-
1
-
-
4143051292
-
Nucleophilic carbenes in asymmetric organocatalysis
-
Enders, D. & Balensiefer, T. Nucleophilic carbenes in asymmetric organocatalysis. Acc. Chem. Res. 37, 534-541 (2004).
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 534-541
-
-
Enders, D.1
Balensiefer, T.2
-
2
-
-
38349109278
-
Organocatalysis by N-heterocyclic carbenes
-
Enders, D., Niemeier, O. & Henseler, A. Organocatalysis by N-heterocyclic carbenes. Chem. Rev. 107, 5606-5655 (2007).
-
(2007)
Chem. Rev.
, vol.107
, pp. 5606-5655
-
-
Enders, D.1
Niemeier, O.2
Henseler, A.3
-
3
-
-
34250870731
-
N-Heterocyclic carbenes as organocatalysts
-
Marion, N., Dez-Gonzlez, S. & Nolan, S. P. N-Heterocyclic carbenes as organocatalysts. Angew. Chem. Int. Ed. 46, 2988-3000 (2007).
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 2988-3000
-
-
Marion, N.1
Dez-Gonzlez, S.2
Nolan, S.P.3
-
4
-
-
82455205867
-
Cooperative Lewis acid/N-heterocyclic carbene catalysis
-
Cohen, D. T. & Scheidt, K. A. Cooperative Lewis acid/N-heterocyclic carbene catalysis. Chem. Sci. 3, 53-57 (2012).
-
(2012)
Chem. Sci.
, vol.3
, pp. 53-57
-
-
Cohen, D.T.1
Scheidt, K.A.2
-
5
-
-
84869460648
-
A continuum of progress: Applications of N-hetereocyclic carbene catalysis in total synthesis
-
Izquierdo, J., Hutson, G. E., Cohen, D. T. & Scheidt, K. A. A continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis. Angew. Chem. Int. Ed. 51, 11686-11698 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 11686-11698
-
-
Izquierdo, J.1
Hutson, G.E.2
Cohen, D.T.3
Scheidt, K.A.4
-
6
-
-
84862577173
-
Exploiting acyl and enol azolium intermediates via N-heterocyclic carbene-catalyzed reactions of α-reducible aldehydes
-
Vora, H. U., Wheeler, P. & Rovis, T. Exploiting acyl and enol azolium intermediates via N-heterocyclic carbene-catalyzed reactions of α-reducible aldehydes. Adv. Synth. Catal. 354, 1617-1639 (2012).
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 1617-1639
-
-
Vora, H.U.1
Wheeler, P.2
Rovis, T.3
-
7
-
-
84859747983
-
Organocatalytic umpolung: N-heterocyclic carbenes and beyond
-
Bugaut, X. & Glorius, F. Organocatalytic umpolung: N-heterocyclic carbenes and beyond. Chem. Soc. Rev. 41, 3511-3522 (2012).
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 3511-3522
-
-
Bugaut, X.1
Glorius, F.2
-
8
-
-
84875799416
-
Acyl anion free N-heterocyclic carbene organocatalysis
-
Ryan, S. J., Candish, L. & Lupton, D. W. Acyl anion free N-heterocyclic carbene organocatalysis. Chem. Soc. Rev. 42, 4906-4917 (2013).
-
(2013)
Chem. Soc. Rev.
, vol.42
, pp. 4906-4917
-
-
Ryan, S.J.1
Candish, L.2
Lupton, D.W.3
-
9
-
-
84903539227
-
An overview of N-heterocyclic carbenes
-
Hopkinson, M. N., Richter, C., Schedler, M. & Glorius, F. An overview of N-heterocyclic carbenes. Nature 510, 485-496 (2014).
-
(2014)
Nature
, vol.510
, pp. 485-496
-
-
Hopkinson, M.N.1
Richter, C.2
Schedler, M.3
Glorius, F.4
-
10
-
-
79958213157
-
Asymmetric N-heterocyclic carbene (NHC) catalyzed acyl anion reactivity
-
Vora, H. U. & Rovis, T. Asymmetric N-heterocyclic carbene (NHC) catalyzed acyl anion reactivity. Aldrichim. Acta 44, 3-11 (2011).
