SCOPUS 정보 검색 플랫폼

European Journal of Organic Chemistry

Volumn 2014, Issue 14, 2014, Pages 3001-3008

Heck, Sonogashira, and Hiyama reactions catalyzed by palladium nanoparticles stabilized by tris-imidazolium salt

(6) Planellas, Marc a Moglie, Yanina b Alonso, Francisco b Yus, Miguel b Pleixats, Roser a Shafir, Alexandr a

a UNIVERSITAT AUTÒNOMA DE BARCELONA (Spain)

b UNIVERSITY OF ALICANTE (Spain)

Author keywords

Cross coupling; Heterogeneous catalysis; Nanoparticles; Palladium

Indexed keywords

EID: 84899928481 PISSN: 1434193X EISSN: 10990690 Source Type: Journal
DOI: 10.1002/ejoc.201400162 Document Type: Article

Times cited : (28)

References (77)

1
- 78649571535
- Angew. Chem. 2010, 122, 9231-9234
- X.-F. Wu, P. Anbarasan, H. Neumann, M. Beller, Angew. Chem. Int. Ed. 2010, 49, 9047-9050; Angew. Chem. 2010, 122, 9231-9234.
- (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9047-9050
- Wu, X.-F.¹ Anbarasan, P.² Neumann, H.³ Beller, M.⁴

2
- 84862065162
- Angew. Chem. 2012, 124, 5150-5174
- C. C. C. Johansson Seechurn, M. O. Kitching, T. J. Colacot, V. Snieckus, Angew. Chem. Int. Ed. 2012, 51, 5062-5085; Angew. Chem. 2012, 124, 5150-5174.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5062-5085
- Johansson Seechurn, C.C.C.¹ Kitching, M.O.² Colacot, T.J.³ Snieckus, V.⁴

3
- 84899917805
- For some reviews dealing with the Heck reaction and its applications, see
- For some reviews dealing with the Heck reaction and its applications, see

4
- 0034249671
- I. P. Beletskaya, A. V. Cheprakov, Chem. Rev. 2000, 100, 3009-3066.
- (2000) Chem. Rev. , vol.100 , pp. 3009-3066
- Beletskaya, I.P.¹ Cheprakov, A.V.²

5
- 0035959456
- N. J. Whitcombe, K. K. Hii, S. E. Gibson, Tetrahedron 2001, 57, 7449-7476.
- (2001) Tetrahedron , vol.57 , pp. 7449-7476
- Whitcombe, N.J.¹ Hii, K.K.² Gibson, S.E.³

6
- 27844611214
- F. Alonso, I. P. Beletskaya, M. Yus, Tetrahedron 2005, 61, 11771-11835.
- (2005) Tetrahedron , vol.61 , pp. 11771-11835
- Alonso, F.¹ Beletskaya, I.P.² Yus, M.³

7
- 33751284543
- A. F. Schmidt, A. Al Halaiqa, V. V. Smirnov, Synlett 2006, 2861-2878.
- (2006) Synlett , pp. 2861-2878
- Schmidt, A.F.¹ Al Halaiqa, A.² Smirnov, V.V.³

8
- 33845536463
- J. P. Knowles, A. Whiting, Org. Biomol. Chem. 2007, 5, 31-44.
- (2007) Org. Biomol. Chem. , vol.5 , pp. 31-44
- Knowles, J.P.¹ Whiting, A.²

9
- 33847019589
- A. M. Trzeciak, J. J. Ziõłkowski, Coord. Chem. Rev. 2007, 251, 1281-1293.
- (2007) Coord. Chem. Rev. , vol.251 , pp. 1281-1293
- Trzeciak, A.M.¹ Ziõłkowski, J.J.²

10
- 80054980226
- D. McCartney, P. J. Guiry, Chem. Soc. Rev. 2011, 40, 5122-5150.
- (2011) Chem. Soc. Rev. , vol.40 , pp. 5122-5150
- McCartney, D.¹ Guiry, P.J.²

11
- 84899940059
- For selected reviews dealing with the Sonogashira reaction and its applications, see
- For selected reviews dealing with the Sonogashira reaction and its applications, see

