Shi, M.1
Chen, L.-H.2
Li, C.-Q.3
-
45
-
-
4544278079
-
Probing the mechanism of the baylis-hillman reaction by electrospray ionization mass and tandem mass spectrometry.
-
Santos, L.S., Pavam, C.H.; Almeida, W.P.; Coelho, F.; Eberlin, M.N. Probing the mechanism of the Baylis-Hillman reaction by electrospray ionization mass and tandem mass spectrometry. Angew. Chem. Int. Ed. 2004, 43, 4330-4333.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 4330-4333
-
-
Santos, L.S.1
Pavam, C.H.2
Almeida, W.P.3
Coelho, F.4
Eberlin, M.N.5
-
46
-
-
27544480807
-
Highly enantioselective aza-baylis-hillman reactions catalyzed by chiral thiourea derivatives
-
Raheem, I.T.; Jacobsen, E.N. Highly Enantioselective Aza-Baylis-Hillman Reactions Catalyzed by Chiral Thiourea Derivatives. Adv. Synth. Catal. 2005, 347, 1701-1708.
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1701-1708
-
-
Raheem, I.T.1
Jacobsen, E.N.2
-
47
-
-
0028197521
-
Improved syntheses of ethyl(a-bromomethyl)acrylate and 2-methylene-1,3-propanediol via ethyl a-(hydroxymethyl) acrylate
-
Byun, H.S.; Reddy, K.C.; Bittman, R. Improved syntheses of ethyl(a-bromomethyl)acrylate and 2-methylene-1,3-propanediol via ethyl a-(hydroxymethyl) acrylate. Tetrahedron Lett. 1994, 35, 1371-1374.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 1371-1374
-
-
Byun, H.S.1
Reddy, K.C.2
Bittman, R.3
-
48
-
-
0027974067
-
Acceleration in water of the baylis-hillman reaction
-
Auge, J.; Lubin, N.; Lubineau, A. Acceleration in water of the Baylis-Hillman reaction. Tetrahedron Lett. 1994, 35, 7947-7948.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 7947-7948
-
-
Auge, J.1
Lubin, N.2
Lubineau, A.3
-
49
-
-
0034026611
-
The aqueous trimethylamine mediated baylis- hillman reaction
-
Basavaiah, D.; Krishnamacharyulu, M. Rao, A.J. The Aqueous Trimethylamine Mediated Baylis- Hillman Reaction. Synth. Commun. 2000, 30, 2061-2069.
-
(2000)
Synth. Commun.
, vol.30
, pp. 2061-2069
-
-
Basavaiah, D.1
Krishnamacharyulu, M.2
Rao, A.J.3
-
50
-
-
0035838860
-
Efficient baylis-hillman reaction using stoichiometric base catalyst and an aqueous medium
-
Yu, C.Z.; Liu, B.; Hu, L.Q. Efficient Baylis-Hillman Reaction Using Stoichiometric Base Catalyst and an Aqueous Medium. J. Org. Chem. 2001, 66, 5413-5418.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 5413-5418
-
-
Yu, C.Z.1
Liu, B.2
Hu, L.Q.3
-
51
-
-
0013308184
-
Dramatic rate acceleration of the baylis-hillman reaction in homogeneous medium in the presence of water
-
Cai, J.; Zhou, Z.; Zhao, G.; Tang, C. Dramatic Rate Acceleration of the Baylis-Hillman Reaction in Homogeneous Medium in the Presence of Water. Org. Lett. 2002, 4, 4723-4725.
-
(2002)
Org. Lett.
, vol.4
, pp. 4723-4725
-
-
Cai, J.1
Zhou, Z.2
Zhao, G.3
Tang, C.4
-
52
-
-
33847414560
-
Octanol-accelerated baylis-hillman reaction
-
Park, K.S.; Kim, J.; Choo, H.; Chong, Y. Octanol-Accelerated Baylis-Hillman Reaction. Synlett. 2007, 395-398.
-
(2007)
Synlett
, pp. 395-398
-
-
Park, K.S.1
Kim, J.2
Choo, H.3
Chong, Y.4
-
53
-
-
33744469835
-
Traditional morita-baylis-hillman reaction of aldehydes with methyl vinyl ketone co-catalyzed with triphenylphosphine and nitrophenol
-
Shi, M.; Liu, Y.H. Traditional Morita-Baylis-Hillman reaction of aldehydes with methyl vinyl ketone co-catalyzed with triphenylphosphine and nitrophenol. Org. Biomol. Chem. 2006, 4, 1468-1470.
-
(2006)
Org. Biomol. Chem.
, vol.4
, pp. 1468-1470
-
-
Shi, M.1
Liu, Y.H.2
-
54
-
-
0032556396
-
Asymmetric baylis-hillman reaction: catalysis using a chiral pirrolizidine base
-
Barrett, A.G.M.; Cook, A.S.; Kamimura, A. Asymmetric Baylis-Hillman reaction: catalysis using a chiral pirrolizidine base. Chem. Commun. 1998, 2533-2534.
-
(1998)
Chem. Commun.
, pp. 2533-2534
-
-
Barrett, A.G.M.1
Cook, A.S.2
Kamimura, A.3
-
55
-
-
84947191160
-
Synthesis of 3-hydroxy-2-methylene carbonyl compounds
-
Drewes, S.E.; Freese, S.D.; Emslie, N.D.; Roos, G.H.P. Synthesis of 3-Hydroxy-2-Methylene Carbonyl Compounds. Synth. Commun. 1988, 18, 1565-1572.
-
(1988)
Synth. Commun.
, vol.18
, pp. 1565-1572
-
-
Drewes, S.E.1
Freese, S.D.2
Emslie, N.D.3
Roos, G.H.P.4
-
56
-
-
0025334578
-
Stereoselective epoxidation of hydroxyenones. the synthesis of the sidechain of clerocidin
-
Bailey, M. ; Markó, I.E.; Ollis, W.D., Rasmussen, P.R. Stereoselective epoxidation of hydroxyenones. The synthesis of the sidechain of clerocidin. Tetrahedron Lett. 1990, 31, 4509-4512.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 4509-4512
-
-
Bailey, M.1
Markó, I.E.2
Ollis, W.D.3
Rasmussen, P.R.4
-
57
-
-
0141743697
-
β-Isocupreidine-catalyzed Asymmetric Baylis-Hillman Reaction of Imines
-
Kawahara, S.; Nakano, A.; Esumi, T.; Iwabuchi, Y.; Hatakeyama, S. β-Isocupreidine-catalyzed Asymmetric Baylis-Hillman Reaction of Imines. Org. Lett. 2003, 5, 3103.
-
(2003)
Org. Lett.
