SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Volumn 2013, Issue 4, 2013, Pages 88-97

N-heterocyclic carbene-catalyzed domino hydroacylation/stetter reactions of salicyl alkynylphosphonates and aromatic aldehydes

(3) Wang, Zhen Qiang a Wang, Ying a Shi, De Qing a

a CENTRAL CHINA NORMAL UNIVERSITY (China)

Author keywords

1,4 dicarbonyl compound; Domino reaction; Hydroacylation; N heterocyclic carbene; Phosphonate; Stetter reaction

Indexed keywords

EID: 84882385568 PISSN: 1551-7012 EISSN: 15517004 Source Type: Journal
DOI: 10.3998/ark.5550190.p008.158 Document Type: Article

Times cited : (2)

References (38)

1
- 84890766709
- Wiley-VCH: Weinheim
- For general review on domino reactions, see: (a) Tietze, L. F.; Brasche, G.; Gericke, K. Domino Reactions in Organic Synthesis; Wiley-VCH: Weinheim, 2006. http://dx.doi.org/10.1002/9783527609925
- (2006) Domino Reactions in Organic Synthesis
- Tietze, L.F.¹ Brasche, G.² Gericke, K.³

2
- 7044235263
- (b) Tietze, L. F. Chem. Rev. 1996, 96, 115. http://dx.doi.org/10.1021/ cr950027e PMid:11848746
- (1996) Chem. Rev. , vol.96 , pp. 115
- Tietze, L.F.¹

3
- 30444443444
- (c) Guo, H.-C.; Ma, J.-A. Angew. Chem., Int. Ed. 2006, 45, 354. http://dx.doi.org/10.1002/anie.200500195 PMid:16287187
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 354
- Guo, H.-C.¹ Ma, J.-A.²

4
- 33947198541
- (d) Enders, D.; Grondal, C.; Hüttl, M. R. M. Angew. Chem., Int. Ed. 2007, 46, 1570. http://dx.doi.org/10.1002/anie.200603129 PMid:17225236
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 1570
- Enders, D.¹ Grondal, C.² Hüttl, M.R.M.³

5
- 33750173220
- (e) Tietze, L. F.; Beifuss, U. Angew. Chem., Int. Ed. 1993, 32, 131. http://dx.doi.org/10.1002/anie.199301313
- (1993) Angew. Chem., Int. Ed. , vol.32 , pp. 131
- Tietze, L.F.¹ Beifuss, U.²

6
- 84986448147
- (a) Stetter, H.; Kuhlmann, H. Synthesis 1975, 379 http://dx.doi.org/10. 1055/s-1975-23759.
- (1975) Synthesis , pp. 379
- Stetter, H.¹ Kuhlmann, H.²

7
- 84982075432
- (b) Stetter, H.; Mohrmann, K.-H.; Schlenker, W. Chem. Ber. 1981, 114, 581. - http://dx.doi.org/10.1002/cber.19811140218
- (1981) Chem. Ber. , vol.114 , pp. 581
- Stetter, H.¹ Mohrmann, K.-H.² Schlenker, W.³

8
- 84986527774
- El-Haji, T.; Martin, J. C.; Descotes, G. J. J. Heterocycl. Chem. 1983, 20, 233. http://dx.doi.org/10.1002/jhet.5570200148
- (1983) J. Heterocycl. Chem. , vol.20 , pp. 233
- El-Haji, T.¹ Martin, J.C.² Descotes, G.J.³

9
- 0009562406
- Perrine, D. M.; Kagan, J.; Huang, D. B.; Zeng, K.; Theo, B. K. J. Org. Chem. 1987, 52, 2213. http://dx.doi.org/10.1021/jo00387a019
- (1987) J. Org. Chem. , vol.52 , pp. 2213
- Perrine, D.M.¹ Kagan, J.² Huang, D.B.³ Zeng, K.⁴ Theo, B.K.⁵

10
- 84898740784
- Wynberg, H.; Metselaar, J. Synth. Commun. 1984, 14, 1. http://dx.doi.org/10.1080/00397918408060857
- (1984) Synth. Commun. , vol.14 , pp. 1
- Wynberg, H.¹ Metselaar, J.²

11
- 0001733280
- Jones, T. H.; Franko, J. B.; Blum, M. S.; Fales, H. M. Tetrahedron Lett. 1980, 21, 789. http://dx.doi.org/10.1016/S0040-4039 (00) 71506-1
- (1980) Tetrahedron Lett. , vol.21 , pp. 789
- Jones, T.H.¹ Franko, J.B.² Blum, M.S.³ Fales, H.M.⁴

12
- 4143051292
- NHC
- For recent reviews on NHC catalysis, see: (a) Enders, D.; Balensiefer, T. Acc. Chem. Res. 2004, 37, 534-541; http://dx.doi.org/10.1021/ar030050j PMid:15311952.
- (2004) Acc. Chem. Res. , vol.37 , pp. 534-541
- Enders, D.¹ Balensiefer, T.²

