-
1
-
-
0003799267
-
-
Stang, P. J., Diederich, F., Eds. VCH: Weinheim, Germany
-
Modern Acetylene Chemistry; Stang, P. J., Diederich, F., Eds.; VCH: Weinheim, Germany, 1995.
-
(1995)
Modern Acetylene Chemistry
-
-
-
2
-
-
66149109902
-
The enantioselective addition of alkyne nucleophiles to carbonyl groups
-
For an excellent review on the subject, see
-
For an excellent review on the subject, see: Trost, B. M.; Weiss, A. H. The enantioselective addition of alkyne nucleophiles to carbonyl groups Adv. Synth. Catal. 2009, 351, 963-983
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 963-983
-
-
Trost, B.M.1
Weiss, A.H.2
-
3
-
-
33750309194
-
Atom economy - A challenge for organic synthesis: Homogeneous catalysis leads the way
-
Trost, B. M. Atom economy-A challenge for organic synthesis: Homogeneous catalysis leads the way Angew. Chem., Int. Ed. Engl. 1995, 34, 259-281
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 259-281
-
-
Trost, B.M.1
-
4
-
-
0026418434
-
The atom economy: A search for synthetic efficiency
-
Trost, B. M. The atom economy: A search for synthetic efficiency Science 1991, 254, 1471-1477
-
(1991)
Science
, vol.254
, pp. 1471-1477
-
-
Trost, B.M.1
-
6
-
-
0031046817
-
Palladium-catalyzed additions of terminal alkynes to acceptor alkynes
-
DOI 10.1021/ja9624937, PII S0002786396024936
-
Trost, B. M.; Sorum, M. T.; Chan, C.; Harms, A. E.; Ruhter, G. Palladium-catalyzed additions of terminal alkynes to acceptor alkynes J. Am. Chem. Soc. 1997, 119, 698-708 (Pubitemid 27101233)
-
(1997)
Journal of the American Chemical Society
, vol.119
, Issue.4
, pp. 698-708
-
-
Trost, B.M.1
Sorum, M.T.2
Chan, C.3
Harms, A.E.4
Ruhter, G.5
-
7
-
-
70349988546
-
Asymmetric synthesis of β-alkynyl aldehydes by rhodium-catalyzed conjugate alkynylation
-
Nishimura, T.; Sawano, T.; Hayashi, T. Asymmetric Synthesis of β-Alkynyl Aldehydes by Rhodium-Catalyzed Conjugate Alkynylation Angew. Chem. Int. Ed. 2009, 48, 8057-8059
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 8057-8059
-
-
Nishimura, T.1
Sawano, T.2
Hayashi, T.3
-
8
-
-
33751500689
-
Tin ditriflate-promoted addition of 1-alkynes to aldehydes
-
Yamaguchi, M.; Hayashi, A.; Minami, T. Tin ditriflate-promoted addition of 1-alkynes to aldehydes J. Org. Chem. 1991, 56, 4091-4902
-
(1991)
J. Org. Chem.
, vol.56
, pp. 4091-4902
-
-
Yamaguchi, M.1
Hayashi, A.2
Minami, T.3
-
11
-
-
0029089453
-
Copper-catalyzed reaction of terminal alkynes with nitrones: Selective synthesis of 1-aza-1-buten-3-yne and 2-azetidinone derivatives
-
Miura, M.; Enna, M.; Okuro, K.; Nomura, M. Copper-catalyzed reaction of terminal alkynes with nitrones: Selective synthesis of 1-aza-1-buten-3-yne and 2-azetidinone derivatives J. Org. Chem. 1995, 60, 4999-5004
-
(1995)
J. Org. Chem.
, vol.60
, pp. 4999-5004
-
-
Miura, M.1
Enna, M.2
Okuro, K.3
Nomura, M.4
-
12
-
-
0033537047
-
Catalytic in situ generation of Zn(II)-alkynilides under mild conditions: A novel C - N addition process utilizing terminal acetylenes
-
Frantz, D. E.; Fässler, R.; Carreira, E. M. Catalytic in situ generation of Zn(II)-alkynilides under mild conditions: a novel C - N addition process utilizing terminal acetylenes J. Am. Chem. Soc. 1999, 121, 11245-11246
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 11245-11246
-
-
Frantz, D.E.1
Fässler, R.2
Carreira, E.M.3
-
13
-
-
3943075750
-
3-coupling (asymmetric aldehyde-alkyne-amine)
-
3-coupling (asymmetric aldehyde-alkyne-amine) Synlett 2004, 1472-1483
-
(2004)
Synlett
, pp. 1472-1483
-
-
Wei, C.1
Li, Z.2
Li, C.-J.3
-
14
-
-
33750167114
-
Direct addition of alkynes to imines and related C=N electrophiles: A convenient access to propargylamines
-
DOI 10.1039/b607986p
-
Zani, L.; Bolm, C. Direct addition of alkynes to imines and related C - N electrophiles: A convenient access to propargylamine Chem. Commun. 2006, 4263-4275 (Pubitemid 44596193)
-
(2006)
Chemical Communications
, Issue.41
, pp. 4263-4275
-
-
Zani, L.1
Bolm, C.2
-
15
-
-
0029975056
-
Aqueous barbier-grignard type reactions: Scope, mechanism and synthetic applications
-
Li, C.-J. Aqueous Barbier-Grignard type reactions: Scope, mechanism and synthetic applications Tetrahedron 1996, 52, 5643-5668
-
(1996)
Tetrahedron
, vol.52
, pp. 5643-5668
-
-
Li, C.-J.1
-
16
-
-
0032500322
-
Unexpected Barbier-Grignard allylation of aldehydes with magnesium in water
-
Li, C.-J.; Zhang, W.-C. Unexpected Barbier-Grignard allylation of aldehydes with magnesium in water J. Am. Chem. Soc. 1998, 120, 9102-9103
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 9102-9103
-
-
Li, C.-J.1
Zhang, W.-C.2
-
17
-
-
0002708983
-
In aqua synthesis of a high molecular weight poly(areneethylene) polymer with reversible hydrogel properties
-
Li, C.-J.; Slaven, W. T., IV.; Chen, Y. P.; John, V. T.; Rachakonda, S. H. In aqua synthesis of a high molecular weight poly(areneethylene) polymer with reversible hydrogel properties Chem. Commun. 1998, 1351-1352
-
(1998)
Chem. Commun.