, vol.5
, pp. 3103
-
-
Kawahara, S.1
Nakano, A.2
Esumi, T.3
Iwabuchi, Y.4
Hatakeyama, S.5
-
58
-
-
0037011306
-
Catalytic asymmetric baylis-hillman reaction of imines with methyl vinyl ketone and methyl acrylate
-
Shi, M.; Xu, Y-M. Catalytic, Asymmetric Baylis-Hillman Reaction of Imines with Methyl Vinyl Ketone and Methyl Acrylate. Angew. Chem. Int. Ed. 2002, 41, 4507.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 4507
-
-
Shi, M.1
Xu, Y-M.2
-
59
-
-
53849125824
-
A Novel Selective Aza-Morita-Baylis-Hillman (aza-MBH) domino reaction and aza-MBH reaction of N-Sulfonyl imines with acrolein catalyzed by bifunctional phosphine organocatalyst
-
Meng, X.; Huang, Y.; Chen, R. A Novel Selective Aza-Morita-Baylis-Hillman (aza-MBH) Domino Reaction and aza-MBH Reaction of N-Sulfonyl Imines with Acrolein Catalyzed by Bifunctional Phosphine Organocatalyst. Chem. Eur. J. 2008, 14, 6852-6856.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 6852-6856
-
-
Meng, X.1
Huang, Y.2
Chen, R.3
-
60
-
-
33645395732
-
A brönsted acid and lewis base organocatalyst for the aza- morita-baylis-hillman reaction
-
Matsui, K.; Takizawa, S.; Sasai. H. A Brönsted acid and Lewis base organocatalyst for the aza- Morita-Baylis-Hillman reaction. Synlett. 2006, 761-765.
-
(2006)
Synlett
, pp. 761-765
-
-
Matsui, K.1
Takizawa, S.2
Sasai., H.3
-
61
-
-
12344286314
-
Baylis-hillman mechanism: A new interpretation in aprotic solvents
-
Price, K.E.; Broadwater, S.J.; Jung, H.M.; McQuade, D.T. Baylis-Hillman mechanism: A New Interpretation in Aprotic Solvents. Org. Lett. 2005, 7, 147-150.
-
(2005)
Org. Lett.
, vol.7
, pp. 147-150
-
-
Price, K.E.1
Broadwater, S.J.2
Jung, H.M.3
McQuade, D.T.4
-
62
-
-
18744378020
-
A new interpretation of the baylis-hillman mechanism
-
Price, K.E.; Broadwater, S.J.; Walker, B.J.; McQuade, D.T. A new interpretation of the Baylis-Hillman mechanism. J. Org. Chem. 2005, 70, 3980-3987.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 3980-3987
-
-
Price, K.E.1
Broadwater, S.J.2
Walker, B.J.3
McQuade, D.T.4
-
63
-
-
17044437071
-
Re-evaluation of the mechanism of the baylis-hillman reaction - implications for asymmetric catalysis.
-
Aggarwal, V.K.; Fulford, F.Y.; Lloyd-Jones, G.C. Re-evaluation of the mechanism of the Baylis-Hillman reaction - implications for asymmetric catalysis. Angew. Chem. Int. Ed. 2005, 44, 1706-1708.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 1706-1708
-
-
Aggarwal, V.K.1
Fulford, F.Y.2
Lloyd-Jones, G.C.3
-
64
-
-
37849014325
-
Mechanism of the morita-baylis-hillman reaction: A computational investigation
-
Robiette, R.; Aggarwal, V.K.; Harvey, J.N. Mechanism of the Morita-Baylis-Hillman reaction: A computational investigation. J. Am. Chem. Soc. 2007, 129, 15513-15525.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 15513-15525
-
-
Robiette, R.1
Aggarwal, V.K.2
Harvey, J.N.3
-
65
-
-
65249127674
-
Dualistic nature of the mechanism of the morita-baylis-hillman reaction probed by electrospray ionization mass spectrometry
-
Amarante, G.W.; Milagre, H.M.S.; Vaz, B.G.; Ferreira, B.R.V.; Eberlin, M.C.; Coelho, F. Dualistic nature of the mechanism of the Morita-Baylis-Hillman reaction probed by electrospray ionization mass spectrometry. J. Org. Chem. 2009, 74, 3031-3037.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 3031-3037
-
-
Amarante, G.W.1
Milagre, H.M.S.2
Vaz, B.G.3
Ferreira, B.R.V.4
Eberlin, M.C.5
Coelho, F.6
-
66
-
-
70350474380
-
The morita-baylis-hillman reaction: Insights into asymmetry and reaction mechanisms by electrospray ionization mass spectrometry
-
Carrasco-Sanchez, V.; Simirgiotis, M.J.; Santos, L.S. The Morita-Baylis-Hillman reaction: insights into asymmetry and reaction mechanisms by electrospray ionization mass spectrometry. Molecules 2009, 14, 3989-4021.
-
(2009)
Molecules
, vol.14
, pp. 3989-4021
-
-
Carrasco-Sanchez, V.1
Simirgiotis, M.J.2
Santos, L.S.3
-
67
-
-
38349097338
-
Online mechanistic investigations of catalyzed reactions by electrospray ionization mass spectrometry: A tool to intercept transient species in solution
-
Online mechanistic investigations of catalyzed reactions by electrospray ionization mass spectrometry: A tool to intercept transient species in solution. Eur. J. Org. Chem. 2008, 235-253.
-
(2008)
Eur. J. Org. Chem.
, pp. 235-253
-
-
-
68
-
-
28844451041
-
Bifunctional activation and racemization in the catalytic asymmetric aza-baylis-hillman reaction
-
Buskens, P.; Klankermayer, J.; Leitner, W. Bifunctional Activation and Racemization in the Catalytic Asymmetric aza-Baylis-Hillman Reaction. J. Am. Chem. Soc. 2005, 127, 16762-16763.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 16762-16763
-
-
Buskens, P.1
Klankermayer, J.2
Leitner, W.3
-
69
-
-
34249712553
-
A way to highly enantiomerically enriched aza-morita-baylis-hillman-type products
-
Utsumi, N.; Zhang, H.; Tanaka, F.; Barbas, C.B., III. A Way to Highly Enantiomerically Enriched aza-Morita-Baylis-Hillman-Type Products. Angew. Chem. Int. Ed. 2007, 46, 1878-1880.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 1878-1880
-
-
Utsumi, N.1
Zhang, H.2
Tanaka, F.3
Barbas III, C.B.4
-
70
-
-
24944559389
-
Dual catalyst control in the enantioselective intramolecular morita-baylis-hillman reaction
-
Aroyan, C.E.; Vasbinder, M.M.; Miller, S.J. Dual Catalyst Control in the Enantioselective Intramolecular Morita-Baylis-Hillman Reaction. Org. Lett. 2005, 7, 3849-3851.
-
(2005)
Org. Lett.
, vol.7
, pp. 3849-3851
-
-
Aroyan, C.E.1
Vasbinder, M.M.2
Miller, S.J.3
-
71
-
-
4143141139
-
In search of peptide-based catalysts for asymmetric organic synthesis
-
Miller, S.J. In Search of Peptide-Based Catalysts for Asymmetric Organic Synthesis. Acc. Chem. Res. 2004, 37, 601-610.
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 601-610
-
-
Miller, S.J.1
-
72
-
-
0142042898
-
Dual catalyst control in the amino acid-peptide- catalyzed enantioselective baylis-hillman reaction
-
Imbriglio, J.E.; Vasbinder, M.M.; Miller, S.J. Dual Catalyst Control in the Amino Acid-Peptide- Catalyzed Enantioselective Baylis-Hillman Reaction. Org. Lett. 2003, 5, 3741-3743.
-
(2003)
Org. Lett.