-
(2011)
Aldrichim. Acta
, vol.44
, pp. 3-11
-
-
Vora, H.U.1
Rovis, T.2
-
11
-
-
79960063988
-
Catalytic asymmetric intermolecular Stetter reaction of enals with nitroalkenes: Enhancement of catalytic efficiency through bifunctional additives
-
DiRocco, D. A. & Rovis, T. Catalytic asymmetric intermolecular Stetter reaction of enals with nitroalkenes: enhancement of catalytic efficiency through bifunctional additives. J. Am. Chem. Soc. 133, 10402-10405 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 10402-10405
-
-
DiRocco, D.A.1
Rovis, T.2
-
12
-
-
82455205692
-
Enantioselective Stetter reactions of enals and modified chalcones catalyzed by N-heterocyclic carbenes
-
Fang, X. Q., Chen, X. K., Lv, H. & Chi, Y. R. Enantioselective Stetter reactions of enals and modified chalcones catalyzed by N-heterocyclic carbenes. Angew. Chem. Int. Ed. 50, 11782-11785 (2011).
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 11782-11785
-
-
Fang, X.Q.1
Chen, X.K.2
Lv, H.3
Chi, Y.R.4
-
13
-
-
84878071101
-
Enantioselective N-heterocyclic carbene catalyzed aza-benzoin reaction of enals with activated ketimines
-
Sun, L.-H., Liang, Z.-Q., Jia, W.-Q. & Ye, S. Enantioselective N-heterocyclic carbene catalyzed aza-benzoin reaction of enals with activated ketimines. Angew. Chem. Int. Ed. 52, 5803-5806 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 5803-5806
-
-
Sun, L.-H.1
Liang, Z.-Q.2
Jia, W.-Q.3
Ye, S.4
-
14
-
-
84903139527
-
N-Heterocyclic carbenecatalyzed chemoselective cross-aza-benzoin reaction of enals with isatin-derived ketimines: Access to chiral quaternary aminooxindoles
-
Xu, J., Mou, C., Zhu, T., Song, B.-A. & Chi, Y. R. N-Heterocyclic carbenecatalyzed chemoselective cross-aza-benzoin reaction of enals with isatin-derived ketimines: access to chiral quaternary aminooxindoles. Org. Lett. 16, 3272-3275 (2014).
-
(2014)
Org. Lett.
, vol.16
, pp. 3272-3275
-
-
Xu, J.1
Mou, C.2
Zhu, T.3
Song, B.-A.4
Chi, Y.R.5
-
15
-
-
10044249952
-
Organocatalyzed conjugate umpolung of α,β- unsaturated aldehydes for the synthesis of γ-butyrolactones
-
Burstein, C. & Glorius, F. Organocatalyzed conjugate umpolung of α,β- unsaturated aldehydes for the synthesis of γ-butyrolactones. Angew. Chem. Int. Ed. 43, 6205-6208 (2004).
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 6205-6208
-
-
Burstein, C.1
Glorius, F.2
-
16
-
-
7744232978
-
N-Heterocyclic carbene-catalyzed generation of homoenolates: γ-butyrolactones by direct annulations of enals and aldehydes
-
Sohn, S. S., Rosen, E. L. & Bode, J. W. N-Heterocyclic carbene-catalyzed generation of homoenolates: γ-butyrolactones by direct annulations of enals and aldehydes. J. Am. Chem. Soc. 126, 14370-14371 (2004).
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 14370-14371
-
-
Sohn, S.S.1
Rosen, E.L.2
Bode, J.W.3
-
17
-
-
34247874549
-
Highly stereoselective formal [3+3] cycloaddition of enals and azomethine imines catalyzed by N-heterocyclic carbenes
-
Chan, A. & Scheidt, K. A. Highly stereoselective formal [3+3] cycloaddition of enals and azomethine imines catalyzed by N-heterocyclic carbenes. J. Am. Chem. Soc. 129, 5334-5335 (2007).