13
- 38349109278
- (b) Enders, D.; Niemeier, O.; Henseler, A. Chem. Rev. 2007, 107, 5606-5655; http://dx.doi.org/10.1021/cr068372z PMid:17956132.
- (2007) Chem. Rev. , vol.107 , pp. 5606-5655
- Enders, D.¹ Niemeier, O.² Henseler, A.³

14
- 34250870731
- (c) Marion, N.; Diéz-González, S.; Nolan, S. P. Angew. Chem. Int. Ed. 2007, 46, 2988-3000; http://dx.doi.org/10.1002/anie.200603380. PMid:17348057.
- (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 2988-3000
- Marion, N.¹ Diéz-González, S.² Nolan, S.P.³

15
- 81255211331
- (d) Biju, A. T.; Kuhl, N.; Glorius, F. Acc. Chem. Res. 2011, 44, 1182-1195; http://dx.doi.org/10.1021/ar2000716. PMid:21751790.
- (2011) Acc. Chem. Res. , vol.44 , pp. 1182-1195
- Biju, A.T.¹ Kuhl, N.² Glorius, F.³

16
- 80052008516
- (e) Shen, L. T.; Shao, P. L.; Ye, S. Adv. Syn. & Catal. 2011, 353, 1943-1948; http://dx.doi.org/10.1002/adsc.201100178
- (2011) Adv. Syn. & Catal. , vol.353 , pp. 1943-1948
- Shen, L.T.¹ Shao, P.L.² Ye, S.³

17
- 79957750879
- (f) Bugaut, X.; Liu, F.; Glorius, F. J. Am. Chem. Soc. 2011, 133, 8130-8133; http://dx.doi.org/10.1021/ja202594g PMid:21520959.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 8130-8133
- Bugaut, X.¹ Liu, F.² Glorius, F.³

18
- 79961153228
- (g) Enders, D.; Grossmann, A.; Huang, H.; Raabe, G. Eur. J. Org. Chem. 2011, 4298-4301; http://dx.doi.org/10.1002/eioc.201100690
- (2011) Eur. J. Org. Chem. , pp. 4298-4301
- Enders, D.¹ Grossmann, A.² Huang, H.³ Raabe, G.⁴

19
- 79955607386
- (h) Park, J. H.; Bhilare, S. V.; Youn, S. W. Org. Lett. 2011, 13, 2228-2231. http://dx.doi.org/10.1021/ol200481u PMid:21446687
- (2011) Org. Lett. , vol.13 , pp. 2228-2231
- Park, J.H.¹ Bhilare, S.V.² Youn, S.W.³

20
- 84855432965
- (i) Grossmann, A.; Enders, D. Angew. Chem. Int. Ed. 2012, 51, 314-325. http://dx.doi.org/10.1002/anie.201105415 PMid:22121084
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 314-325
- Grossmann, A.¹ Enders, D.²

21
- 77951673787
- Biju, A. T.; Wurz, N. E.; Glorius, F. J. Am. Chem. Soc., 2010, 132, 5970-5971. http://dx.doi.org/10.1021/ja102130s PMid:20384303
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 5970-5971
- Biju, A.T.¹ Wurz, N.E.² Glorius, F.³

22
- 79951838576
- (a) Vedachalam, S.; Wong, Q.-L.; Maji, B.; Zeng, J.; Ma, J.; Liu, X.-W. Adv. Synth. Catal. 2011, 353, 219-225; http://dx.doi.org/10.1002/adsc.201000828.
- (2011) Adv. Synth. Catal. , vol.353 , pp. 219-225
- Vedachalam, S.¹ Wong, Q.-L.² Maji, B.³ Zeng, J.⁴ Ma, J.⁵ Liu, X.-W.⁶

23
- 84860335567
- (b) Wang, Z. Q.; Yu, Z. H.; Wang, Y.; Shi, D. Q. Synthesis, 2012, 44, 1559-1568. http://dx.doi.org/10.1055/s-0031-1290976
- (2012) Synthesis , vol.44 , pp. 1559-1568
- Wang, Z.Q.¹ Yu, Z.H.² Wang, Y.³ Shi, D.Q.⁴

24
- 0003858185
- Marcel Dekker: New York
- (a) Engel, R., Ed. Handbook of Organophosphorus Chemistry; Marcel Dekker: New York, 1992;
- (1992) Handbook of Organophosphorus Chemistry
- Engel, R.¹

25
- 0004195923
- John Wiley & Sons: New York
- (b) Hartley, F. R., Ed. The Chemistry of Organophosphorus Compounds; John Wiley & Sons: New York, 1996; Vol. 4; http://dx.doi.org/10.1002/0470034351 PMid:9012996
- (1996) The Chemistry of Organophosphorus Compounds , vol.4
- Hartley, F.R.¹