, vol.5
, pp. 3741-3743
-
-
Imbriglio, J.E.1
Vasbinder, M.M.2
Miller, S.J.3
-
73
-
-
33750437400
-
Amino acid-peptide-catalyzed enantioselective Morita-Baylis-Hillman reactions
-
Vasbinder, M.M.; Imbriglio, J.E.; Miller, S.J. Amino acid-peptide- catalyzed enantioselective Morita-Baylis-Hillman reactions. Tetrahedron 2006, 62, 11450-11459.
-
(2006)
Tetrahedron
, vol.62
, pp. 11450-11459
-
-
Vasbinder, M.M.1
Imbriglio, J.E.2
Miller, S.J.3
-
74
-
-
34548249167
-
Aza-morita-baylis-hillman-type reactions: highly enantioselective addition of unmodified a,β-unsaturated aldehydes with n-boc protected imines
-
Vesely, J.; Dziedzic, P.; Csrdova, A. Aza-Morita-Baylis-Hillman-type reactions: highly enantioselective addition of unmodified a,β-unsaturated aldehydes with N-Boc protected imines. Tetrahedron Lett. 2007, 48, 6900-6904.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 6900-6904
-
-
Vesely, J.1
Dziedzic, P.2
Córdova, A.3
-
75
-
-
0036134467
-
Lewis base and L-proline co-catalyzed baylis-hillman reaction of arylaldehydes and methyl vinyl ketone
-
Shi, M.; Jiang, J.-K.; Li, C.-Q. Lewis base and L-proline co-catalyzed Baylis-Hillman reaction of arylaldehydes and methyl vinyl ketone. Tetrahedron Lett. 2002, 43, 127-130.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 127-130
-
-
Shi, M.1
Jiang, J.-K.2
Li, C.-Q.3
-
76
-
-
27944479071
-
An unexpected inversion of enantioselectivity in the proline catalyzed intramolecular baylis-hillman reaction
-
Chen, S.-H.; Hong, B.-C.; Su, C.-F.; Sarshar, S. An unexpected inversion of enantioselectivity in the proline catalyzed intramolecular Baylis-Hillman reaction. Tetrahedron Lett. 2005, 46, 8899-8903.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8899-8903
-
-
Chen, S.-H.1
Hong, B.-C.2
Su, C.-F.3
Sarshar, S.4
-
77
-
-
60749108597
-
Density functional study of prolinecatalyzed intramolecular baylis-hillman reactions
-
Duarte, F.J.S.; Cabrita, E.J.; Frenking, G., Santos, A.G. Density functional study of prolinecatalyzed intramolecular Baylis-Hillman Reactions. Chem. Eur. J. 2009, 15, 1734-1746.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 1734-1746
-
-
Duarte, F.J.S.1
Cabrita, E.J.2
Frenking, G.3
Santos, A.G.4
-
78
-
-
0000369178
-
Aldol reactions of allenolates generated by 1,4-addition of iodide anion or its equivalent to acetylenic ketones
-
Taniguchi, M.; Hino, T.; Kishi, Y. Aldol reactions of allenolates generated by 1,4-addition of iodide anion or its equivalent to acetylenic ketones. Tetrahedron Lett. 1986, 27, 4767-4770.
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 4767-4770
-
-
Taniguchi, M.1
Hino, T.2
Kishi, Y.3
-
79
-
-
0000000271
-
Highly stereoselective coupling reaction of acrolein or vinyl ketone with aldehydes
-
Uehira, S.; Nan, Z.; Shinokubo, H.; Oshima K. Highly Stereoselective coupling reaction of acrolein or vinyl ketone with aldehydes. Org. Lett. 1999, 1, 1383-1385.
-
(1999)
Org. Lett.
, vol.1
, pp. 1383-1385
-
-
Uehira, S.1
Nan, Z.2
Shinokubo, H.3
Oshima, K.4
-
80
-
-
0035945010
-
Substoichiometric TiCl4-mediated vicinal difunctionalization of a,β- acetylenic ketones for the synthesis of β-halo baylis-hillman olefins
-
Wei, H.X.; Gao J.J.; Li, G. Substoichiometric TiCl4-mediated vicinal difunctionalization of a,β- acetylenic ketones for the synthesis of β-halo Baylis-Hillman olefins. Tetrahedron Lett. 2001, 42, 9119-9122.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 9119-9122
-
-
Wei, H.X.1
Gao, J.J.2
Li, G.3
-
81
-
-
11944259320
-
Chalcogenide-lewis acid mediated tandem michael aldol reaction. an alternative to the morita-baylis-hillman reaction and a new development
-
Kataoka, T.; Kinoshita, H. Chalcogenide-lewis acid mediated tandem michael aldol reaction. An alternative to the morita-baylis-hillman reaction and a new development. Eur. J. Org. Chem. 2005, 45-48.
-
(2005)
Eur. J. Org. Chem.
, pp. 45-48
-
-
Kataoka, T.1
Kinoshita, H.2
-
82
-
-
0037023405
-
Titanium isopropoxide as efficient catalyst for the Aza-Baylis-Hillman Reaction. selective formation of a-methylene-β-amino acid derivatives
-
Balan, D.; Adolfsson, H. titanium isopropoxide as efficient catalyst for the Aza-Baylis-Hillman Reaction. selective formation of a-methylene-β-amino acid derivatives. J. Org. Chem. 2002, 67, 2329-2334.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 2329-2334
-
-
Balan, D.1
Adolfsson, H.2
-
84
-
-
0001400106
-
Quaternary ammonium enolates as synthetic intermediates. Regiospecific alkylation reaction of ketones
-
Kuwajima, I.; Nakamura, E. Quaternary Ammonium Enolates as Synthetic Intermediates. Regiospecific Alkylation Reaction of Ketones. J. Am. Chem. Soc. 1975, 97, 3257-3258.
-
(1975)
J. Am. Chem. Soc.
, vol.97
, pp. 3257-3258
-
-
Kuwajima, I.1
Nakamura, E.2
-
85
-
-
0000456862
-
Tris(dimethylamine) sulfonium Enolates
-
Noyori, R.; Nishida, I.; Sakata, J.; Nishizawa, M. Tris(dimethylamine) sulfonium Enolates. J. Am. Chem. Soc. 1980, 102, 1223-1225.
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 1223-1225
-
-
Noyori, R.1
Nishida, I.2
Sakata, J.3
Nishizawa, M.4
-
87
-
-
33847088879
-
Fluoride ion catalyzed aldol reaction between enol silyl ethers and carbonyl compound
-
Noyori, R.; Yokoyama, K.; Sakata, J.; Kuwajima, I.; Nakamura, E. Fluoride ion catalyzed Aldol Reaction between enol silyl ethers and carbonyl compounds J. Am. Chem. Soc. 1977, 99, 1265-1267.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 1265-1267
-
-
Noyori, R.1
Yokoyama, K.2
Sakata, J.3
Kuwajima, I.4
Nakamura, E.5
-
88
-
-
9544223606
-
Stereoselection in aldol condensation
-
Kleshick, W.A.; Buse, C.T.; Heathcock, C.H. Stereoselection in aldol condensation J. Am. Chem. Soc. 1977, 99, 247-248.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 247-248
-
-
Kleshick, W.A.1
Buse, C.T.2
Heathcock, C.H.3
-
89
-
-
77649205000
-
-
- for nomenclature
-
Notice that for the case of unsaturated esters this intermediate is in fact the E enolate as OMe has precedence over the O- for nomenclature.
