-
1
-
-
79952352647
-
Organocatalytic enantioselective β-functionalization of aldehydes via oxidation of enamines and their application in cascade reactions
-
10.1038/ncomms1214
-
S.L. Zhang H.X. Xie J. Zhu H. Li X.S. Zhang J. Li W. Wang 2011 Organocatalytic enantioselective β-functionalization of aldehydes via oxidation of enamines and their application in cascade reactions Nature Commun 2 211 10.1038/ncomms1214
-
(2011)
Nature Commun
, vol.2
, pp. 211
-
-
Zhang, S.L.1
Xie, H.X.2
Zhu, J.3
Li, H.4
Zhang, X.S.5
Li, J.6
Wang, W.7
-
2
-
-
79954614511
-
Oxidative and enantioselective cross-coupling of aldehydes and nitromethane catalyzed by diphenylprolinol silyl ether
-
10.1002/anie.201006885 1:CAS:528:DC%2BC3MXkslCiu7Y%3D
-
Y. Hayashi T. Itoh H. Ishikawa 2011 Oxidative and enantioselective cross-coupling of aldehydes and nitromethane catalyzed by diphenylprolinol silyl ether Angew Chem Int Ed 50 17 3920 3924 10.1002/anie.201006885 1:CAS:528:DC%2BC3MXkslCiu7Y%3D
-
(2011)
Angew Chem Int Ed
, vol.50
, Issue.17
, pp. 3920-3924
-
-
Hayashi, Y.1
Itoh, T.2
Ishikawa, H.3
-
4
-
-
67549134370
-
2 co-catalyzed Saegusa oxidation reaction of unmodified aldehydes to alpha, beta-unsaturated aldehydes
-
10.1002/adsc.200900011 1:CAS:528:DC%2BD1MXos1arur8%3D
-
2 co-catalyzed Saegusa oxidation reaction of unmodified aldehydes to alpha, beta-unsaturated aldehydes Adv Synth Catal 351 9 1229 1232 10.1002/adsc.200900011 1:CAS:528:DC%2BD1MXos1arur8%3D
-
(2009)
Adv Synth Catal
, vol.351
, Issue.9
, pp. 1229-1232
-
-
Zhu, J.1
Liu, J.2
Ma, R.3
Xie, H.X.4
Li, J.5
Jiang, H.L.6
Wang, W.7
-
5
-
-
0034600250
-
New strategies for organic catalysis: The first highly enantioselective organocatalytic diels - Alder reaction [16]
-
DOI 10.1021/ja000092s
-
K.A. Ahrendt C.J. Borths D.W.C. MacMillan 2000 New strategies for organic catalysis: the first highly enantioselective organocatalytic Diels-Alder reaction J Am Chem Soc 122 17 4243 4244 10.1021/ja000092s 1:CAS:528: DC%2BD3cXisVGjurw%3D (Pubitemid 30304872)
-
(2000)
Journal of the American Chemical Society
, vol.122
, Issue.17
, pp. 4243-4244
-
-
Ahrendt, K.A.1
Borths, C.J.2
MacMillan, D.W.C.3
-
6
-
-
33745715054
-
Modern strategies in organic catalysis: The advent and development of iminium activation
-
G. Lelais D.W.C. MacMillan 2006 Modern strategies in organic catalysis: the advent and development of iminium activation Aldrichimica Acta 39 3 79 87 1:CAS:528:DC%2BD28XmsF2kt7g%3D (Pubitemid 43999074)
-
(2006)
Aldrichimica Acta
, vol.39
, Issue.3
, pp. 79-87
-
-
Lelais, G.1
MacMillan, D.W.C.2
-
7
-
-
38349178582
-
Iminium catalysis
-
10.1021/cr068388p
-
A. Erkkilä I. Majander P.M. Pihko 2007 Iminium catalysis Chem Rev 107 12 5416 5470 10.1021/cr068388p
-
(2007)
Chem Rev
, vol.107
, Issue.12
, pp. 5416-5470
-
-
Erkkilä, A.1
Majander, I.2
Pihko, P.M.3
-
8
-
-
0038824420
-
An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides
-
DOI 10.1021/ol034071p
-
G. Battistuzzi S. Cacchi G. Fabrizi 2003 An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides Org Lett 5 5 777 780 10.1021/ol034071p 1:CAS:528:DC%2BD3sXhtFSgtro%3D (Pubitemid 37141101)
-
(2003)
Organic Letters
, vol.5
, Issue.5
, pp. 777-780
-
-
Battistuzzi, G.1
Cacchi, S.2
Fabrizi, G.3
-
10
-
-
85083263815
-
The Peterson reaction
-
Peterson olefinations
-
Peterson olefinations: (c) Ager DJ. The Peterson reaction. Synthesis, 1984, (5): 384-398
-
(1984)
Synthesis
, Issue.5
, pp. 384-398
-
-
Ager, D.J.1
-
11
-
-
0037393960
-
Synthetic aspects of stereoselective hydroformylation
-
10.1021/ar0200596 1:CAS:528:DC%2BD3sXmslersg%3D%3D
