SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Organic Chemistry Frontiers

Volumn 1, Issue 3, 2014, Pages 289-293

Palladium-catalyzed cascade cyclization for the construction of spiro-N,O-acetals

(3) Cheng, Jiashun a Chen, Pinhong a Liu, Guosheng a

a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; CATALYSIS; KETONES; ORGANIC ACIDS; PALLADIUM;

CASCADE CYCLIZATION; PALLADIUM-CATALYZED; PYRUVIC ACID;

CYCLIZATION;

EID: 84907739086 PISSN: 20524110 EISSN: 20524129 Source Type: Journal
DOI: 10.1039/c4qo00002a Document Type: Article

Times cited : (7)

References (38)

1
- 0003624033
- Academic, New York
- R. F. Heck, Palladium Reagents in Organic Synthesis, Academic, New York, 1985
- (1985) Palladium Reagents in Organic Synthesis
- Heck, R.F.¹

2
- 84956794765
- Wiley-VCH, Weinheim
- A. Ricci, Modern Amination Methods, Wiley-VCH, Weinheim, 2000
- (2000) Modern Amination Methods
- Ricci, A.¹

3
- 0004220870
- Wiley-VCH, Weinheim
- K. C. Nicolaou and E. J. Sorensen, Classics in Total Synthesis: Targets, Strategies, Methods, Wiley-VCH, Weinheim, 1996
- (1996) Classics in Total Synthesis: Targets, Strategies, Methods
- Nicolaou, K.C.¹ Sorensen, E.J.²

4
- 0003995267
- John Wiley & Sons, New York
- E. Negishi, Handbook of Organopalladium Chemistry for Organic Synthesis, John Wiley & Sons, New York, 2002
- (2002) Handbook of Organopalladium Chemistry for Organic Synthesis
- Negishi, E.¹

5
- 0003417469
- Pergamon, Oxford
- B. M. Trost and I. Fleming, Comprehensive Organic Synthesis, Pergamon, Oxford, 1991
- (1991) Comprehensive Organic Synthesis
- Trost, B.M.¹ Fleming, I.²

6
- 0016651538
- E. Breuer S. Zbaida Tetrahedron 1975 31 499
- (1975) Tetrahedron , vol.31 , pp. 499
- Breuer, E.¹ Zbaida, S.²

7
- 0008349462
- E. Leete G. B. Bodem J. Am. Chem. Soc. 1976 98 6321
- (1976) J. Am. Chem. Soc. , vol.98 , pp. 6321
- Leete, E.¹ Bodem, G.B.²

8
- 0033591940
- F. He Y. Bo J. D. Altom E. J. Corey J. Am. Chem. Soc. 1999 121 6771
- (1999) J. Am. Chem. Soc. , vol.121 , pp. 6771
- He, F.¹ Bo, Y.² Altom, J.D.³ Corey, E.J.⁴

9
- 70349978073
- K. C. Nicolaou S. M. Dalby S. Li T. Suzuki D. Y.-K. Chen Angew. Chem., Int. Ed. 2009 48 7616
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 7616
- Nicolaou, K.C.¹ Dalby, S.M.² Li, S.³ Suzuki, T.⁴ Chen, D.Y.-K.⁵

10
- 84870063162
- H. Satoh H. Ueda H. Tokuyama Tetrahedron 2013 69 89
- (2013) Tetrahedron , vol.69 , pp. 89
- Satoh, H.¹ Ueda, H.² Tokuyama, H.³

11
- 0141594838
- S. Sumi K. Matsumoto H. Tokuyama T. Fukuyama Tetrahedron 2003 59 8571
- (2003) Tetrahedron , vol.59 , pp. 8571
- Sumi, S.¹ Matsumoto, K.² Tokuyama, H.³ Fukuyama, T.⁴

12
- 84859804827
- S. Naud S. J. Macnaughton B. S. Dyson D. J. Woollaston J. W. P. Dallimore J. Robertson Org. Biomol. Chem. 2012 10 3506
- (2012) Org. Biomol. Chem. , vol.10 , pp. 3506
- Naud, S.¹ Macnaughton, S.J.² Dyson, B.S.³ Woollaston, D.J.⁴ Dallimore, J.W.P.⁵ Robertson, J.⁶