-
-
-
-
91
-
-
0345863483
-
An unexpected rate acceleration-practical improvements in the baylis- hillman reaction
-
Rafel, S.; Leahy, J.W. An Unexpected rate acceleration-practical improvements in the Baylis- Hillman Reaction. J. Org. Chem. 1997, 62, 1521-1522.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1521-1522
-
-
Rafel, S.1
Leahy, J.W.2
-
92
-
-
37849014325
-
Mechanism of the morita-baylis-hillman reaction: A computational investigation
-
Robiette, R.; Aggarwal, V.K.; Harvey, J.N. Mechanism of the Morita-Baylis-Hillman reaction: A computational investigation. J. Am. Chem. Soc. 2007, 129, 15513-15525.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 15513-15525
-
-
Robiette, R.1
Aggarwal, V.K.2
Harvey, J.N.3
-
93
-
-
33645467341
-
Implications in the morita-baylis-hillman alkylation: Isolation and characterization of an intermediate
-
Kraftt, M.E.; Haxell, T.F.N.; Seibert, K.A.; Abboud, K.A. Implications in the Morita-Baylis-Hillman Alkylation: Isolation and Characterization of an Intermediate. J. Am. Chem. Soc. 2006, 128, 4174-4175.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4174-4175
-
-
Kraftt, M.E.1
Haxell, T.F.N.2
Seibert, K.A.3
Abboud, K.A.4
-
94
-
-
0037016618
-
The aldol addition reaction : An old transformation at constant rebirth
-
Reviews on catalytic enantioselective condensations
-
Reviews on catalytic enantioselective condensations: Palomo, C.; Oiarbide, M.; García, J.M. The Aldol Addition Reaction : An Old Transformation at Constant Rebirth. Chem. Eur. J. 2002, 8, 36-44.
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 36-44
-
-
Palomo, C.1
Oiarbide, M.2
Garcĺa, J.M.3
-
95
-
-
0037463084
-
The direct catalytic asymmetric cross-aldol reaction of aldehydes
-
Alcaide, B.; Almendros, P. The Direct Catalytic Asymmetric Cross-Aldol Reaction of Aldehydes. Angew. Chem. Int. Ed. 2003, 42, 858.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 858
-
-
Alcaide, B.1
Almendros, P.2
-
96
-
-
0000851696
-
-
Trost, B.M., Fleming, I., Heathcock, C.H., Eds.; Pergamon: Oxford, UK
-
Heathcock, C.H. Comprehensive Organic Synthesis; Trost, B.M., Fleming, I., Heathcock, C.H., Eds.; Pergamon: Oxford, UK, 1991; Volume 2, pp. 133-176.
-
(1991)
Comprehensive Organic Synthesis
, vol.2
, pp. 133-176
-
-
Heathcock, C.H.1
-
97
-
-
31144439127
-
Influence of michael acceptor stereochemistry on intramolecular morita-baylis-hillman reactions
-
Teng, W.-D.; Huang, R.; Kwong, C.K.-W.; Shi, M.; Toy, P.H. Influence of Michael Acceptor Stereochemistry on Intramolecular Morita-Baylis-Hillman Reactions. J. Org. Chem. 2006, 71, 368-371.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 368-371
-
-
Teng, W.-D.1
Huang, R.2
Kwong, C.K.-W.3
Shi, M.4
Toy, P.H.5
-
98
-
-
0000584420
-
-
Morrison, J.D., Ed.; Academic Press, Inc.: New York, NY, USA
-
Heathcock, C.H. Asymmetric Syntheis; Morrison, J.D., Ed.; Academic Press, Inc.: New York, NY, USA, 1984; Volume 3, pp. 111-212.
-
(1984)
Asymmetric Syntheis
, vol.3
, pp. 111-212
-
-
Heathcock, C.H.1
-
99
-
-
0000507168
-
-
Pergamon: Oxford, UK
-
Trost, B.M; Fleming, I.; Heathcock, C.H. Comprehensive Organic Synthesis; Pergamon: Oxford, UK, 1991; Volume 2, pp. 173-179.
-
(1991)
Comprehensive Organic Synthesis
, vol.2
, pp. 173-179
-
-
Trost, B.M.1
Fleming, I.2
Heathcock, C.H.3
-
100
-
-
0001438016
-
Erytro-selective aldol reaction via tris(dimethylamine)sulfonium enolates
-
Noyori, R.; Nishida, I.; Sakata, J. Erytro-selective aldol reaction via tris(dimethylamine)sulfonium enolates. J. Am. Chem. Soc. 1981, 103, 2106-2108.
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 2106-2108
-
-
Noyori, R.1
Nishida, I.2
Sakata, J.3
-
101
-
-
0000923060
-
Tris(dialkylamine) sulfonium enolates. Synthesis, structure and reactions
-
Noyori, R.; Nishida, I.; Sakata, J.; Nishizawa, M. Tris(dialkylamine) sulfonium enolates. Synthesis, structure and reactions. J. Am. Chem. Soc. 1983, 105, 1598-1608.
-
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 1598-1608
-
-
Noyori, R.1
Nishida, I.2
Sakata, J.3
Nishizawa, M.4
-
102
-
-
33947468884
-
The stereochemistry of the ivanov and reformatsky reactions
-
Zimmerman, H.E.; Traxler, M.D. The Stereochemistry of the Ivanov and Reformatsky Reactions. J. Am. Chem. Soc. 1957, 79, 1920-1923.
-
(1957)
J. Am. Chem. Soc.
, vol.79
, pp. 1920-1923
-
-
Zimmerman, H.E.1
Traxler, M.D.2
-
103
-
-
77649212854
-
-
According to nomenclature employed by Noyori's group at the eighties syn aldols were named as erythro and anti aldols were named as threo
-
According to nomenclature employed by Noyori's group at the eighties syn aldols were named as erythro and anti aldols were named as threo.
-
-
-
-
104
-
-
32644447711
-
Dynamic stereochemistry of aldolization-xxi. definition of "restoring energy" of a system of reversible competitive reactions.
-
Dubois, J-E., Fort, J.-F. Dynamic stereochemistry of aldolization-XXI. Definition of "restoring energy" of a system of reversible competitive reactions. Tetrahedron 1972, 28, 1665-1675.
-
(1972)
Tetrahedron
, vol.28
, pp. 1665-1675
-
-
Dubois, J-E.1
Fort, J.-F.2
-
105
-
-
33847086576
-
Trialkylsilyl triflates. 5. a stereoselective aldol-type condensation of enol silyl ethers and acetals catalyzed by trimethylsilyl trifluoromethanesulfonate
-
Murata, S.; Suzuki, M.; Noyori, R. Trialkylsilyl triflates. 5. A stereoselective aldol-type condensation of enol silyl ethers and acetals catalyzed by trimethylsilyl trifluoromethanesulfonate. J. Am. Chem. Soc. 1980, 102, 3248-3249.