, pp. 1351-1352
-
-
Li, C.-J.1
Slaven, W.T.I.V.2
Chen, Y.P.3
John, V.T.4
Rachakonda, S.H.5
-
19
-
-
0033543497
-
Organic syntheses using indium-mediated and catalyzed reactions in aqueous media
-
Li, C.-J.; Chan, T. H. Organic syntheses using indium-mediated and catalyzed reactions in aqueous media Tetrahedron 1999, 55, 11149-11176
-
(1999)
Tetrahedron
, vol.55
, pp. 11149-11176
-
-
Li, C.-J.1
Chan, T.H.2
-
20
-
-
57249097715
-
Grignard-type reaction via C-H activation in water
-
Wei, C.; Li, C.-J. Grignard-type reaction via C-H activation in water Green Chem. 2002, 4, 39-41
-
(2002)
Green Chem.
, vol.4
, pp. 39-41
-
-
Wei, C.1
Li, C.-J.2
-
21
-
-
0000860028
-
First evidence for the use of organosilver compounds in Pd-catalyzed coupling reactions: A mechanistic rationale for the Pd/Ag-catalyzed enyne synthesis?
-
DOI 10.1021/ol015830b
-
It was widely accepted prior to our studies that metal acetylides from group IB fail to participate in nucleophilic C - O addition, and in most cases, silver acetylide was utilized as a stoichiometric reagent only. Dillinger, S.; Bertus, P.; Pale, P. First evidence for the use of organosilver compounds in Pd-catalyzed coupling reactions: A mechanistic rationale for the Pd/Ag-catalyzed enyne synthesis? Org. Lett. 2001, 3, 1661-1664 (Pubitemid 33631659)
-
(2001)
Organic Letters
, vol.3
, Issue.11
, pp. 1661-1664
-
-
Dillinger, S.1
Bertus, P.2
Pale, P.3
-
22
-
-
26444461420
-
Phosphine-triggered complete chemo-switch: From efficient aldehyde-alkyne-amine coupling to efficient aldehyde-alkyne coupling in water
-
DOI 10.1021/ol051575+
-
Yao, X.; Li, C.-J. Phosphine-triggered complete chemo-switch: From efficient aldehyde-alkyne-amine coupling to efficient aldehyde-alkyne coupling in water Org. Lett. 2005, 7, 4395-4398 (Pubitemid 41436655)
-
(2005)
Organic Letters
, vol.7
, Issue.20
, pp. 4395-4398
-
-
Yao, X.1
Li, C.-J.2
-
23
-
-
0345687480
-
Aurones: A subclass of flavones with promising biological potential
-
DOI 10.2174/0929867033456468
-
For a review, see: Boumendjel, A. Aurones: A subclass of flavones with promising biological potential Curr. Med. Chem. 2003, 10, 2621-2630 (Pubitemid 37456031)
-
(2003)
Current Medicinal Chemistry
, vol.10
, Issue.23
, pp. 2621-2630
-
-
Boumendjel, A.1
-
24
-
-
0010501503
-
A novel oxidative cyclization of 2′-hydroxychalcones to 4,5-dialkoxyaurones by thallium(iii) nitrate
-
For an example, see
-
For an example, see: Thakkar, K.; Cushman, M. A novel oxidative cyclization of 2'-hydroxychalcones to 4,5-dialkoxyaurones by thallium(iii) nitrate J. Org. Chem. 1995, 60, 6499-6510
-
(1995)