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 5334-5335
-
-
Chan, A.1
Scheidt, K.A.2
-
18
-
-
39749122608
-
Highly diastereo- and enantioselective additions of homoenolates to nitrones catalyzed by N-heterocyclic carbenes
-
Phillips, E. M., Reynolds, T. E. & Scheidt, K. A. Highly diastereo- and enantioselective additions of homoenolates to nitrones catalyzed by N-heterocyclic carbenes. J. Am. Chem. Soc. 130, 2416-2417 (2008).
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 2416-2417
-
-
Phillips, E.M.1
Reynolds, T.E.2
Scheidt, K.A.3
-
19
-
-
67749124296
-
Cyclic ketimines as superior electrophiles for NHC-catalyzed homoenolate additions with broad scope and low catalyst loadings
-
Rommel, M., Fukuzumi, T. & Bode, J. W. Cyclic ketimines as superior electrophiles for NHC-catalyzed homoenolate additions with broad scope and low catalyst loadings. J. Am. Chem. Soc. 130, 17266-17267 (2008).
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 17266-17267
-
-
Rommel, M.1
Fukuzumi, T.2
Bode, J.W.3
-
20
-
-
77956041225
-
Cooperative catalysis by carbenes and Lewis acids in a highly stereoselective route to γ-lactams
-
Raup, D. E. A., Cardinal-David, B., Holte, D. & Scheidt, K. A. Cooperative catalysis by carbenes and Lewis acids in a highly stereoselective route to γ-lactams. Nature Chem. 2, 766-771 (2010).
-
(2010)
Nature Chem.
, vol.2
, pp. 766-771
-
-
Raup, D.E.A.1
Cardinal-David, B.2
Holte, D.3
Scheidt, K.A.4
-
21
-
-
80051589227
-
N-Heterocyclic carbene and Bronsted acid cooperative catalysis: Asymmetric synthesis of trans-γ-lactams
-
Zhao, X., DiRocco, D. A. & Rovis, T. N-Heterocyclic carbene and Bronsted acid cooperative catalysis: asymmetric synthesis of trans-γ-lactams. J. Am. Chem. Soc. 133, 12466-12469 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 12466-12469
-
-
Zhao, X.1
DiRocco, D.A.2
Rovis, T.3
-
22
-
-
84884832672
-
β -Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysis.
-
Fu, Z., Xu, J., Zhu, T., Leong, W. W. Y. & Chi, Y. R. β-Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysis. Nature Chem. 5, 835-839 (2013).
-
(2013)
Nature Chem.
, vol.5
, pp. 835-839
-
-
Fu, Z.1
Xu, J.2
Zhu, T.3
Leong, W.W.Y.4
Chi, Y.R.5
-
23
-
-
84880764620
-
A dual Lewis base activation strategy for enantioselective carbene-catalyzed annulations
-
Izquierdo, J., Orue, A. & Scheidt, K. A. A dual Lewis base activation strategy for enantioselective carbene-catalyzed annulations. J. Am. Chem. Soc. 135, 10634-10637 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 10634-10637
-
-
Izquierdo, J.1
Orue, A.2
Scheidt, K.A.3
-
24
-
-
84880835415
-
N-Heterocyclic carbene catalyzed [4+3] annulation of enals and o-quinone methides: Highly enantioselective synthesis of benzo-E-lactones
-
Lv, H., Jia, W.-Q., Sun, L.-H. & Ye, S. N-Heterocyclic carbene catalyzed [4+3] annulation of enals and o-quinone methides: highly enantioselective synthesis of benzo-E-lactones. Angew. Chem. Int. Ed. 52, 8607-8610 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 8607-8610
-
-
Lv, H.1
Jia, W.-Q.2
Sun, L.-H.3
Ye, S.4
-
25
-
-
28444444128
-
Enantioselective protonation of catalytically generated chiral enolates as an approach to the synthesis of α-chloroesters
-
Reynolds, N. T. & Rovis, T. Enantioselective protonation of catalytically generated chiral enolates as an approach to the synthesis of α-chloroesters. J. Am. Chem. Soc. 127, 16406-16407 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 16406-16407
-
-
Reynolds, N.T.1
Rovis, T.2
-
26
-
-
33745685959
-
Highly enantioselective azadiene Diels-Alder reactions catalyzed by chiral N-heterocyclic carbenes
-
He, M., Struble, J. R. & Bode, J.W. Highly enantioselective azadiene Diels-Alder reactions catalyzed by chiral N-heterocyclic carbenes. J. Am. Chem. Soc. 128, 8418-8420 (2006).