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 3248-3249
-
-
Murata, S.1
Suzuki, M.2
Noyori, R.3
-
106
-
-
33845373936
-
Acyclic stereoselection. 36. simple diastereoselection in the lewis acid mediated reactions of enol silanes with aldehydes
-
Heathcock, C.H.; Davidsen, S.K.; Flippin, L.A. Acyclic stereoselection. 36. Simple diastereoselection in the Lewis acid mediated reactions of enol silanes with aldehydes. J. Org. Chem. 1986, 51, 3027-3037.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 3027-3037
-
-
Heathcock, C.H.1
Davidsen, S.K.2
Flippin, L.A.3
-
107
-
-
15744387149
-
Lewis base activation of lewis acids: Catalytic, enantioselective addition of silyl ketene acetals to aldehydes.
-
Denmark, S.E; Beutner, G.L.; Wynn, T.; Eastgate, M.D. Lewis base activation of lewis acids: catalytic, enantioselective addition of silyl ketene acetals to aldehydes. J. Am. Chem. Soc. 2005, 127, 3774-3789.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3774-3789
-
-
Denmark, S.E.1
Beutner, G.L.2
Wynn, T.3
Eastgate, M.D.4
-
108
-
-
41949101219
-
Lewis base activation of lewis acids: Catalytic enantioselective glycolate aldol reactions
-
Denmark, S.; Chung, W.-j. Lewis Base activation of lewis acids: catalytic enantioselective glycolate aldol reactions. Angew. Chem. Int. Ed. 2008, 47, 1890-1892.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 1890-1892
-
-
Denmark, S.1
Chung, W.-j.2
-
109
-
-
52449119366
-
Highly enantioselective aza morita-baylis-hillman reaction catalyzed by bifunctional β-isocupreidine derivatives
-
Abermil, M.; Masson, G.; Zhu, J. Highly Enantioselective aza Morita-Baylis-Hillman Reaction Catalyzed by Bifunctional β-isocupreidine Derivatives. J. Am. Chem. Soc. 2008, 130, 12596-12597.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 12596-12597
-
-
Abermil, M.1
Masson, G.2
Zhu, J.3
-
110
-
-
70349934416
-
Invertible enantioselectivity in 6'-deoxy-6'-acylamino-β- isocupreidine-catalyzed aza-morita-baylis-hillman reaction: Key role of an achiral additive
-
Abermil, M.; Masson, G.; Zhu, J. Invertible Enantioselectivity in 6'-Deoxy-6'-acylamino-β- Isocupreidine-catalyzed Aza-Morita-Baylis-Hillman Reaction: Key Role of an Achiral Additive. Org. Lett. 2009, 11, 4648-4651.
-
(2009)
Org. Lett.
, vol.11
, pp. 4648-4651
-
-
Abermil, M.1
Masson, G.2
Zhu, J.3
-
111
-
-
0033520752
-
Chiral amine-catalyzed asymmetric baylis-hillman reaction: A reliable route to highly enantiomerically-enriched to (α-methylene- β-hydroxy)esters
-
Ibawuchi, Y.; Nakatani, M.?Yokoyama, N.; Hatakeyama, S. Chiral amine-catalyzed asymmetric Baylis-Hillman reaction: A reliable route to highly enantiomerically-enriched to (α-Methylene- β-hydroxy)esters. J. Am. Chem. Soc. 1999, 121, 10219-10220.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 10219-10220
-
-
Ibawuchi, Y.1
Nakatani, M.2
Yokoyama, N.3
Hatakeyama, S.4
-
112
-
-
68149144269
-
Diastereo-and enantioselective aza-mbh-type reaction of nitroalkenes to n-tosylimines catalyzed by bifunctional organocatalysts
-
Wang, X.; Chen, Y.-F.; Niu L.-F.; Xu, P.-X. Diastereo- and enantioselective aza-mbh-type reaction of nitroalkenes to n-tosylimines catalyzed by bifunctional organocatalysts. Org. Lett. 2009, 11, 3310-3313.
-
(2009)
Org. Lett.
, vol.11
, pp. 3310-3313
-
-
Wang, X.1
Chen, Y.-F.2
Niu, L.-F.3
Xu, P.-X.4
-
113
-
-
37049135746
-
The aldol condensation: Influence of the solvent and the cation on stereoselectivity
-
Dubois, J.E.; Dubois, M. The aldol condensation: influence of the solvent and the cation on stereoselectivity. Chem Commun. 1968, 1567-1568.
-
(1968)
Chem Commun.
, pp. 1567-1568
-
-
Dubois, J.E.1
Dubois, M.2
-
114
-
-
36349022163
-
Ab initio and density functional theory evidence on the rate-limiting step in the morita-baylis-hillman reaction
-
Roy, D.; Sunoj, R.B. Ab Initio and Density Functional Theory Evidence on the Rate-Limiting Step in the Morita-Baylis-Hillman Reaction. Org. Lett. 2007, 9, 4873-4876.
-
(2007)
Org. Lett.
, vol.9
, pp. 4873-4876
-
-
Roy, D.1
Sunoj, R.B.2
-
115
-
-
56749131127
-
Water catalysis in the morita-baylis-hillman reaction: A mechanistic perspective
-
Roy, D.; Sunoj, R.B. Water Catalysis in the Morita-Baylis-Hillman Reaction: A Mechanistic Perspective. Chem. Eur. J. 2008, 14, 10530-10534.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 10530-10534
-
-
Roy, D.1
Sunoj, R.B.2
-
116
-
-
67049110205
-
DFT study on the role of methanol solvent in morita-baylis- hillman reaction
-
See also [62]
-
Fan, J.-F.; Yang, C.-H.; He, L.-J. DFT Study on the Role of Methanol Solvent in Morita-Baylis- Hillman Reaction. J. Int. Q. Chem. 2009, 109, 1311-1321. See also [62].
-
(2009)
J. Int. Q. Chem.
, vol.109
, pp. 1311-1321
-
-
Fan, J.-F.1
Yang, C.-H.2
He, L.-J.3
-
117
-
-
33747876396
-
Probing the mechanism of morita-baylis-hillman reaction in dichloromethane by density functional theory
-
See also [62]
-
Xu, J. Probing the mechanism of Morita-Baylis-Hillman reaction in dichloromethane by density functional theory. J. Mol. Struct. (TeoChem.) 2006, 767, 61-66. See also [62].
-
(2006)
J. Mol. Struct. (TeoChem.)
, vol.767
, pp. 61-66
-
-
Xu, J.1
-
118
-
-
60849113441
-
Enantioselective trifunctional organocatalysis for rate- enhanced aza-morita-baylis-hillman reactions at room temperature
-
Garnier, J.-M.; Anstiss, C.; Liu, F. Enantioselective Trifunctional Organocatalysis for Rate- Enhanced aza-Morita-Baylis-Hillman Reactions at Room Temperature. Adv. Synth. Catal. 2009, 351, 331-338.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 331-338
-
-
Garnier, J.-M.1
Anstiss, C.2
Liu, F.3
-
119
-
-
67649403306
-
Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-morita-baylis-hillman reactions at ambient temperature
-
Garnier, J.-M.; Liu, F. Trifunctional organocatalyst-promoted counterion catalysis for fast and enantioselective aza-Morita-Baylis-Hillman reactions at ambient temperature. Org. Biomol. Chem. 2009, 7, 1272-1275.