J. Org. Chem.
, vol.60
, pp. 6499-6510
-
-
Thakkar, K.1
Cushman, M.2
-
25
-
-
39349098969
-
I- catalyzed cyclization
-
DOI 10.1021/jo702197b
-
Harkat, H.; Blanc, A.; Weibel, J.-M.; Pale, P. Versatile and expeditious synthesis of aurones via AuI-catalyzed cyclization J. Org. Chem. 2008, 73, 1620-1623 (Pubitemid 351263689)
-
(2008)
Journal of Organic Chemistry
, vol.73
, Issue.4
, pp. 1620-1623
-
-
Harkat, H.1
Blanc, A.2
Weibel, J.-M.3
Pale, P.4
-
26
-
-
66449090967
-
Water-triggered, counter anion-controlled and silver-phosphines complex catalyzed stereoselective cascade alkynylation-cyclization of terminal alkynes with salicylaldehydes
-
Yu, M.; Skouta, R.; Zhou, L.; Jiang, H.-F.; Yao, X.; Li, C.-J. Water-triggered, counter anion-controlled and silver-phosphines complex catalyzed stereoselective cascade alkynylation-cyclization of terminal alkynes with salicylaldehydes J. Org. Chem. 2009, 74, 3378-3383
-
(2009)
J. Org. Chem.
, vol.74
, pp. 3378-3383
-
-
Yu, M.1
Skouta, R.2
Zhou, L.3
Jiang, H.-F.4
Yao, X.5
Li, C.-J.6
-
27
-
-
33646447353
-
Water-triggered and gold(I)-catalyzed cascade addition/cyclization of terminal alkynes with ortho-alkynylaryl aldehyde
-
DOI 10.1021/ol060645p
-
Yao, X.; Li, C.-J. Water-triggered and gold-catalyzed cascade addition/cyclization of terminal alkynes with ortho-alkynylaryl aldehyde Org. Lett. 2006, 8, 1953-1955 (Pubitemid 43692198)
-
(2006)
Organic Letters
, vol.8
, Issue.9
, pp. 1953-1955
-
-
Yao, X.1
Li, C.-J.2
-
28
-
-
27744595601
-
The catalysis gold rush: New claims
-
For a review, see
-
For a review, see: Hashmi, A. S. K. The catalysis gold rush: New claims Angew. Chem., Int. Ed. 2005, 44, 6990-6993
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 6990-6993
-
-
Hashmi, A.S.K.1
-
29
-
-
0037170103
-
A highly stereoselective, novel coupling reaction between alkynes with aldehydes
-
Viswanathan, G. S.; Li, C.-J. A highly stereoselective, novel coupling reaction between alkynes with aldehydes Tetrahedron Lett. 2002, 43, 1613-1615
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 1613-1615
-
-
Viswanathan, G.S.1
Li, C.-J.2
-
30
-
-
4544240451
-
A remarkably efficient coupling of acid chlorides with alkynes in water
-
DOI 10.1021/ol048789w
-
Chen, L.; Li, C.-J. A remarkably efficient coupling of acid chlorides with alkynes in water Org. Lett. 2004, 6, 3151-3153 (Pubitemid 39233142)
-
(2004)
Organic Letters
, vol.6
, Issue.18
, pp. 3151-3153
-
-
Chen, L.1
Li, C.-J.2
-
32
-
-
46449110551
-
Efficient direct alkynylation of trifluoromethyl ketones catalyzed by agf in water and organic solvents
-
DOI 10.1055/s-2008-1078421
-
Deng, G.; Li, C.-J. Efficient direct alkynylation of trifluoromethyl ketones catalyzed by AgF in water and organic solvents Synlett 2008, 1571-1573 (Pubitemid 351930820)
-
(2008)
Synlett
, Issue.10
, pp. 1571-1573
-
-
Deng, G.J.1
Li, C.J.2
-
33
-
-
34547936758
-
Copper(I) alkoxide-catalyzed alkynylation of trifluoromethyl ketones
-
Motoki, R.; Kanai, M.; Shibasaki, M. Copper(I) alkoxide-catalyzed alkynylation of trifluoromethyl ketones Org. Lett. 2007, 9, 2997-3000
-
(2007)
Org. Lett.