26
- 0004231121
- John Wiley & Sons: New York
- (c) Quin, L. D., Ed. A Guide to Organophosphorus Chemistry; John Wiley & Sons: New York, 2000;
- (2000) A Guide to Organophosphorus Chemistry
- Quin, L.D.¹

27
- 0000468730
- (d) Mader, M. M.; Bartlett, P. A. Chem. Rev. 1997, 97, 1281; http://dx.doi.org/10.1021/cr960435y PMid:11851452
- (1997) Chem. Rev. , vol.97 , pp. 1281
- Mader, M.M.¹ Bartlett, P.A.²

28
- 0016846996
- (e) Brassfield, H. A.; Jacobson, R. A.; Verkade, J. G. J. Am. Chem. Soc. 1975, 97, 4143. http://dx.doi.org/10.1021/ja00847a053.
- (1975) J. Am. Chem. Soc. , vol.97 , pp. 4143
- Brassfield, H.A.¹ Jacobson, R.A.² Verkade, J.G.³

29
- 0001120995
- (f) Darrow, J. W.; Drueckhammer, D. G. J. Org. Chem. 1994, 59, 2976; http://dx.doi.org/10.1021/jo00090a014.
- (1994) J. Org. Chem. , vol.59 , pp. 2976
- Darrow, J.W.¹ Drueckhammer, D.G.²

30
- 2342627551
- Agrotech Publishing Academy Press: Udaipur India
- (g) Cupta, H. C. L. Insecticides: Toxicology and Uses; Agrotech Publishing Academy Press: Udaipur (India), 1999, p 51211;
- (1999) Insecticides: Toxicology and Uses , pp. 51211
- Cupta, H.C.L.¹

31
- 0003892312
- nd ed.; New York: Plenum Press
- nd ed.; New York: Plenum Press, 1985, pp 62-90. http://dx.doi.org/10.1007/978-1-4613-2491-1
- (1985) Toxicology of Insecticides , pp. 62-90
- Matsumura, F.¹

32
- 4544371662
- For the synthetic routes of NHC precursors, see: (a) Pesch, J.; Harms, K.; Bach, T. Eur. J. Org. Chem. 2004, 2025-2035; http://dx.doi.org/10.1002/ejoc. 200300762
- (2004) Eur. J. Org. Chem. , pp. 2025-2035
- Pesch, J.¹ Harms, K.² Bach, T.³

33
- 0024639639
- (b) Van Den Berg, H. J.; Challa, G.; Pandit, U. K. J. Molecular Catal. 1989, 51, 1-12; http://dx.doi.org/10.1016/0304-5102 (89) 87003-8.
- (1989) J. Molecular Catal. , vol.51 , pp. 1-12
- Van Den Berg, H.J.¹ Challa, G.² Pandit, U.K.³

34
- 22144480983
- (c) Kerr, M. S.; Read de Alaniz, J.; Rovis, T. J. Org. Chem. 2005, 70, 5725-5728; http://dx.doi.org/10.1021/jo050645n PMid:15989360 PMCid:2527449.
- (2005) J. Org. Chem. , vol.70 , pp. 5725-5728
- Kerr, M.S.¹ Read De Alaniz, J.² Rovis, T.³

35
- 0033579627
- (d) Arduengo, A. J.; Krafczyk, R.; Schmutzler, R.; Craig, H. A.; Goerlich, J. R.; Marshall, W. J.; Unverzagt, M. Tetrahedron 1999, 55, 14523-14534. http://dx.doi.org/10.1016/S0040-4020 (99) 00927-8
- (1999) Tetrahedron , vol.55 , pp. 14523-14534
- Arduengo, A.J.¹ Krafczyk, R.² Schmutzler, R.³ Craig, H.A.⁴ Goerlich, J.R.⁵ Marshall, W.J.⁶ Unverzagt, M.⁷

36
- 0347870368
- (e) Enders, D.; Gielen, H. J. Organomet. Chem. 2001, 617-618, 70-80; http://dx.doi.org/10.1016/S0022-328X (00) 00600-8
- (2001) Organomet. Chem. , vol.617-618 , pp. 70-80
- Enders, D.¹ Gielen, H.J.²

37
- 33745150697
- (f) Jazzar, R.; Liang, H. Z.; Donnadieu, B.; Bertrand, G. J. Organomet. Chem. 2006, 691, 3201-3205; http://dx.doi.org/10.1016/j.jorganchem.2006.04.008 PMid:19543436 PMCid:2699275.
- (2006) J. Organomet. Chem. , vol.691 , pp. 3201-3205
- Jazzar, R.¹ Liang, H.Z.² Donnadieu, B.³ Bertrand, G.⁴

38
- 41349116270
- (g) Matsuoka, Y.; Ishida, Y.; Saigo, K. Tetrahedron Lett. 2008, 49, 2985-2989. http://dx.doi.org/10.1016/j.tetlet.2008.02.175
- (2008) Tetrahedron Lett. , vol.49 , pp. 2985-2989
- Matsuoka, Y.¹ Ishida, Y.² Saigo, K.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.