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 8418-8420
-
-
He, M.1
Struble, J.R.2
Bode, J.W.3
-
27
-
-
78650574221
-
Chiral N-heterocyclic carbenecatalyzed generation of ester enolate equivalents from α,β-unsaturated aldehydes for enantioselective Diels-Alder reactions
-
Kaeobamrung, J., Kozlowski, M. C. & Bode, J.W. Chiral N-heterocyclic carbenecatalyzed generation of ester enolate equivalents from α,β-unsaturated aldehydes for enantioselective Diels-Alder reactions. Proc. Natl Acad. Sci. USA 107, 20661-20665 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 20661-20665
-
-
Kaeobamrung, J.1
Kozlowski, M.C.2
Bode, J.W.3
-
28
-
-
79951805478
-
A highly regio- and stereoselective cascade annulation of enals and benzodi(enone)s catalyzed by N-heterocyclic carbenes
-
Fang, X. Q., Jiang, K., Xing, C., Hao, L. & Chi, Y. R. A highly regio- and stereoselective cascade annulation of enals and benzodi(enone)s catalyzed by N-heterocyclic carbenes. Angew. Chem. Int. Ed. 50, 1910-1913 (2011).
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 1910-1913
-
-
Fang, X.Q.1
Jiang, K.2
Xing, C.3
Hao, L.4
Chi, Y.R.5
-
29
-
-
84890490534
-
Enantioselective N-heterocyclic carbene catalyzed annulation reaction with imidazolidinones
-
McCusker, E. O. & Scheidt, K. A. Enantioselective N-heterocyclic carbene catalyzed annulation reaction with imidazolidinones. Angew. Chem. Int. Ed. 52, 13616-13620 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 13616-13620
-
-
McCusker, E.O.1
Scheidt, K.A.2
-
30
-
-
84870954097
-
Controlled β-protonation and [4+2] cycloaddition of enals and chalcones via N-heterocyclic carbene/acid catalysis: Toward substrate independent reaction control
-
Fu, Z. et al. Controlled β-protonation and [4+2] cycloaddition of enals and chalcones via N-heterocyclic carbene/acid catalysis: toward substrate independent reaction control. Chem. Commun. 49, 261-263 (2013).
-
(2013)
Chem. Commun.
, vol.49
, pp. 261-263
-
-
Fu, Z.1
-
31
-
-
0031055494
-
Total synthesis of (+)-duocarmycin A, epi-(+)-duocarmycin A and their unnatural enantiomers: Assessment of chemical and biological properties
-
Boger, D. L., McKie, J. A., Nishi, T. & Ogiku, T. Total synthesis of (+)-duocarmycin A, epi-(+)-duocarmycin A and their unnatural enantiomers: assessment of chemical and biological properties. J. Am. Chem. Soc. 119, 311-325 (1997).
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 311-325
-
-
Boger, D.L.1
McKie, J.A.2
Nishi, T.3
Ogiku, T.4
-
32
-
-
0028265116
-
Lewis acidpromoted selective rearrangement of trisubstituted epoxides to aldehydes or ketones
-
Maruoka, K., Murase, N., Bureau, R., Ooi, T. & Yamamoto, H. Lewis acidpromoted selective rearrangement of trisubstituted epoxides to aldehydes or ketones. Tetrahedron 50, 3663-3672 (1994).
-
(1994)
Tetrahedron
, vol.50
, pp. 3663-3672
-
-
Maruoka, K.1
Murase, N.2
Bureau, R.3
Ooi, T.4
Yamamoto, H.5
-
33
-
-
33746630913
-
Enantioselective synthesis of vinylcyclopropanes and vinylepoxides mediated by camphor-derived sulfur ylides: Rationale of enantioselectivity, scope, and limitation
-
Deng, X.-M. et al. Enantioselective synthesis of vinylcyclopropanes and vinylepoxides mediated by camphor-derived sulfur ylides: rationale of enantioselectivity, scope, and limitation. J. Am. Chem. Soc. 128, 9730-9740 (2006).