, vol.9
, pp. 2997-3000
-
-
Motoki, R.1
Kanai, M.2
Shibasaki, M.3
-
34
-
-
0037034081
-
Highly efficient Grignard-type imine additions via C-H activation in water and under solvent-free conditions
-
Li, C.-J.; Wei, C. Highly efficient Grignard-type imine additions via C-H activation in water and under solvent-free conditions Chem. Commun. 2002, 268-269 (Pubitemid 34146482)
-
(2002)
Chemical Communications
, Issue.3
, pp. 268-269
-
-
Li, C.-J.1
Wei, C.2
-
35
-
-
0035796754
-
A three-component coupling reaction of aldehydes, amines, and alkynes
-
DOI 10.1002/1521-3773(20010702)40:13<2534::AID-ANIE2534>3.0.CO;2-2
-
Satoshi, S.; Takashi, K.; Ishii, Y. A three-component coupling reaction of aldehydes, amines, and alkynes Angew. Chem., Int. Ed. 2001, 40, 2534-2536 (Pubitemid 32645739)
-
(2001)
Angewandte Chemie - International Edition
, vol.40
, Issue.13
, pp. 2534-2536
-
-
Sakaguchi, S.1
Kubo, T.2
Ishii, Y.3
-
36
-
-
4043050887
-
Iridium-catalyzed coupling of simple primary or secondary amines, aldehydes and trimethylsilylacetylene: Preparation of propargylic amines
-
Sakaguchi, S.; Mizuta, T.; Furuwan, M. i.; Kubo, T.; Ishii, Y. Iridium-catalyzed coupling of simple primary or secondary amines, aldehydes and trimethylsilylacetylene: Preparation of propargylic amines Chem. Commun. 2004, 1638-1639 (Pubitemid 39078887)
-
(2004)
Chemical Communications
, Issue.14
, pp. 1638-1639
-
-
Sakaguchi, S.1
Mizuta, T.2
Furuwan, M.3
Kubo, T.4
Ishii, Y.5
-
37
-
-
0001751065
-
Direct addition of TMS-acetylene to aldimines catalyzed by a simple, commercially available Ir(I) complex
-
DOI 10.1021/ol017022q
-
Carreira, E. M.; Fischer, C. Direct addition of TMS-acetylene to aldimines catalyzed by a simple, commercially available Ir(I) complex Org. Lett. 2001, 3, 4319-4321 (Pubitemid 33627275)
-
(2001)
Organic Letters
, vol.3
, Issue.26
, pp. 4319-4321
-
-
Fischer, C.1
Carreira, E.M.2
-
38
-
-
3042748174
-
2 as an additive in Ir(I)-catalyzed addition of silylacetylenes to imines: Expeditious synthesis of propargylic amines
-
2 as an additive in Ir(I)-catalyzed addition of silylacetylenes to imines: Expeditious synthesis of propargylic amines Synthesis 2004, 1497-1503 (Pubitemid 38887970)
-
(2004)
Synthesis
, Issue.9
, pp. 1497-1503
-
-
Fischer, C.1
Carreira, E.M.2
-
39
-
-
0037157090
-
Enantioselective direct-addition of terminal alkynes to imines catalyzed by copper(I)pybox complex in water and in toluene
-
DOI 10.1021/ja026007t
-
Wei, C.; Li, C.-J. Enantioselective direct addition of alkynes to imines catalyzed by copper(I)pybox complex in water and in toluene J. Am. Chem. Soc. 2002, 124, 5638-5639 (Pubitemid 34533493)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.20
, pp. 5638-5639
-
-
Wei, C.1
Li, C.-J.2
-
40
-
-
1942469512
-
Cu(I)-catalyzed direct addition and asymmetric addition of terminal alkynes to imines
-
DOI 10.1073/pnas.0307150101
-
Wei, C.; Mague, J. T.; Li, C.-J. Cu(I)-catalyzed direct addition and asymmetric addition of terminal alkynes to imines Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 5749-5754 (Pubitemid 38520472)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.16
, pp. 5749-5754
-
-
Wei, C.1
Mague, J.T.2
Li, C.-J.3
-
41
-
-
53849109164
-
Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide
-
Yoo, W.-J.; Li, C.-J. Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide Adv. Syn. Catal. 2008, 350, 1503-1506
-
(2008)
Adv. Syn. Catal.
, vol.350
, pp. 1503-1506
-
-
Yoo, W.-J.1
Li, C.-J.2
-
42
-
-
29844454802
-
A silver-catalyzed domino route toward 1,2-dihydroquinoline derivatives from simple anilines and alkynes
-
DOI 10.1021/ol050826b
-
Luo, Y.; Li, Z.; Li, C.-J. A silver-catalyzed domino route toward 1,2-dihydroquinoline derivatives from simple anilines and alkynes Org. Lett. 2005, 7, 2675-2678 (Pubitemid 43034236)
-
(2005)
Organic Letters
, vol.7
, Issue.13
, pp. 2675-2678
-
-
Luo, Y.1
Li, Z.2
Li, C.-J.3
-
43
-
-
0030765701
-
Mannich reactions of a resin-bound terminal alkyne
-
Youngman, M. A.; Dax, S. L. Mannich reactions of a resin-bound terminal alkyne Tetrahedron Lett. 1997, 38, 6347-6350
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 6347-6350
-
-
Youngman, M.A.1
Dax, S.L.2
-
44
-
-
0035031504
-
A microwave-enhanced, solventless Mannich condensation on CuI-doped alumina
-
Kabalka, G. W.; Wang, L.; Pagni, R. M. A microwave-enhanced, solventless Mannich condensation on CuI-doped alumina Synlett. 2001, 676-678 (Pubitemid 32434200)
-
(2001)
Synlett
, Issue.5
, pp. 676-678
-
-
Kabalka, G.W.1
Wang, L.2
Pagni, R.M.3
-
45
-
-
0042125406
-
A highly efficient three-component coupling of aldehyde, alkyne, and amines via C-H activation catalyzed by gold in water
-
DOI 10.1021/ja0359299
-
Wei, C.; Li, C.-J. A highly efficient three-component coupling of aldehyde, alkyne, and amines via C-H activation catalyzed by gold in water J. Am. Chem. Soc. 2003, 125, 9584-9585 (Pubitemid 36975910)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.32
, pp. 9584-9585
-
-
Wei, C.1
Li, C.-J.2
-
46
-
-
42749087843
-
Gold-catalyzed reactions of C-H bonds
-
Skouta, R.; Li, C.-J. Gold-catalyzed reactions of C-H bonds Tetrahedron 2008, 64, 4917-4938
-
(2008)
Tetrahedron
, vol.64
, pp. 4917-4938
-
-
Skouta, R.1
Li, C.-J.2
-
47
-
-
58649115594
-
Gold(III) complex-catalyzed synthesis of propargylamines via a three-component coupling reaction of aldehydes, amines and alkynes
-
references therein
-
Lo, V. K.-Y.; Kung, K. K.-Y.; Wong, M.-K.; Che, C.-M. Gold(III) complex-catalyzed synthesis of propargylamines via a three-component coupling reaction of aldehydes, amines and alkynes J. Organomet. Chem. 2009, 694, 583-591 and references therein
-
(2009)