13
- 0000407254
- J. L. Bullington J. H. Dodd J. Heterocycl. Chem. 1998 35 397
- (1998) J. Heterocycl. Chem. , vol.35 , pp. 397
- Bullington, J.L.¹ Dodd, J.H.²

14
- 70450175268
- T. Wu G. Yin G. Liu J. Am. Chem. Soc. 2009 131 16354
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 16354
- Wu, T.¹ Yin, G.² Liu, G.³

15
- 84883326763
- For the X-ray structure of 3n and 3o, see the Supporting Information
- T. Wu J. Cheng P. Chen G. Liu Chem. Commun. 2013 49 8707
- (2013) Chem. Commun. , vol.49 , pp. 8707
- Wu, T.¹ Cheng, J.² Chen, P.³ Liu, G.⁴

16
- 42649144150
- J. Liu Z. Yang Z. Wang F. Wang X. Chen X. Liu X. Feng Z. Su C. Hu J. Am. Chem. Soc. 2008 130 5654
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 5654
- Liu, J.¹ Yang, Z.² Wang, Z.³ Wang, F.⁴ Chen, X.⁵ Liu, X.⁶ Feng, X.⁷ Su, Z.⁸ Hu, C.⁹

17
- 79960328309
- X. Zhu A. Lin L. Fang W. Li C. Zhu Y. Cheng Chem.-Eur. J. 2011 17 8281
- (2011) Chem.-Eur. J. , vol.17 , pp. 8281
- Zhu, X.¹ Lin, A.² Fang, L.³ Li, W.⁴ Zhu, C.⁵ Cheng, Y.⁶

18
- 37549072291
- X. Xu Z. Tang Y. Wang S. Luo L. Cun L. Gong J. Org. Chem. 2007 72 9905
- (2007) J. Org. Chem. , vol.72 , pp. 9905
- Xu, X.¹ Tang, Z.² Wang, Y.³ Luo, S.⁴ Cun, L.⁵ Gong, L.⁶

19
- 84985257191
- A. Bender D. Gtlnther R. Wingen Liebigs Ann. Chem. 1985 579
- (1985) Liebigs Ann. Chem. , pp. 579
- Bender, A.¹ Gtlnther, D.² Wingen, R.³

20
- 0041302074
- R. B. Salem G. Jenner Tetrahedron Lett. 1986 27 1575
- (1986) Tetrahedron Lett. , vol.27 , pp. 1575
- Salem, R.B.¹ Jenner, G.²

21
- 85057923465
- A
- P. Wang and W. J. Asbell, Patent, US4968812 A, 1990
- (1990) Patent , pp. US4968812
- Wang, P.¹ Asbell, W.J.²

22
- 84877695159
- J. S. Yadav K. V. Raghavendra Rao A. Kavita D. K. Mohapatra Eur. J. Org. Chem. 2013 2849
- (2013) Eur. J. Org. Chem. , pp. 2849
- Yadav, J.S.¹ Raghavendra Rao, K.V.² Kavita, A.³ Mohapatra, D.K.⁴

23
- 84879888367
- L. N. Aldrich C. B. Berry B. S. Bates L. C. Konkol M. So C. W. Lindsley Eur. J. Org. Chem. 2013 4215
- (2013) Eur. J. Org. Chem. , pp. 4215
- Aldrich, L.N.¹ Berry, C.B.² Bates, B.S.³ Konkol, L.C.⁴ So, M.⁵ Lindsley, C.W.⁶

24
- 33847622915
- G. Spagnol A. Rajca S. Rajca J. Org. Chem. 2007 72 1867
- (2007) J. Org. Chem. , vol.72 , pp. 1867
- Spagnol, G.¹ Rajca, A.² Rajca, S.³

25
- 79955115593
- Y. Fu F. Ye W. Xu Heterocycl. Commun. 2010 16 43
- (2010) Heterocycl. Commun. , vol.16 , pp. 43
- Fu, Y.¹ Ye, F.² Xu, W.³

