SCOPUS 정보 검색 플랫폼

Volumn , Issue 24, 2009, Pages 3594-3596

Furans versus 4H-pyrans: Catalyst-controlled regiodivergent tandem Michael addition-cyclization reaction of 2-(1-alkynyl)-2-alken-1-ones with 1,3-dicarbonyl compounds

(2) Xiao, Yuanjing a Zhang, Junliang a,b

a EAST CHINA NORMAL UNIVERSITY (China)

b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY (China)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DICARBONYL COMPOUND; 1,8 DIAZABICYCLO[5.4.0]UNDECEN 7 ENE; 2 (1 ALKYNYL) 2 ALKEN 1 ESTER DERIVATIVE; ACETYLACETONE; ALKENE DERIVATIVE; CARBONYL DERIVATIVE; ESTER DERIVATIVE; FURAN DERIVATIVE; PALLADIUM; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CYCLIZATION; MICHAEL ADDITION; SYNTHESIS;

EID: 67650596682 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b905267d Document Type: Article

Times cited : (77)

References (37)

1
- 0003851576
- John Wiley & Sons, Chichester
- A. F. Pozharskii, A. T. Soldatenkov and A. R. Katritzky, in Heterocycles in Life and Society, John Wiley & Sons, Chichester, 1997
- (1997) Heterocycles in Life and Society
- Pozharskii, A.F.¹ Soldatenkov, A.T.² Katritzky In, A.R.³

2
- 48249096215
- Synapse Information Resources, Inc, New York
- M. Ash and I. Ash, in Handbook of Flavors and Fragrances, Synapse Information Resources, Inc, New York, 2006
- (2006) Handbook of Flavors and Fragrances
- Ash, M.¹ Ash In, I.²

3
- 14644421556
- H.-K. Lee K.-F. Chan C.-W. Hui H.-K. Yim X.- W. Wu H. N. C. Wong Pure Appl. Chem. 2005 77 139
- (2005) Pure Appl. Chem. , vol.77 , pp. 139
- Lee, H.-K.¹ Chan, K.-F.² Hui, C.-W.³ Yim, H.-K.⁴ Wu -, X.W.⁵ Wong, H.N.C.⁶

4
- 0004220870
- VCH, Weinheim, Germany
- K. C. Nicolaou and E. J. Sorensen, Classics in Total Synthesis, VCH, Weinheim, Germany, 1996
- (1996) Classics in Total Synthesis
- Nicolaou, K.C.¹ Sorensen, E.J.²

5
- 0038487765
- K. Urbahns E. Horváth J.-P. Stasch F. Mauler Bioorg. Med. Chem. Lett. 2003 13 2637
- (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 2637
- Urbahns, K.¹ Horváth, E.² Stasch, J.-P.³ Mauler, F.⁴

6
- 0034747199
- B. S. Jensen D. Strobaek S. P. Olesen P. Christophersen Curr. Drug Targets 2001 2 401
- (2001) Curr. Drug Targets , vol.2 , pp. 401
- Jensen, B.S.¹ Strobaek, D.² Olesen, S.P.³ Christophersen, P.⁴

7
- 16244369402
- For recent reviews, accounts, and highlights dealing with the synthesis of furans since 2005, see:
- R. Kohler H. Wulff I. Eichler M. Kneifel D. Neumann A. Knorr I. Grgic D. Kampfe H. Si J. Wibawa R. Real K. Borner S. Brakemeier H. D. Orzechowski H. P. Reusch M. Paul K. G. Chandy J. Hoyer Circulation 2003 108 1119
- (2003) Circulation , vol.108 , pp. 1119
- Kohler, R.¹ Wulff, H.² Eichler, I.³ Kneifel, M.⁴ Neumann, D.⁵ Knorr, A.⁶ Grgic, I.⁷ Kampfe, D.⁸ Si, H.⁹ Wibawa, J.¹⁰ Real, R.¹¹ Borner, K.¹² Brakemeier, S.¹³ Orzechowski, H.D.¹⁴ Reusch, H.P.¹⁵ Paul, M.¹⁶ Chandy, K.G.¹⁷ Hoyer, J.¹⁸