J. Organomet. Chem.
, vol.694
, pp. 583-591
-
-
Lo, V.K.-Y.1
Kung, K.K.-Y.2
Wong, M.-K.3
Che, C.-M.4
-
48
-
-
0344496729
-
The first silver-catalyzed three-component reaction of aldehyde, alkyne, and amine
-
Wei, C. M.; Li, Z. G.; Li, C.-J. The first silver-catalyzed three-component reaction of aldehyde, alkyne, and amine Org. Lett. 2003, 5, 4473-4475
-
(2003)
Org. Lett.
, vol.5
, pp. 4473-4475
-
-
Wei, C.M.1
Li, Z.G.2
Li, C.-J.3
-
49
-
-
1242270576
-
Three-component coupling of aldehyde, alkyne, and amine catalyzed by silver in ionic liquid
-
DOI 10.1016/j.tetlet.2004.01.044
-
Li, Z.; Wei, C.; Chen, L.; Varma, R. S.; Li, C.-J. Three component coupling of aldehyde, alkyne and amine catalyzed by silver in ionic liquid Tetrahedron Lett. 2004, 45, 2443-2446 (Pubitemid 38230351)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.11
, pp. 2443-2446
-
-
Li, Z.1
Wei, C.2
Chen, L.3
Varma, R.S.4
Li, C.-J.5
-
50
-
-
37749027774
-
AgY zeolite as catalyst for the effective three-component synthesis of propargylamines
-
Maggi, R.; Bello, A.; Oro, C.; Sartori, G.; Soldi, L. AgY zeolite as catalyst for the effective three-component synthesis of propargylamines Tetrahedron 2008, 64, 1435--1439, and refs cited therein
-
(2008)
Tetrahedron
, vol.64
, pp. 1435-1439
-
-
Maggi, R.1
Bello, A.2
Oro, C.3
Sartori, G.4
Soldi, L.5
-
51
-
-
34548725044
-
Dual catalysis: A combined enantioselective brønsted acid and metal-catalyzed reaction - Metal catalysis with chiral counterions
-
DOI 10.1002/anie.200702439
-
Rueping, M.; Antonchick, A. P.; Brinkmann, C. Dual catalysis: A combined enantioselective Brønsted acid and metal-catalyzed reaction-metal catalysis with chiral counterions Angew. Chem., Int. Ed. 2007, 46, 6903-6906 (Pubitemid 47425815)
-
(2007)
Angewandte Chemie - International Edition
, vol.46
, Issue.36
, pp. 6903-6906
-
-
Rueping, M.1
Antonchick, A.P.2
Brinkmann, C.3
-
52
-
-
0346243940
-
Enantioselective, Copper(I)-Catalyzed Three-Component Reaction for the Preparation of Propargylamines
-
DOI 10.1002/anie.200352578
-
Gommermann, N.; Koradin, C.; Polborn, K.; Knochel, P. Enantioselective, copper(I)-catalyzed three-component reaction for the preparation of propargylamines Angew. Chem., Int. Ed. 2003, 42, 5763-5766 (Pubitemid 37522573)
-
(2003)
Angewandte Chemie - International Edition
, vol.42
, Issue.46
, pp. 5763-5766
-
-
Gommermann, N.1
Koradin, C.2
Polborn, K.3
Knochel, P.4
-
53
-
-
33744823250
-
Practical highly enantioselective synthesis of propargylamines through a copper-catalyzed one-pot three-component condensation reaction
-
DOI 10.1002/chem.200501233
-
Gommermann, N.; Knochel, P. Practical highly enantioselective synthesis of propargylamines through a copper-catalyzed one-pot three-component condensation reaction Chem. - Eur. J. 2006, 12, 4380-4392 and references therein (Pubitemid 43829109)
-
(2006)
Chemistry - A European Journal
, vol.12
, Issue.16
, pp. 4380-4392
-
-
Gommermann, N.1
Knochel, P.2
-
54
-
-
27444434315
-
Preparation of functionalized primary chiral amines and amides via an enantioselective three-component synthesis of propargylamines
-
DOI 10.1016/j.tet.2005.08.064, PII S0040402005014602, Multicomponent Reactions
-