12
- 0038675906
- Sonogashira Alkyne Synthesis
- (Eds.:, Wiley-Interscience, New York, chapter III.2.8.1
- K. Sonogashira, Sonogashira Alkyne Synthesis in: Handbook of Organopalladium Chemistry for Organic Synthesis (Eds.:, E. Negishi, A. de Meijere), Wiley-Interscience, New York, 2002, vol. I, chapter III.2.8.1, p. 493-529.
- (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , pp. 493-529
- Sonogashira, K.¹ Negishi, E.² De Meijere, A.³

13
- 0037943974
- E. Negishi, L. Anastasia, Chem. Rev. 2003, 103, 1979-2017.
- (2003) Chem. Rev. , vol.103 , pp. 1979-2017
- Negishi, E.¹ Anastasia, L.²

14
- 33947727055
- R. Chinchilla, C. Nájera, Chem. Rev. 2007, 107, 874-922.
- (2007) Chem. Rev. , vol.107 , pp. 874-922
- Chinchilla, R.¹ Nájera, C.²

15
- 33846688751
- Angew. Chem. 2007, 119, 850-888
- H. Doucet, J.-C. Hierso, Angew. Chem. Int. Ed. 2007, 46, 834-871; Angew. Chem. 2007, 119, 850-888.
- (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 834-871
- Doucet, H.¹ Hierso, J.-C.²

16
- 80052592184
- R. Chinchilla, C. Nájera, Chem. Soc. Rev. 2011, 40, 5084-5121.
- (2011) Chem. Soc. Rev. , vol.40 , pp. 5084-5121
- Chinchilla, R.¹ Nájera, C.²

17
- 84899914529
- For selected reviews dealing with the Suzuki coupling and its applications, see
- For selected reviews dealing with the Suzuki coupling and its applications, see

18
- 0346786657
- A. Suzuki, J. Organomet. Chem. 1999, 576, 147-168.
- (1999) J. Organomet. Chem. , vol.576 , pp. 147-168
- Suzuki, A.¹

19
- 0035905441
- Angew. Chem. 2001, 113, 4676
- S. R. Chemler, D. Trauner, S. J. Danishefsky, Angew. Chem. Int. Ed. 2001, 40, 4544-4568; Angew. Chem. 2001, 113, 4676.
- (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 4544-4568
- Chemler, S.R.¹ Trauner, D.² Danishefsky, S.J.³

20
- 0037175592
- S. Kotha, K. Lahiri, D. Kashinath, Tetrahedron 2002, 58, 9633-9695.
- (2002) Tetrahedron , vol.58 , pp. 9633-9695
- Kotha, S.¹ Lahiri, K.² Kashinath, D.³

21
- 7644241634
- F. Bellina, A. Carpita, R. Rossi, Synthesis 2004, 2419-2440.
- (2004) Synthesis , pp. 2419-2440
- Bellina, F.¹ Carpita, A.² Rossi, R.³

22
- 39749179066
- F. Alonso, I. P. Beletskaya, M. Yus, Tetrahedron 2008, 64, 3047-3101.
- (2008) Tetrahedron , vol.64 , pp. 3047-3101
- Alonso, F.¹ Beletskaya, I.P.² Yus, M.³

23
- 72949108920
- Angew. Chem. 2009, 121, 9404-9425
- G. A. Molander, B. Canturk, Angew. Chem. Int. Ed. 2009, 48, 9240-9261; Angew. Chem. 2009, 121, 9404-9425.
- (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9240-9261
- Molander, G.A.¹ Canturk, B.²

24
- 84866742794
- M. M. Heravi, E. Hashemi, Tetrahedron 2012, 68, 9145-9178.
- (2012) Tetrahedron , vol.68 , pp. 9145-9178
- Heravi, M.M.¹ Hashemi, E.²

25
- 84899955399
- For selected recent reviews on the palladium-catalyzed cross-coupling of organosilicon reagents, see
- For selected recent reviews on the palladium-catalyzed cross-coupling of organosilicon reagents, see

26
- 80055021902
- Y. Nakao, T. Hiyama, Chem. Soc. Rev. 2011, 40, 4893-4901.
- (2011) Chem. Soc. Rev. , vol.40 , pp. 4893-4901
- Nakao, Y.¹ Hiyama, T.²