8
- 13744249187
- R. C. D. Brown Angew. Chem., Int. Ed. 2005 44 850
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 850
- Brown, R.C.D.¹

9
- 33744802336
- S. F. Kirsch Org. Biomol. Chem. 2006 4 2076
- (2006) Org. Biomol. Chem. , vol.4 , pp. 2076
- Kirsch, S.F.¹

10
- 34250627489
- D. M. D'Souza T. J. J. Müller Chem. Soc. Rev. 2007 36 1095
- (2007) Chem. Soc. Rev. , vol.36 , pp. 1095
- D'Souza, D.M.¹ Müller, T.J.J.²

11
- 33847309847
- N. T. Patil Y. Yamamoto ARKIVOC 2007 (x) 121
- (2007) ARKIVOC , vol.10 , pp. 121
- Patil, N.T.¹ Yamamoto, Y.²

12
- 45249087881
- G. Balme D. Bouyssi N. Monteiro Heterocycles 2007 73 87
- (2007) Heterocycles , vol.73 , pp. 87
- Balme, G.¹ Bouyssi, D.² Monteiro, N.³

13
- 42049119869
- G. W. Gribble and J. A. Joule, Pergamon, Oxford, p. 176
- X. L. Hou, Z. Yang, K.-S. Y and H. N. C. Wong, in Progress in Heterocyclic Chemistry, ed., G. W. Gribble, and, J. A. Joule, Pergamon, Oxford, 2008, vol. 19, p. 176
- (2008) Progress in Heterocyclic Chemistry, Ed.
- Hou, X.L.¹ Yang, Z.² Wong, H.N.C.³

14
- 55349083675
- For recent literature and patents dealing with the synthesis of pyrans, see:
- S. F. Kirsch Synthesis 2008 3183
- (2008) Synthesis , pp. 3183
- Kirsch, S.F.¹

15
- 33645391803
- A. John P. J. P. Yadav S. Palaniappan J. Mol. Catal. A: Chem. 2006 248 121
- (2006) J. Mol. Catal. A: Chem. , vol.248 , pp. 121
- John, A.¹ Yadav, P.J.P.² Palaniappan, S.³

16
- 34248223139
- G. I. Shakibaei P. Mirzaei A. Bazgir Appl. Catal., A 2007 325 188
- (2007) Appl. Catal., A , vol.325 , pp. 188
- Shakibaei, G.I.¹ Mirzaei, P.² Bazgir, A.³

17
- 33644599352
- B. Das P. Thirupathi I. Mahender V. S. Reddy Y. K. Rao J. Mol. Catal. A: Chem. 2006 247 233
- (2006) J. Mol. Catal. A: Chem. , vol.247 , pp. 233
- Das, B.¹ Thirupathi, P.² Mahender, I.³ Reddy, V.S.⁴ Rao, Y.K.⁵

18
- 67650622757
- EP 0758648
- EP 0758648

19
- 21244479265
- S. Kamijo C. Kanazawa Y. Yamamoyo J. Am. Chem. Soc. 2005 127 9260
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 9260
- Kamijo, S.¹ Kanazawa, C.² Yamamoyo, Y.³

20
- 34548654368
- B. Alcaide P. Almendros T. Martínez del Campo Angew. Chem., Int. Ed. 2007 46 6684
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 6684
- Alcaide, B.¹ Almendros, P.² Martínez Del Campo, T.³

21
- 35948975670
- S. Chuprakov V. Gevorgyan Org. Lett. 2007 9 4463
- (2007) Org. Lett. , vol.9 , pp. 4463
- Chuprakov, S.¹ Gevorgyan, V.²

22
- 38649108487
- A. S. Dudnik A. W. Sromek M. Rubina J. T. Kim A. V. Kel'in V. Gevorgyan J. Am. Chem. Soc. 2008 130 1440
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 1440
- Dudnik, A.S.¹ Sromek, A.W.² Rubina, M.³ Kim, J.T.⁴ Kel'In, A.V.⁵ Gevorgyan, V.⁶