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 9730-9740
-
-
Deng, X.-M.1
-
34
-
-
42949110730
-
Tandem Michael addition/ylide epoxidation for the synthesis of highly functionalized cyclohexadiene epoxide derivatives
-
Wang, Q.-G. et al. Tandem Michael addition/ylide epoxidation for the synthesis of highly functionalized cyclohexadiene epoxide derivatives. J. Am. Chem. Soc. 130, 5408-5409 (2008).
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 5408-5409
-
-
Wang, Q.-G.1
-
35
-
-
0034678033
-
Target-oriented and diversity-oriented organic synthesis in drug discovery
-
Schreiber, S. L. Target-oriented and diversity-oriented organic synthesis in drug discovery. Science 287, 1964-1969 (2000).
-
(2000)
Science
, vol.287
, pp. 1964-1969
-
-
Schreiber, S.L.1
-
36
-
-
33644839988
-
Diversity-oriented syn thesis: Exploring the intersections between chemistry and biology
-
Tan, D. S. Diversity-oriented synthesis: exploring the intersections between chemistry and biology. Nature Chem. Biol. 1, 74-84 (2005).
-
(2005)
Nature Chem. Biol.
, vol.1
, pp. 74-84
-
-
Tan, D.S.1
-
37
-
-
84878933614
-
Asymmetric N-heterocyclic carbene catalyzed addition of enals to nitroalkenes: Controlling stereochemistry via the homoenolate reactivity pathway to access δ-lactams
-
White, N. A., DiRocco, D. A. & Rovis, T. Asymmetric N-heterocyclic carbene catalyzed addition of enals to nitroalkenes: controlling stereochemistry via the homoenolate reactivity pathway to access δ-lactams. J. Am. Chem. Soc. 135, 8504-8507 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 8504-8507
-
-
White, N.A.1
DiRocco, D.A.2
Rovis, T.3
-
38
-
-
84919335951
-
N-Heterocyclic carbene catalyzed switchable reactions of enals with azoalkenes: Formal [4+3] and [4+1] annulations for the synthesis of 1,2-diazepines and pyrazoles
-
Guo, C., Sahoo, B., Daniliuc, C. G. & Glorius, F. N-Heterocyclic carbene catalyzed switchable reactions of enals with azoalkenes: formal [4+3] and [4+1] annulations for the synthesis of 1,2-diazepines and pyrazoles. J. Am. Chem. Soc. 136, 17402-17405 (2014).
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 17402-17405
-
-
Guo, C.1
Sahoo, B.2
Daniliuc, C.G.3
Glorius, F.4
-
39
-
-
38849102334
-
Indolizidine and quinolizidine alkaloids
-
Michael, J. P. Indolizidine and quinolizidine alkaloids. Nat. Prod. Rep. 25, 139-165 (2008).
-
(2008)
Nat. Prod. Rep.
, vol.25
, pp. 139-165
-
-
Michael, J.P.1
-
40
-
-
27644564423
-
Alkaloids from Portulaca oleracea L
-
Xiang, L. et al. Alkaloids from Portulaca oleracea L. Phytochemistry 66, 2595-2601 (2005).
-
(2005)
Phytochemistry
, vol.66
, pp. 2595-2601
-
-
Xiang, L.1
-
41
-
-
0017601102
-
Gephyrotoxins histrionicotoxins and pumiliotoxins from the neotropical frog Dendrobates histrionicus
-
Daly, J. W., Witkop, B., Tokuyama, T., Nishikawa, T. & Karle, I. L. Gephyrotoxins, histrionicotoxins and pumiliotoxins from the neotropical frog Dendrobates histrionicus. Helv. Chim. Acta 60, 1128-1140 (1977).