Gommermann, N.; Knochel, P. Preparation of functionalized primary chiral amines and amides via an enantioselective three-component synthesis of propargylamines Tetrahedron 2005, 61, 11418-11426 (Pubitemid 41532310)
-
(2005)
Tetrahedron
, vol.61
, Issue.48
, pp. 11418-11426
-
-
Gommermann, N.1
Knochel, P.2
-
55
-
-
9344245165
-
Readily available biaryl P,N ligands for asymmetric catalysis
-
DOI 10.1002/anie.200461286
-
Knopfel, T. F.; Aschwanden, P.; Ichikawa, T.; Watanabe, T.; Carreira, E. M. Readily available biaryl P, N ligands for asymmetric catalysis Angew. Chem., Int. Ed. 2004, 43, 5971-5973 (Pubitemid 39555511)
-
(2004)
Angewandte Chemie - International Edition
, vol.43
, Issue.44
, pp. 5971-5973
-
-
Knopfel, T.F.1
Aschwanden, P.2
Ichikawa, T.3
Watanabe, T.4
Carreira, E.M.5
-
56
-
-
1642487346
-
Microwave-promoted three-component coupling of aldehyde, alkyne, and amine via C-H activation catalyzed by copper in water
-
DOI 10.1021/ol049936t
-
Shi, L.; Tu, Y.-Q.; Wang, M.; Zhang, F.-M.; Fan, C.-A. Microwave-promoted three-component coupling of aldehyde, alkyne, and amine via C-H activation catalyzed by copper in water Org. Lett. 2004, 6, 1001-1003 (Pubitemid 38402682)
-
(2004)
Organic Letters
, vol.6
, Issue.6
, pp. 1001-1003
-
-
Shi, L.1
Tu, Y.-Q.2
Wang, M.3
Zhang, F.-M.4
Fan, C.-A.5
-
57
-
-
12344319135
-
Microwave-assisted Cu (I) catalyzed solvent-free three component coupling of aldehyde, alkyne and amine
-
DOI 10.1002/qsar.200420034
-
Ju, Y.; Li, C.-J.; Varma, R. S. Microwave-assisted Cu(I) catalyzed solvent-free three component coupling of aldehyde, alkyne and amine QSAR Comb. Sci. 2004, 23, 891-894 (Pubitemid 40127760)
-
(2004)
QSAR and Combinatorial Science
, vol.23
, Issue.10
, pp. 891-894
-
-
Ju, Y.1
Li, C.-J.2
Varma, R.S.3
-
58
-
-
16244411153
-
An efficient synthesis of propargylamines via C-H activation catalyzed by copper(I) in ionic liquids
-
DOI 10.1039/b416268d
-
Park, S. B.; Alper, H. An efficient synthesis of propargylamines via C-H activation catalyzed by copper(I) in ionic liquids Chem. Commun. 2005, 1315-1317 (Pubitemid 40459985)
-
(2005)
Chemical Communications
, Issue.10
, pp. 1315-1317
-
-
Park, S.B.1
Alper, H.2
-
59
-
-
5144230467
-
Mild and efficient synthesis of propargylamines by copper-catalyzed Mannich reaction
-
Bieber, L. W.; da Silva, M. F. Mild and efficient synthesis of propargylamines by copper-catalyzed Mannich reaction Tetrahedron Lett. 2004, 45, 8281-8283
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 8281-8283
-
-
Bieber, L.W.1
Da Silva, M.F.2
-
60
-
-
24344476717
-
Ultrasound-assisted rapid and efficient synthesis of propargylamines
-
DOI 10.1016/j.tetlet.2005.08.047, PII S0040403905017818
-
Sreedhar, B.; Reddy, P. S.; Prakash, B. V.; Ravindra, A. Ultrasound-assisted rapid and efficient synthesis of propargylamines Tetrahedron Lett. 2005, 46, 7019-7022 (Pubitemid 41253838)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.41
, pp. 7019-7022
-
-
Sreedhar, B.1
Surendra Reddy, P.2
Veda Prakash, B.3
Ravindra, A.4
-
61
-
-
33748272697
-
Diastereoselective aldehyde-alkyne-amine coupling of ∝-hydroxylated compounds
-
Huang, B.; Yao, X.; Li, C.-J. Diastereoselective aldehyde-alkyne-amine coupling of ∝-hydroxylated compounds Adv. Catal. Synth. 2006, 348, 1528-1532
-
(2006)
Adv. Catal. Synth.