26
- 0003690482
- D. Reidel, Dordrecht, Holland, p.
- P. M. Henry, Palladium Catalyzed Oxidation of Hydrocarbons, D. Reidel, Dordrecht, Holland, 1980, p. 41
- (1980) Palladium Catalyzed Oxidation of Hydrocarbons , pp. 41
- Henry, P.M.¹

27
- 84939516517
- in, ed. E. Negishi, Wiley & Sons, New York, p. The reaction of N-Me- afforded allylic acetoxylation product in 93% yield with a 2.3 : 1 linear : branch ratio. For selective examples
- P. M. Henry, in Handbook of Organopalladium Chemistry for Organic Synthesis, ed., E. Negishi, Wiley & Sons, New York, 2001, p. 209
- (2001) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.1 , pp. 209
- Henry, P.M.¹

28
- 79952149247
- Y. Wu G. Liu Top. Curr. Chem. 2010 292 195
- (2010) Top. Curr. Chem. , vol.292 , pp. 195
- Wu, Y.¹ Liu, G.²

29
- 1042276609
- M. S. Chen M. C. White J. Am. Chem. Soc. 2004 126 1346
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 1346
- Chen, M.S.¹ White, M.C.²

30
- 78049392925
- When some simple alkenes, such as styrene and 1-octene, were treated under standard reaction conditions, no ketone products were observed. These results are also against the Wacker process pathway
- A. N. Campell P. B. White I. A. Guzei S. S. Stahl J. Am. Chem. Soc. 2010 132 15116
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 15116
- Campell, A.N.¹ White, P.B.² Guzei, I.A.³ Stahl, S.S.⁴

31
- 34047161855
- V. Kotov C. C. Scarborough S. S. Stahl Inorg. Chem. 2007 46 1910
- (2007) Inorg. Chem. , vol.46 , pp. 1910
- Kotov, V.¹ Scarborough, C.C.² Stahl, S.S.³

32
- 35548990249
- M. M. Rogers V. Kotov J. Chatwichien S. S. Stahl Org. Lett. 2007 9 4331
- (2007) Org. Lett. , vol.9 , pp. 4331
- Rogers, M.M.¹ Kotov, V.² Chatwichien, J.³ Stahl, S.S.⁴

33
- 84857828738
- J. E. Redford R. I. McDonald M. L. Rigsby J. D. Wiensch S. S. Stahl Org. Lett. 2012 14 1242
- (2012) Org. Lett. , vol.14 , pp. 1242
- Redford, J.E.¹ McDonald, R.I.² Rigsby, M.L.³ Wiensch, J.D.⁴ Stahl, S.S.⁵

34
- 84886772942
- A. B. Weinstein D. P. Schuman Z. X. Tan S. S. Stahl Angew. Chem., Int. Ed. 2013 52 11867
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 11867
- Weinstein, A.B.¹ Schuman, D.P.² Tan, Z.X.³ Stahl, S.S.⁴

35
- 33645463109
- The low conversion is possibly due to the exhaustion of benzoyl-formic acid 2a, which reacted with 4a to give 3a
- F. E. Michael B. M. Cochran J. Am. Chem. Soc. 2006 128 4246
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 4246
- Michael, F.E.¹ Cochran, B.M.²

36
- 33947461753
- P. J. A. Demoen P. A. J. Janssen J. L. M. Loomans J. Am. Chem. Soc. 1959 81 6286
- (1959) J. Am. Chem. Soc. , vol.81 , pp. 6286
- Demoen, P.J.A.¹ Janssen, P.A.J.² Loomans, J.L.M.³

37
- 0014519150
- D. H. R. Barton N. J. A. Gutteridge R. H. Hesse M. M. Pechet J. Org. Chem. 1969 34 1473
- (1969) J. Org. Chem. , vol.34 , pp. 1473
- Barton, D.H.R.¹ Gutteridge, N.J.A.² Hesse, R.H.³ Pechet, M.M.⁴

38
- 0034815686
- H.-Y. Lee Y.-H. Lee Synlett 2001 1656
- (2001) Synlett , pp. 1656
- Lee, H.-Y.¹ Lee, Y.-H.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.