23
- 53949089396
- X. Jiang X. Ma Z. Zheng S. Ma Chem.-Eur. J. 2008 14 8572
- (2008) Chem.-Eur. J. , vol.14 , pp. 8572
- Jiang, X.¹ Ma, X.² Zheng, Z.³ Ma, S.⁴

24
- 58549084996
- H. Gao J. Zhang Adv. Synth. Catal. 2009 351 85
- (2009) Adv. Synth. Catal. , vol.351 , pp. 85
- Gao, H.¹ Zhang, J.²

25
- 53849093807
- X. Yu H. Ren Y. Xiao J. Zhang Chem.-Eur. J. 2008 14 8481
- (2008) Chem.-Eur. J. , vol.14 , pp. 8481
- Yu, X.¹ Ren, H.² Xiao, Y.³ Zhang, J.⁴

26
- 41949130150
- Y. Xiao J. Zhang Angew. Chem., Int. Ed. 2008 47 1903
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 1903
- Xiao, Y.¹ Zhang, J.²

27
- 62549125065
- Y. Xiao J. Zhang Adv. Synth. Catal. 2009 351 617
- (2009) Adv. Synth. Catal. , vol.351 , pp. 617
- Xiao, Y.¹ Zhang, J.²

28
- 0037434118
- S. Ma J. Zhang Angew. Chem., Int. Ed. 2003 42 184
- (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 184
- Ma, S.¹ Zhang, J.²

29
- 3543138426
- 3, see:
- S. Ma L. Lu J. Zhang J. Am. Chem. Soc. 2004 126 9645
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 9645
- Ma, S.¹ Lu, L.² Zhang, J.³

30
- 4544255270
- For reviews, see:
- T. Yao X. Zhang R. C. Larock J. Am. Chem. Soc. 2004 126 11164
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 11164
- Yao, T.¹ Zhang, X.² Larock, R.C.³

31
- 33644543398
- M. Sodeoka Y. Hamashima Pure Appl. Chem. 2006 78 477
- (2006) Pure Appl. Chem. , vol.78 , pp. 477
- Sodeoka, M.¹ Hamashima, Y.²

32
- 21244459544
- M. Sodeoka Y. Hamashima Bull. Chem. Soc. Jpn. 2005 78 941
- (2005) Bull. Chem. Soc. Jpn. , vol.78 , pp. 941
- Sodeoka, M.¹ Hamashima, Y.²

33
- 16244364063
- -1529
- Y. Hamashima N. Sasamoto D. Hotta H. Somei N. Umebayashi M. Sodeoka Angew. Chem., Int. Ed. 2005 44 1525 1529
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 1525
- Hamashima, Y.¹ Sasamoto, N.² Hotta, D.³ Somei, H.⁴ Umebayashi, N.⁵ Sodeoka, M.⁶

34
- 34547210299
- I. Fukuchi Y. Hamashima M. Sodeoka Adv. Synth. Catal. 2007 349 509
- (2007) Adv. Synth. Catal. , vol.349 , pp. 509
- Fukuchi, I.¹ Hamashima, Y.² Sodeoka, M.³

35
- 53549115640
- N. Umebayashi Y. Hamashima M. Sodeoka Angew. Chem., Int. Ed. 2008 47 4196
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4196
- Umebayashi, N.¹ Hamashima, Y.² Sodeoka, M.³

36
- 33750443223
- TfOH cooperatively activates the enone see:
- N. Sasamoto C. Dubs Y. Hamashima M. Sodeoka J. Am. Chem. Soc. 2006 128 14010
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 14010
- Sasamoto, N.¹ Dubs, C.² Hamashima, Y.³ Sodeoka, M.⁴

37
- 27544474635
- Y. Hamashima D. Hotta N. Umebayashi Y. Tsuchiya T. Suzuki M. Sodeoka Adv. Synth. Catal. 2005 347 1576
- (2005) Adv. Synth. Catal. , vol.347 , pp. 1576
- Hamashima, Y.¹ Hotta, D.² Umebayashi, N.³ Tsuchiya, Y.⁴ Suzuki, T.⁵ Sodeoka, M.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.