-
B. Breit 2003 Synthetic aspects of stereoselective hydroformylation Acc Chem Res 36 4 264 275 10.1021/ar0200596 1:CAS:528:DC%2BD3sXmslersg%3D%3D
-
(2003)
Acc Chem Res
, vol.36
, Issue.4
, pp. 264-275
-
-
Breit, B.1
-
12
-
-
53549118624
-
Palladium catalysts for the formylation of vinyl triflates to form α,β-unsaturated aldehydes
-
10.1002/anie.200800994 1:CAS:528:DC%2BD1cXotVSltbY%3D
-
H. Neumann A. Sergeev M. Beller 2008 Palladium catalysts for the formylation of vinyl triflates to form α,β-unsaturated aldehydes Angew Chem Int Ed 47 26 4887 4891 10.1002/anie.200800994 1:CAS:528: DC%2BD1cXotVSltbY%3D
-
(2008)
Angew Chem Int Ed
, vol.47
, Issue.26
, pp. 4887-4891
-
-
Neumann, H.1
Sergeev, A.2
Beller, M.3
-
13
-
-
0032500326
-
Asymmetric total synthesis of callystatin A: Asymmetric aldol additions with titanium enolates of acyloxazolidinethiones [8]
-
DOI 10.1021/ja9817500
-
M.T. Crimmins B.W. King 1998 Asymmetric total synthesis of callystatin A: Asymmetric aldol additions with titanium enolates of acyloxazolidinethiones J Am Chem Soc 120 35 9084 9085 10.1021/ja9817500 1:CAS:528:DyaK1cXlt1SmsLk%3D (Pubitemid 28449196)
-
(1998)
Journal of the American Chemical Society
, vol.120
, Issue.35
, pp. 9084-9085
-
-
Crimmins, M.T.1
King, B.W.2
-
14
-
-
48549105711
-
-
A.R. Katritzky R.J.K. Taylor S. Jone (eds). Elsevier Dordrecht
-
Cross-aldol condensations: (g) Mackie PR, Foster CE. in Comprehensive Organic Group Transformations II, Vol. 3 (Eds. Katritzky AR, Taylor RJK, Jone S), Elsevier, Dordrecht, 2004. 59
-
(2004)
Comprehensive Organic Group Transformations II, Vol. 3
, pp. 59
-
-
MacKie, P.R.1
Foster, C.E.2
-
15
-
-
0001848341
-
The Wittig olefination reaction and modifications involving selected synthetic aspects phosphoryl-stabilized carbanions. Stereochemistry
-
10.1021/cr00094a007 1:CAS:528:DyaL1MXktVKmsb4%3D
-
B.E. Maryanoff A.B. Reitz 1989 The Wittig olefination reaction and modifications involving selected synthetic aspects phosphoryl-stabilized carbanions. Stereochemistry Chem Rev 89 4 863 972 10.1021/cr00094a007 1:CAS:528:DyaL1MXktVKmsb4%3D
-
(1989)
Chem Rev
, vol.89
, Issue.4
, pp. 863-972
-
-
Maryanoff, B.E.1
Reitz, A.B.2
-
17
-
-
79851503103
-
2-Iodoxybenzoic acid: A simple oxidant with a dazzling array of potential applications
-
10.1002/anie.201000873 1:CAS:528:DC%2BC3MXhslygtrw%3D
-
A. Duschek S.F. Kirsch 2011 2-Iodoxybenzoic acid: A simple oxidant with a dazzling array of potential applications Angew Chem Int Ed 50 7 1524 1552 10.1002/anie.201000873 1:CAS:528:DC%2BC3MXhslygtrw%3D
-
(2011)
Angew Chem Int Ed
, vol.50
, Issue.7
, pp. 1524-1552
-
-
Duschek, A.1
Kirsch, S.F.2
-
18
-
-
77956385744
-
2-Iodoxybenzoic acid (IBX): An efficient hypervalent iodine reagent
-
10.1016/j.tet.2010.07.014 1:CAS:528:DC%2BC3cXhtV2itrfK
-
V. Satam A. Harad R. Rajule H. Pati 2010 2-Iodoxybenzoic acid (IBX): An efficient hypervalent iodine reagent Tetrahedron 66 39 7659 7706 10.1016/j.tet.2010.07.014 1:CAS:528:DC%2BC3cXhtV2itrfK
-
(2010)
Tetrahedron
, vol.66
, Issue.39
, pp. 7659-7706
-
-
Satam, V.1
Harad, A.2
Rajule, R.3
Pati, H.4
-
19
-
-
64549092935
-
Hypervalent iodine-mediated oxidation of alcohols
-
10.1039/b823399c
-
M. Uyanik K. Ishihara 2009 Hypervalent iodine-mediated oxidation of alcohols Chem Commun 16 2086 2099 10.1039/b823399c
-
(2009)
Chem Commun
, vol.16
, pp. 2086-2099
-
-
Uyanik, M.1
Ishihara, K.2
-
20
-
-
1942439120
-
Hypervalent iodine reagents for the oxidation of alcohols and their application to complex molecule synthesis
-