, vol.348
, pp. 1528-1532
-
-
Huang, B.1
Yao, X.2
Li, C.-J.3
-
62
-
-
58249108032
-
Copper-catalyzed decarboxylative coupling of sp3-hybridized carbons of aI-amino acids
-
Bi, H. P.; Zhao, L.; Liang, Y. M.; Li, C.-J. Copper-catalyzed decarboxylative coupling of sp3-hybridized carbons of aI-amino acids Angew. Chem., Int. Ed. 2009, 48, 792-795
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 792-795
-
-
Bi, H.P.1
Zhao, L.2
Liang, Y.M.3
Li, C.-J.4
-
63
-
-
65249146649
-
Cross-dehydrogenative-coupling (CDC): Explore C-C bond formations beyond functional group transformations
-
Li, C.-J. Cross-dehydrogenative-coupling (CDC): Explore C-C bond formations beyond functional group transformations Acc. Chem. Res. 2009, 42, 335-344
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 335-344
-
-
Li, C.-J.1
-
64
-
-
33645857392
-
Studies on Cu-catalyzed asymmetric alkynylation of tetrahydroisoquinoline derivatives
-
Li, Z.; MacLeod, P. D.; Li, C.-J. Studies on Cu-catalyzed asymmetric alkynylation of tetrahydroisoquinoline derivatives Tetrahedron: Asymmetry 2006, 17, 590-597
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 590-597
-
-
Li, Z.1
MacLeod, P.D.2
Li, C.-J.3
-
65
-
-
12344286967
-
3 C-H bonds adjacent to a nitrogen atom
-
DOI 10.1021/ol047814v
-
Li, Z.; Li, C.-J. Catalytic enantioselective alkynylation of prochiral sp3 C-H bonds adjacent to a nitrogen atom Org. Lett. 2004, 6, 4997-4999 (Pubitemid 40125861)
-
(2004)
Organic Letters
, vol.6
, Issue.26
, pp. 4997-4999
-
-
Li, Z.1
Li, C.-J.2
-
66
-
-
63849187549
-
Synthesis of propargylamines by a copper-catalyzed tandem anti-Markovnikov hydroamination and alkyne addition
-
Zhou, L.; Bohle, D. S.; Jiang, H. F.; Li, C.-J. Synthesis of propargylamines by a copper-catalyzed tandem anti-Markovnikov hydroamination and alkyne addition Synlett 2009, 937-940
-
(2009)
Synlett
, pp. 937-940
-
-
Zhou, L.1
Bohle, D.S.2
Jiang, H.F.3
Li, C.-J.4
-
67
-
-
65249119733
-
Iron-catalyzed three-component coupling of aldehyde, alkyne and amine under neat conditions in air
-
Chen, W. W.; Nguyen, R. V.; Li, C.-J. Iron-catalyzed three-component coupling of aldehyde, alkyne and amine under neat conditions in air Tetrahedron Lett. 2009, 50, 2895-2898
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 2895-2898
-
-
Chen, W.W.1
Nguyen, R.V.2
Li, C.-J.3
-
68
-
-
60749087624
-
Iron-catalyzed ligand-free three-component coupling reactions of aldehydes, terminal alkynes, and amines
-
Li, P.; Zhang, Y.; Wang, L. Iron-catalyzed ligand-free three-component coupling reactions of aldehydes, terminal alkynes, and amines Chem. - Eur. J. 2009, 15, 2045-2049
-
(2009)
Chem. - Eur. J.
, vol.15
, pp. 2045-2049
-
-
Li, P.1
Zhang, Y.2
Wang, L.3
-
69
-
-
0037068159
-
Cu(I)Br mediated coupling of alkynes with N-acylimine and N-acyliminium ions in water
-
DOI 10.1016/S0040-4039(02)01197-8, PII S0040403902011978
-
Zhang, J.; Wei, C.; Li, C.-J. Cu(I)Br-mediated coupling of alkynes with N -acylimine and N -acyliminium ions in water Tetrahedron Lett. 2002, 43, 5731-5734 (Pubitemid 34876365)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.33
, pp. 5731-5733
-
-
Zhang, J.1
Wei, C.2
Li, C.-J.3
-
70
-
-
2342468598
-
Copper-catalyzed coupling of imines, acid chlorides, and alkynes: A multicomponent route to propargylamides
-
Black, A. D.; Arndtsen, B. A. Copper-catalyzed coupling of imines, acid chlorides, and alkynes: a multicomponent route to propargylamides Org. Lett. 2004, 6, 1107-1110
-
(2004)
Org. Lett.
, vol.6
, pp. 1107-1110
-
-
Black, A.D.1
Arndtsen, B.A.2
-
71
-
-
2442564600
-
Zn-alkynylide additions to acyl iminiums
-
DOI 10.1021/ol049578u
-
Fischer, C.; Carreira, E. M. Zn-alkynylide additions to acyl iminiums Org. Lett. 2004, 6, 1497-1499 (Pubitemid 38626338)
-
(2004)
Organic Letters
, vol.6
, Issue.9
, pp. 1497-1499
-
-
Fischer, C.1
Carreira, E.M.2
-
72
-
-
33645893043
-
Gold-catalyzed coupling of alkynes and acyl iminiums
-
Wei, C.; Li, C.-J. Gold-catalyzed coupling of alkynes and acyl iminiums Lett. Org. Chem. 2005, 2, 410-414
-
(2005)
Lett. Org. Chem.