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 1272-1275
-
-
Garnier, J.-M.1
Liu, F.2
-
120
-
-
45049083371
-
A rationally designed cocatalyst for the morita-baylis-hillman reaction
-
Jones, C.E.S.; Turega, S.M.; Clarke, M.L.; Philp, D. A rationally designed cocatalyst for the Morita-Baylis-Hillman reaction. Tetrahedron Lett. 2008, 49, 4666-4669.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4666-4669
-
-
Jones, C.E.S.1
Turega, S.M.2
Clarke, M.L.3
Philp, D.4
-
121
-
-
50949101490
-
Chiral phosphinothiourea organocatalyst in the enantioselective morita-baylis-hillman reactions of aromatic aldehydes with methyl vinyl ketone
-
Yuan, K.; Zhang, L.; Song, H.-L.; Hu, Y.; Wu, X.-Y. Chiral phosphinothiourea organocatalyst in the enantioselective Morita-Baylis-Hillman reactions of aromatic aldehydes with methyl vinyl ketone. Tetrahedron Lett. 2008, 49, 6262-6264.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 6262-6264
-
-
Yuan, K.1
Zhang, L.2
Song, H.-L.3
Hu, Y.4
Wu, X.-Y.5
-
122
-
-
25444432564
-
Chiral binaphthyl-derived amine-thiourea organocatalyst-promoted asymmetric morita-baylis-hillman reaction
-
Wang, J.; Li, H.; Yu, X.; Zu, L.; Wang, W. Chiral binaphthyl-derived amine-thiourea organocatalyst-promoted asymmetric Morita-Baylis-Hillman reaction. Org. Lett. 2005, 7, 4293-4296.
-
(2005)
Org. Lett.
, vol.7
, pp. 4293-4296
-
-
Wang, J.1
Li, H.2
Yu, X.3
Zu, L.4
Wang, W.5
-
123
-
-
49349094494
-
Thiourea-catalyzed morita-baylis-hillman reaction
-
Sohtome, Y.; Takemura, N.; Takagi, R.; Hashimoto, Y.; Nagasawa, K. Thiourea-catalyzed Morita-Baylis-Hillman reaction. Tetrahedron 2008, 64, 9423-9429.
-
(2008)
Tetrahedron
, vol.64
, pp. 9423-9429
-
-
Sohtome, Y.1
Takemura, N.2
Takagi, R.3
Hashimoto, Y.4
Nagasawa, K.5
-
124
-
-
0141923582
-
Asymmetric morita-baylis-hillman reactions catalyzed by chiral brønsted acids
-
McDougal, N. T.; Schaus, S. E. Asymmetric Morita-Baylis-Hillman Reactions Catalyzed by Chiral Brønsted Acids. J. Am. Chem. Soc. 2003, 125, 12094-12095.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 12094-12095
-
-
Mcdougal, N.T.1
Schaus, S.E.2
-
125
-
-
49349113318
-
Asymmetric morita-baylis-hillman reaction of arylaldehydes with 2- cyclohexen-1-one catalyzed by chiral bis(thio)urea and dabco
-
Shi, M.; Liu, X.-G. Asymmetric Morita-Baylis-Hillman Reaction of Arylaldehydes with 2- Cyclohexen-1-one Catalyzed by Chiral Bis(Thio)urea and DABCO. Org. Lett. 2008, 10, 1043-1046.
-
(2008)
Org. Lett.
, vol.10
, pp. 1043-1046
-
-
Shi, M.1
Liu, X.-G.2
-
126
-
-
15744396095
-
Bifunctional organocatalysts for enantioselective aza-morita- baylis-hillman reaction
-
Matsui, K.; Takizawa, S.; Sasai. H. Bifunctional organocatalysts for enantioselective aza-Morita- Baylis-Hillman reaction. J. Am. Chem. Soc. 2005, 127, 3680-3681.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3680-3681
-
-
Matsui, K.1
Takizawa, S.2
Sasai, H.3
-
127
-
-
33645868666
-
Conformational lock in a brønsted acid-lewis base organocatalyst for the aza-morita-baylis-hillman reaction
-
Matsui, K.; Tanaka, K.; Horii, A.; Takizawa, S.; Sasai. H. Conformational lock in a Brønsted acid-Lewis base organocatalyst for the aza-Morita-Baylis-Hillman reaction. Tetrahedron: Asymmetry 2006, 17, 578-583.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 578-583
-
-
Matsui, K.1
Tanaka, K.2
Horii, A.3
Takizawa, S.4
Sasai., H.5
-
128
-
-
0038696449
-
Chiral phosphine lewis base catalyzed asymmetric aza-baylis-hillman reaction of n-sulfonated imines with methyl vinyl ketone and phenyl acrylate
-
Shi, M.; Chen. L.-H. Chiral phosphine Lewis base catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone and phenyl acrylate. Chem. Commun. 2003, 1310-1311.
-
(2003)
Chem. Commun.
, pp. 1310-1311
-
-
Shi, M.1
Chen., L.-H.2
-
129
-
-
28244436733
-
Asymmetric aza-morita-baylis-hillman reaction of nsulfonated imines with methyl vinyl ketone catalyzed by chiral phosphine lewis bases bearing perfluoroalkanes as pony tails
-
Shi, M.; Chen. L.-H.; Teng, W.D. Asymmetric aza-Morita-Baylis-Hillman reaction of Nsulfonated imines with methyl vinyl ketone catalyzed by chiral phosphine Lewis bases bearing perfluoroalkanes as pony tails. Adv. Synth. Catal. 2005, 347, 1781-1789.
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1781-1789
-
-
Shi, M.1
Chen., L.-H.2
Teng, W.D.3
-
130
-
-
27544493994
-
Catalytic asymmetric aza-baylis-hillman reaction of n-sulfonated imines with 2-cyclohexen-1-one and 2-cyclopenten-1-one in the presence of a chiral phosphine lewis base
-
Shi, M.; Li, C.Q. Catalytic, asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with 2-cyclohexen-1-one and 2-cyclopenten-1-one in the presence of a chiral phosphine Lewis base. Tetrahedron Asymmetry 2005, 16, 1385-1391.
-
(2005)
Tetrahedron Asymmetry
, vol.16
, pp. 1385-1391
-
-
Shi, M.1
Li, C.Q.2
-
131
-
-
33744818862
-
Asymmetric aza-morita-baylis-hillman reaction of nsulfonated imines with activated olefins catalyzed by chiral phosphine lewis bases bearing multiple phenol groups
-
Liu, Y.-H.; Chen, L.-C.; Shi, M. Asymmetric Aza-Morita-Baylis-Hillman Reaction of NSulfonated Imines with Activated Olefins Catalyzed by Chiral Phosphine Lewis Bases Bearing Multiple Phenol Groups. Adv. Synth. Catal. 2006, 348, 973-979.