H. Tohma Y. Kita 2004 Hypervalent iodine reagents for the oxidation of alcohols and their application to complex molecule synthesis Adv Synth Catal 346 2-3 111 124 10.1002/adsc.200303203 1:CAS:528:DC%2BD2cXjt1ensLY%3D (Pubitemid 38515549)
-
(2004)
Advanced Synthesis and Catalysis
, vol.346
, Issue.2-3
, pp. 111-124
-
-
Tohma, H.1
Kita, Y.2
-
21
-
-
0035800351
-
IBX - New reactions with an old reagent
-
DOI 10.1002/1521-3773(20010803)40:15<2812::AID-ANIE2812>3.0.CO;2-X
-
T. Wirth 2001 IBX-New reactions with an old reagent Angew Chem Int Ed 40 15 2812 2814 10.1002/1521-3773(20010803)40:15<2812::AID-ANIE2812>3.0.CO;2- X 1:CAS:528:DC%2BD3MXmt1Wmu7o%3D (Pubitemid 32783350)
-
(2001)
Angewandte Chemie - International Edition
, vol.40
, Issue.15
, pp. 2812-2814
-
-
Wirth, T.1
-
22
-
-
51749084445
-
α,α-Diarylprolinol ethers: New tools for functionalization of carbonyl compounds
-
10.1002/asia.200700417 1:CAS:528:DC%2BD1cXnsVGlsLY%3D
-
A. Mielgo C. Palomo 2008 α,α-Diarylprolinol ethers: new tools for functionalization of carbonyl compounds Chem Asian J 3 6 922 948 10.1002/asia.200700417 1:CAS:528:DC%2BD1cXnsVGlsLY%3D
-
(2008)
Chem Asian J
, vol.3
, Issue.6
, pp. 922-948
-
-
Mielgo, A.1
Palomo, C.2
-
24
-
-
22144459070
-
Diphenylprolinol silyl ethers as efficient organocatalysts for the asymmetric Michael reaction of aldehydes and nitroalkenes
-
DOI 10.1002/anie.200500599
-
Y. Hayashi H. Gotoh T. Hayashi M. Shoji 2005 Diphenylprolinol silyl ethers as efficient organocatalysts for the asymmetric Michael reaction of aldehydes and nitroalkenes Angew Chem Int Ed 44 18 4212 4215 10.1002/anie.200500599 1:CAS:528:DC%2BD2MXmsVartbg%3D (Pubitemid 40968498)
-
(2005)
Angewandte Chemie - International Edition
, vol.44
, Issue.27
, pp. 4212-4215
-
-
Hayashi, Y.1
Gotoh, H.2
Hayashi, T.3
Shoji, M.4
-
25
-
-
25444470782
-
Diphenylprolinol methyl ether: A highly enantioselective catalyst for Michael addition of aldehydes to simple enones
-
DOI 10.1021/ol0517729
-
Y. Chi S.H. Gellman 2005 Diphenylprolinol methyl ether: A highly enantioselective catalyst for Michael addition of aldehydes to simple enones Org Lett 7 19 4253 4256 10.1021/ol0517729 1:CAS:528:DC%2BD2MXotVSlu7k%3D (Pubitemid 41361576)
-
(2005)
Organic Letters
, vol.7
, Issue.19
, pp. 4253-4256
-
-
Chi, Y.1
Gellman, S.H.2
-
26
-
-
0037070535
-
Iodine(V) reagents in organic synthesis. Part 4. o-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes
-
DOI 10.1021/ja012127+
-
K.C. Nicolaou T. Montagnon P.S. Baran Y.L. Zhong 2002 Iodine (V) reagents in organic synthesis. Part 4. o-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes J Am Chem Soc 124 10 2245 2258 10.1021/ja012127+ 1:CAS:528:DC%2BD38Xht1eks7s%3D (Pubitemid 34267110)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.10
, pp. 2245-2258
-
-
Nicolaou, K.C.1
Montagnon, T.2
Baran, P.S.3
Zhong, Y.-L.4
-
27
-
-
0037087704
-
Modulation of the reactivity profile of IBX by ligand complexation: Ambient temperature dehydrogenation of aldehydes and ketones to α,β-unsaturated carbonyl compounds
-
DOI 10.1002/1521-3773(20020315)41:6<993::AID-ANIE993>3.0.CO;2-U
-
K.C. Nicolaou T. Montagnon P.S. Baran 2002 Modulation of the reactivity profile of IBX by ligand complexation: Ambient temperature dehydration of aldehydes and ketones to α,β-unsaturated carbonyls Angew Chem Int Ed 41 6 993 996 10.1002/1521-3773(20020315)41:6<993::AID-ANIE993>3.0.CO;2-U 1:CAS:528:DC%2BD38XisVejs7s%3D (Pubitemid 34251893)
-
(2002)
Angewandte Chemie - International Edition
, vol.41
, Issue.6
, pp. 993-996
-
-
Nicolaou, K.C.1
Montagnon, T.2
Baran, P.S.3
|