, vol.2
, pp. 410-414
-
-
Wei, C.1
Li, C.-J.2
-
73
-
-
54749113948
-
New approaches to functionalize glycine derivatives via direct C-C bond formation
-
Zhao, L.; Li, C.-J. New approaches to functionalize glycine derivatives via direct C-C bond formation Angew. Chem., Int. Ed. 2008, 47, 7075-7078
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 7075-7078
-
-
Zhao, L.1
Li, C.-J.2
-
74
-
-
63149103163
-
Site-specific C-functionalization of free (NH)-peptides and glycine derivatives via direct C-H bond functionalization
-
Zhao, L.; Basle, O.; Li, C.-J. Site-specific C-functionalization of free (NH)-peptides and glycine derivatives via direct C-H bond functionalization Proc. Natl. Acad. Sci. U.S.A. 2009, 106, 4106-4111
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 4106-4111
-
-
Zhao, L.1
Basle, O.2
Li, C.-J.3
-
75
-
-
33846522323
-
Efficient ruthenium and copper cocatalzyed five-component coupling to form dipropargyl amines under mild conditions in water
-
Bonfield, E. R.; Li, C.-J. Efficient ruthenium and copper cocatalzyed five-component coupling to form dipropargyl amines under mild conditions in water Org. Biomol. Chem. 2007, 5, 435-437
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 435-437
-
-
Bonfield, E.R.1
Li, C.-J.2
-
76
-
-
53849102601
-
3 coupling and [2 + 2+2] cycloaddition reaction
-
3 coupling and [2 + 2+2] cycloaddition reaction Adv. Synth. Catal. 2008, 350, 370-374
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 370-374
-
-
Bonfield, E.R.1
Li, C.-J.2
-
77
-
-
0037613482
-
The first conjugate addition reaction of terminal alkynes catalytic in copper: Conjugate addition of alkynes in water
-
Carreira, E. M.; Knopfel, T. F. The first conjugate addition reaction of terminal alkynes catalytic in copper: Conjugate addition of alkynes in water J. Am. Chem. Soc. 2003, 125, 6054-6055
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 6054-6055
-
-
Carreira, E.M.1
Knopfel, T.F.2
-
78
-
-
22144481646
-
Catalytic, enantioselective, conjugate alkyne addition
-
DOI 10.1021/ja052411r
-
Knopfel, T. F.; Zarotti, P.; Ichikawa, T.; Carreira, E. M. Catalytic, enantioselective, conjugate alkyne addition J. Am. Chem. Soc. 2005, 127, 9682-9683 (Pubitemid 40981522)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.27
, pp. 9682-9683
-
-
Knopfel, T.F.1
Zarotti, P.2
Ichikawa, T.3
Carreira, E.M.4
-
79
-
-
34447295387
-
I-catalyzed conjugate addition of ethyl propiolate
-
DOI 10.1002/anie.200701098
-
Fujimori, S.; M. Carreira, E. M. Cu(I)-catalyzed conjugate addition of ethyl propiolate Angew. Chem., Int. Ed. 2007, 46, 4964-4967 (Pubitemid 47055970)
-
(2007)
Angewandte Chemie - International Edition
, vol.46
, Issue.26
, pp. 4964-4967
-
-
Fujimori, S.1
Carreira, E.M.2
-
80
-
-
1542268871
-
Facile and selective copper-palladium catalyzed addition of terminal alkynes to activated alkynes in water
-
DOI 10.1016/j.tetlet.2004.02.038, PII S0040403904003375
-
Chen, L.; Li, C.-J. Facile and selective copper-palladium catalyzed addition of terminal alkynes to activated alkynes in water Tetrahedron Lett. 2004, 45, 2771-2774 (Pubitemid 38317144)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.13
, pp. 2771-2774
-
-
Chen, L.1
Li, C.-J.2
-
81
-
-
9144270060
-
The first palladium-catalyzed 1,4-addition of terminal alkynes to conjugated enones
-
DOI 10.1039/b407936a
-
Chen, L.; Li, C.-J. The first palladium-catalyzed 1,4-addition of terminal alkynes to conjugated enones Chem. Commun. 2004, 2362-2364 (Pubitemid 39545930)
-
(2004)
Chemical Communications
, Issue.20
, pp. 2362-2364
-
-
Chen, L.1
Li, C.-J.2
-
82
-
-
4143079275
-
Rhodium-catalyzed 1,4-addition of terminal alkynes to vinyl ketones
-
DOI 10.1016/j.tetlet.2004.07.036, PII S0040403904015102
-
Lerum, R. V.; Chisholm, J. D. Rhodium-catalyzed 1,4-addition of terminal alkynes to vinyl ketones Tetrahedron Lett. 2004, 45, 6591-6594 (Pubitemid 39091862)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.35
, pp. 6591-6594
-
-
Lerum, R.V.1
Chisholm, J.D.2
-
83
-
-
49149117052
-
Palladium-catalyzed 1,4-addition of terminal alkynes to unsaturated carbonyl compounds promoted by electron-rich ligands
-
Zhou, L.; Chen, L.; Skouta, R.; Li, C.-J. Palladium-catalyzed 1,4-addition of terminal alkynes to unsaturated carbonyl compounds promoted by electron-rich ligands Org. Biomol. Chem. 2008, 6, 2969-2977
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 2969-2977
-
-
Zhou, L.1
Chen, L.2
Skouta, R.3
Li, C.-J.4
-
84
-
-
70350518094
-
Cu-catalyzed amine-alkyne-alkyne addition reaction: An efficient method for the synthesis of γ,δ-alkynyl-β-amino acid derivatives
-
Zhou, L.; Suai, Q.; Jiang, H.-F.; Li, C.-J. Cu-catalyzed amine-alkyne-alkyne addition reaction: an efficient method for the synthesis of γ,δ-alkynyl-β-amino acid derivatives Chem. - Eur. J. 2009, 15, 11668-11674
-
(2009)
Chem. - Eur. J.
, vol.15
, pp. 11668-11674
-
-
Zhou, L.1
Suai, Q.2
Jiang, H.-F.3
Li, C.-J.4
|