-
(1977)
Helv. Chim. Acta
, vol.60
, pp. 1128-1140
-
-
Daly, J.W.1
Witkop, B.2
Tokuyama, T.3
Nishikawa, T.4
Karle, I.L.5
-
42
-
-
84872837213
-
Highly enantioselective [3+3] cycloaddition of aromatic azomethine imines with cyclopropanes directed by π-π Stacking interactions
-
Zhou, Y. et al. Highly enantioselective [3+3] cycloaddition of aromatic azomethine imines with cyclopropanes directed by π-π stacking interactions. Angew. Chem. Int. Ed. 52, 1452-1456 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 1452-1456
-
-
Zhou, Y.1
-
43
-
-
84887882521
-
Highly enantioselective dearomatizing formal [3+3] cycloaddition reactions of N-acyliminopyridinium ylides with electrophilic enol carbene intermediates
-
Xu, X., Zavalij, P. Y. & Doyle, M. P. Highly enantioselective dearomatizing formal [3+3] cycloaddition reactions of N-acyliminopyridinium ylides with electrophilic enol carbene intermediates. Angew. Chem. Int. Ed. 52, 12664-12668 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 12664-12668
-
-
Xu, X.1
Zavalij, P.Y.2
Doyle, M.P.3
-
44
-
-
52149113820
-
The advent and development of organocatalysis
-
MacMillan D. W. C. , The advent and development of organocatalysis. Nature 455:304-308 (2008).
-
(2008)
Nature
, vol.455
, pp. 304-308
-
-
MacMillan, D.W.C.1
-
45
-
-
77649087999
-
Organocatalytic cascade reactions as a new tool in total synthesis
-
Grondal, C., Jeanty, M. & Enders, D. Organocatalytic cascade reactions as a new tool in total synthesis. Nature Chem. 2, 167-178 (2010).
-
(2010)
Nature Chem.
, vol.2
, pp. 167-178
-
-
Grondal, C.1
Jeanty, M.2
Enders, D.3
-
46
-
-
0042839400
-
Highly Efficient Synthesis of O-( 2,4-dinitrophenyl) Hydroxylamine. Application to the Synthesis of Substituted N-benzoyliminopyridinium Ylides
-
Legault, C. & Charette, A. B. Highly efficient synthesis of o-(2,4-dinitrophenyl) hydroxylamine. Application to the synthesis of substituted N-benzoyliminopyridinium ylides. J. Org. Chem. 68, 7119-7122 (2003).
-
(2003)
J. Org. Chem.
, vol.68
, pp. 7119-7122
-
-
Legault, C.1
Charette, A.B.2
-
47
-
-
77955838661
-
Silver triflate and N-heterocyclic carbene co-catalyzed reaction of N-(2-alkynylbenzylidene)hydrazine, methanol with α,β-unsaturated aldehyde
-
Chen, Z., Yu, X. & Wu, J. Silver triflate and N-heterocyclic carbene co-catalyzed reaction of N-(2-alkynylbenzylidene)hydrazine, methanol with α,β-unsaturated aldehyde. Chem. Commun. 46, 6356-6358 (2010).
-
(2010)
Chem. Commun.
, vol.46
, pp. 6356-6358
-
-
Chen, Z.1
Yu, X.2
Wu, J.3
-
48
-
-
84890447442
-
Asymmetric synthesis of pyrroloindolones by N-heterocyclic carbene catalyzed [2+3] annulation of α-chloroaldehydes with nitrovinylindoles
-
Ni, Q. et al. Asymmetric synthesis of pyrroloindolones by N-heterocyclic carbene catalyzed [2+3] annulation of α-chloroaldehydes with nitrovinylindoles. Angew. Chem. Int. Ed. 52, 13562-12566 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 13562-12566
-
-
Ni, Q.1
-
49
-
-
3142640259
-
On the mechanism of thiamine action. IV. Evidence from studies on model systems
-
Breslow, R. On the mechanism of thiamine action. IV. Evidence from studies on model systems. J. Am. Chem. Soc. 80, 3719-3726 (1958).
-
(1958)
J. Am. Chem. Soc.
, vol.80
, pp. 3719-3726
-
-
Breslow, R.1
-
50
-
-
84870533278
-
Umpolung by N-heterocyclic carbenes: Generation and reactivity of the elusive 2,2-diamino enols (Breslow intermediates)
-
Berkessel, A. et al. Umpolung by N-heterocyclic carbenes: generation and reactivity of the elusive 2,2-diamino enols (Breslow intermediates). Angew. Chem. Int. Ed. 51, 12370-12374 (2012).
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 12370-12374
-
-
Berkessel, A.1
|