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 973-979
-
-
Liu, Y.-H.1
Chen, L.-C.2
Shi, M.3
-
132
-
-
50649095554
-
Chiral sterically congested phosphane-amide bifunctional organocatalysts in asymmetric aza-morita-baylis-hillman reactions of n-sulfonated imines with methyl and ethyl vinyl ketones
-
Guan, X.- Y.; Jiang, Y.-Q.; Shi, M. Chiral Sterically Congested Phosphane-Amide Bifunctional Organocatalysts in Asymmetric Aza-Morita-Baylis- Hillman Reactions of N-Sulfonated Imines with Methyl and Ethyl Vinyl Ketones. Eur. J. Org. Chem. 2008, 2150-2155.
-
(2008)
Eur. J. Org. Chem.
, pp. 2150-2155
-
-
Guan, X.-Y.1
Jiang, Y.-Q.2
Shi, M.3
-
133
-
-
34547599687
-
Highly enantioselective aza-morita-baylis-hillman reaction with a bisphenol-based bifunctional organocatalyst
-
Ito, K.; Nishida, K.; Gotanda, T. Highly enantioselective aza-Morita-Baylis-Hillman reaction with a bisphenol-based bifunctional organocatalyst. Tetrahedron Lett. 2007, 48, 6147-6149.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 6147-6149
-
-
Ito, K.1
Nishida, K.2
Gotanda, T.3
-
134
-
-
0035801811
-
Assesing the scope of the tandem michael/intramolecular aldol reaction mediated by secondary amines, thiols and phosphines
-
Richards, E.L.; Murphy, P.J.; Dinon, F.; Fratucello, S.; Brown, P.M.; Gelbrich, T.; Hurstouse, M.B. Assesing the scope of the tandem Michael/intramolecular aldol reaction mediated by secondary amines, thiols and phosphines. Tetrahedron 2001, 57, 7771-7784.
-
(2001)
Tetrahedron
, vol.57
, pp. 7771-7784
-
-
Richards, E.L.1
Murphy, P.J.2
Dinon, F.3
Fratucello, S.4
Brown, P.M.5
Gelbrich, T.6
Hurstouse, M.B.7
-
135
-
-
0033574545
-
Tandem intramolecular/aldol reactions mediated by secondary amines, thiols and phosphines
-
Dinon, F.; Richards, E.; Murphy, P.J.; Hibbs, D.E.; Hurtshouse, M.B.; Abdul Malik, K.M. Tandem intramolecular/aldol reactions mediated by secondary amines, thiols and phosphines. Tetrahedron Lett. 1999, 40, 3279-3282.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 3279-3282
-
-
Dinon, F.1
Richards, E.2
Murphy, P.J.3
Hibbs, D.E.4
Hurtshouse, M.B.5
Abdul Malik, K.M.6
-
136
-
-
0030700308
-
Intramolecular baylis-hillman reaction catalyzed by secondary amines
-
Black, G.P.; Dinon, F.; Fratucello, S.; Murphy, P.J.; Nielsen, M.; Williams, H.L. Intramolecular Baylis-Hillman reaction catalyzed by secondary amines. Tetrahedron Lett. 1997, 38, 8561-8564.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 8561-8564
-
-
Black, G.P.1
Dinon, F.2
Fratucello, S.3
Murphy, P.J.4
Nielsen, M.5
Williams, H.L.6
-
137
-
-
0036134467
-
Lewis base and l-proline co-catalyzed baylis-hillman reaction of arylaldehydes with metil vinyl ketone
-
Shi, M.; Jiang, J.-K.; Li, C.-Q. Lewis base and L-proline co-catalyzed Baylis-Hillman reaction of arylaldehydes with metil vinyl ketone. Tetrahedron Lett. 2002, 43, 127-130.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 127-130
-
-
Shi, M.1
Jiang, J.-K.2
Li, C.-Q.3
-
138
-
-
0037048346
-
An exploration of asymmetric baylis-hillman reactions catalyzed by quinidine-derived chiral amines
-
Shi, M.; Jiang, J.-K. An exploration of asymmetric Baylis-Hillman reactions catalyzed by quinidine-derived chiral amines. Tetrahedron Asymmetry 2002, 13, 1941-1947.
-
(2002)
Tetrahedron Asymmetry
, vol.13
, pp. 1941-1947
-
-
Shi, M.1
Jiang, J.-K.2
-
139
-
-
0034654216
-
Proline-catalyzed direct asymmetric aldol reactions
-
List, B.; Lerner, R.; Barbas, C.F., III. Proline-catalyzed direct asymmetric aldol reactions. J. Am. Chem. Soc. 2000, 122, 2395-2396.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 2395-2396
-
-
List, B.1
Lerner, R.2
Barbas III, C.F.3
-
140
-
-
0034596299
-
Catalytic asymmetric synthesis of anti-1,2-diols
-
Notz, W.; List, B. Catalytic Asymmetric Synthesis of anti-1,2-diols. J. Am. Chem. Soc. 2000, 122, 7386-7387.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 7386-7387
-
-
Notz, W.1
List, B.2
-
141
-
-
0034596452
-
A proline-catalyzed asymmetric robinson annulation reaction
-
Bui, T.; Barbas, III, C.F., A proline-catalyzed asymmetric Robinson annulation reaction. Tetrahedron Lett. 2000, 41, 6951-6954.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 6951-6954
-
-
Bui, T.1
Barbas III, C.F.2
-
142
-
-
0034600250
-
New strategies for organic catalysis: The first highly enantioselective organocatalytic diels-alder reaction
-
Ahrendt, K.A.; Borths, C.J.; MacMillan, D.W.C. New strategies for organic catalysis: the First highly enantioselective organocatalytic Diels-Alder reaction. J. Am. Chem. Soc. 2000, 122, 4243-4244.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 4243-4244
-
-
Ahrendt, K.A.1
Borths, C.J.2
MacMillan, D.W.C.3
-
143
-
-
0037420321
-
Quantum-mechanical predictions of the stereoselectivities of proline-catalyzed asymmetric intermolecular aldol additions
-
Bahmanyar, S.; Houk, K.N.; Martin, H.J.; List, B. Quantum-mechanical predictions of the stereoselectivities of proline-catalyzed asymmetric intermolecular Aldol Additions. J. Am. Chem. Soc. 2003, 125, 2475-2479.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 2475-2479
-
-
Bahmanyar, S.1
Houk, K.N.2
Martin, H.J.3
List, B.4
-
144
-
-
34548691690
-
(1r2r)-(-)-2-dimethylamino-1-(4- nitrophenyl)-1,3-propanediol/l-proline cocatalyzed enantioselective morita-baylis-hillman reaction
-
Tang, H.; Gao, P.; Zhao, G.; Zhou, Z.; He, L.; Tang, C. (1R,2R)-(-)-2-Dimethylamino-1-(4- nitrophenyl)-1,3-propanediol/L-proline cocatalyzed enantioselective Morita-Baylis-Hillman reaction. Cat. Commun. 2007, 8, 1811-1814.
-
(2007)
Cat. Commun.
, vol.8
, pp. 1811-1814
-
-
Tang, H.1
Gao, P.2
Zhao, G.3
Zhou, Z.4
He, L.5
Tang, C.6
-
145
-
-
38049086667
-
Chiral tertiary amine/l-proline cocatalyzed enantioselective morita-baylis-hillman (MBH) reaction
-
Tang, H.; Zhao, G.; Zhou, Z.; Gao, P.; He, L.; Tang, C. Chiral tertiary Amine/L-Proline Cocatalyzed Enantioselective Morita-Baylis-Hillman (MBH) Reaction. Eur. J. Org. Chem. 2008, 126-135.
-
(2008)
Eur. J. Org. Chem.
, pp. 126-135
-
-
Tang, H.1
Zhao, G.2
Zhou, Z.3
Gao, P.4
He, L.5
Tang, C.6
-
146
-
-
0142042898
-
Dual catalyst control in the amino acid-peptidecatalyzed enantioselective baylis-hillman reaction
-
Imbriglio, J.E.; Vasbinder, M.M.; Miller, S.J. Dual catalyst control in the amino acid-peptidecatalyzed enantioselective Baylis-Hillman Reaction. Org. Lett. 2003, 5, 3741-3743.
-
(2003)
Org. Lett.
, vol.5
, pp. 3741-3743
-
-
Imbriglio, J.E.1
Vasbinder, M.M.2
Miller, S.J.3
-
147
-
-
33750437400
-
Amino acid-peptide-catalyzed enantioselective morita-baylis-hillman reactions
-
Vasbinder, M.M.; Imbriglio, J.E.; Miller, S.J. Amino acid-peptide- catalyzed enantioselective Morita-Baylis-Hillman reactions. Tetrahedron 2006, 62, 11450-11459.
-
(2006)
Tetrahedron
, vol.62
, pp. 11450-11459
-
-
Vasbinder, M.M.1
Imbriglio, J.E.2
Miller, S.J.3
-
148
-
-
24944559389
-
Dual catalyst control in the enantioselective intramolecular morita-baylis-hillman reaction
-
Aroyan, C.E.; Vasbinder, M.M.; Miller, S.J. Dual Catalyst Control in the Enantioselective Intramolecular Morita-Baylis-Hillman Reaction. Org. Lett. 2005, 7, 3849-3851.
-
(2005)
Org. Lett.
, vol.7
, pp. 3849-3851
-
-
Aroyan, C.E.1
Vasbinder, M.M.2
Miller, S.J.3
-
149
-
-
27944479071
-
AN Unexpected Inversion Of Enantioselectivity In The Proline Catalyzed Intramolecular Baylis-Hillman Reaction
-
Chen, S.-H.; Hong, B.-C.; Su, C.-F.; Sarshar, S. An unexpected inversion of enantioselectivity in the proline catalyzed intramolecular Baylis-Hillman reaction. Tetrahedron Lett. 2005, 46, 8899-8903.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8899-8903
-
-
Chen, S.-H.1
Hong, B.-C.2
Su, C.-F.3
Sarshar, S.4
-
150
-
-
8844256133
-
COmputational Evidence For The Enamine Mechanism Of Intramolecular Aldol Reactions Catalyzed By Proline
-
Clemente, F.R.; Houk, K.N. Computational evidence for the enamine mechanism of intramolecular Aldol Reactions catalyzed by proline. Angew. Chem. Int. Ed. 2004, 43, 5766-5768.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5766-5768
-
-
Clemente, F.R.1
Houk, K.N.2
-
151
-
-
23844543306
-
Theoretical studies of stereoselectivities of intramolecular aldol cyclizations catalyzed by amino acids
-
Clemente, F.R.; Houk, K.N. Theoretical Studies of Stereoselectivities of Intramolecular Aldol Cyclizations Catalyzed by Amino Acids. J. Am. Chem. Soc. 2005, 127, 11294-11302.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 11294-11302
-
-
Clemente, F.R.1
Houk, K.N.2
-
152
-
-
60749108597
-
A. density functional study of proline- catalyzed intramolecular baylis-hillman reactions
-
Duarte, F.J.S.; Cabrita, E.J.; Frenking, G.; Gil Santos, A. Density Functional Study of Proline- Catalyzed Intramolecular Baylis-Hillman Reactions. Chem. Eur. J. 2009, 15, 1734-1746.
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 1734-1746
-
-
Duarte, F.J.S.1
Cabrita, E.J.2
Frenking, G.3
Gil, S.4
-
153
-
-
0038729533
-
Direct catalytic asymmetric eno/exo aldolizations
-
Pidathala, C.; Hoang, L.; Vignola, N.; List, B. Direct, Catalytic Asymmetric eno/exo Aldolizations. Angew. Chem. Int. Ed. 2003, 42, 2785-2788.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 2785-2788
-
-
Pidathala, C.1
Hoang, L.2
Vignola, N.3
List, B.4
-
154
-
-
34249712553
-
A way to highly enantiomerically enriched aza-morita-baylis-hillman-type products
-
Utsumi, N.; Zhang, H.; Tanaka, F.; Barbas, III, C.F. A Way to highly enantiomerically enriched Aza-Morita-Baylis-Hillman-type products. Angew. Chem. Int. Ed. 2007, 46, 1878-1880.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 1878-1880
-
-
Utsumi, N.1
Zhang, H.2
Tanaka, F.3
Barbas III, C.F.4
-
155
-
-
34548249167
-
Aza-morita-baylis-hillman-type reactions: Highly enantioselective organocatalytic addition of unmodified a,β-unsaturated aldehydes to n-boc protected imines
-
Vesely, J.; Dziedzic, P.; Csrdova, A. Aza-Morita-Baylis-Hillman-type reactions: highly enantioselective organocatalytic addition of unmodified a,β-unsaturated aldehydes to N-BOC protected imines. Tetrahedron Lett. 2007, 48, 6900-6904.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 6900-6904
-
-
Vesely, J.1
Dziedzic, P.2
Córdova, A.3
-
156
-
-
0034721440
-
The direct catalytic asymmetric three-component mannich reaction
-
List, B. the direct catalytic asymmetric three-component mannich reaction. J. Am. Chem. Soc. 2000, 126, 9336-9337.
-
(2000)
J. Am. Chem. Soc.
, vol.126
, pp. 9336-9337
-
-
List, B.1
-
157
-
-
0037028550
-
The proline-catalized asymmetric three component mannich reaction: Scope, optimization, and applications to the highly enbantioselective synthesis of 1,2-aminoalcohols
-
List, B.; Pojarliev, P.; Biller, W.T.; Martin, H.J. The proline-catalized asymmetric three component Mannich reaction: Scope, optimization, and applications to the highly enbantioselective synthesis of 1,2-aminoalcohols. J. Am. Chem. Soc. 2002, 124, 827-833.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 827-833
-
-
List, B.1
Pojarliev, P.2
Biller, W.T.3
Martin, H.J.4
-
158
-
-
33746298422
-
Highly enantioselective aza-baylis-hillman in a chiral reaction medium
-
Gausepohl, R.; Buskens, P.; Kleinen, J.; Bruckman, A. ; Lehmann, C.W.; Klankermayer, J.; Leitner, W. Highly enantioselective Aza-Baylis-Hillman in a chiral reaction medium. Angew. Chem. Int. Ed. 2006, 45, 3689-3692.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 3689-3692
-
-
Gausepohl, R.1
Buskens, P.2
Kleinen, J.3
Bruckman, A.4
Lehmann, C.W.5
Klankermayer, J.6
Leitner, W.7
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