27
- 84856899190
- W. R. J. D. Galloway
- H. F. Sore, W. R. J. D. Galloway, D. R. Spring, Chem. Soc. Rev. 2012, 41, 1845-1866.
- (2012) Chem. Soc. Rev. , vol.41 , pp. 1845-1866
- Sore, H.F.¹ Spring, D.R.²

28
- 22744442306
- Angew. Chem. 2005, 117, 4516-4563
- K. C. Nicolaou, P. G. Bulger, D. Sarlah, Angew. Chem. Int. Ed. 2005, 44, 4442-4489; Angew. Chem. 2005, 117, 4516-4563.
- (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4442-4489
- Nicolaou, K.C.¹ Bulger, P.G.² Sarlah, D.³

29
- 12344330371
- H.-U. Blaser, A. Indolese, F. Naud, U. Nettekoven, A. Schnyder, Adv. Synth. Catal. 2004, 346, 1583-1598.
- (2004) Adv. Synth. Catal. , vol.346 , pp. 1583-1598
- Blaser, H.-U.¹ Indolese, A.² Naud, F.³ Nettekoven, U.⁴ Schnyder, A.⁵

30
- 33747071481
- J.-P. Corbet, G. Mignani, Chem. Rev. 2006, 106, 2651-2710.
- (2006) Chem. Rev. , vol.106 , pp. 2651-2710
- Corbet, J.-P.¹ Mignani, G.²

31
- 73449103586
- C. Toborg, M. Beller, Adv. Synth. Catal. 2009, 351, 3027-3043.
- (2009) Adv. Synth. Catal. , vol.351 , pp. 3027-3043
- Toborg, C.¹ Beller, M.²

32
- 80052054192
- C. A. Busacca, D. R. Fandrick, J. J. Song, C. H. Senanayake, Adv. Synth. Catal. 2011, 353, 1825-1864.
- (2011) Adv. Synth. Catal. , vol.353 , pp. 1825-1864
- Busacca, C.A.¹ Fandrick, D.R.² Song, J.J.³ Senanayake, C.H.⁴

33
- 4243533879
- Synthesis of Conjugated Polymers for Materials Science
- (Eds.:, Wiley-Interscience, New York, chapter III.2.17.2
- A. D. Schlüter, Z. Bo, Synthesis of Conjugated Polymers for Materials Science, in: Handbook of Organopalladium Chemistry for Organic Synthesis (Eds.:, E. Negishi, A. de Meijere), Wiley-Interscience, New York, 2002, vol. I, chapter III.2.17.2, p. 825-861.
- (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , pp. 825-861
- Schlüter, A.D.¹ Bo, Z.² Negishi, E.³ De Meijere, A.⁴

34
- 80052476041
- M. Hoyos, M. L. Turner, O. Navarro, Curr. Org. Chem. 2011, 15, 3263-3290.
- (2011) Curr. Org. Chem. , vol.15 , pp. 3263-3290
- Hoyos, M.¹ Turner, M.L.² Navarro, O.³

35
- 84899986442
- For catalytic applications of metal nanoparticles, see
- For catalytic applications of metal nanoparticles, see

36
- 84889870520
- (Ed.:, D. Astruc), Wiley-VCH, Weinheim, Germany
- Nanoparticles and Catalysis (Ed.:, D. Astruc), Wiley-VCH, Weinheim, Germany, 2008.
- (2008) Nanoparticles and Catalysis

37
- 0036811253
- A. Roucoux, J. Schulz, H. Patin, Chem. Rev. 2002, 102, 3757-3778.
- (2002) Chem. Rev. , vol.102 , pp. 3757-3778
- Roucoux, A.¹ Schulz, J.² Patin, H.³

38
- 0042975158
- M. Moreno-Mañas, R. Pleixats, Acc. Chem. Res. 2003, 36, 638-643.
- (2003) Acc. Chem. Res. , vol.36 , pp. 638-643
- Moreno-Mañas, M.¹ Pleixats, R.²

39
- 0037448329
- J. A. Widegren, R. G. Finke, J. Mol. Catal. A 2003, 191, 187-207.
- (2003) J. Mol. Catal. A , vol.191 , pp. 187-207
- Widegren, J.A.¹ Finke, R.G.²

40
- 29244458383
- Angew. Chem. 2005, 117, 8062-8083
- D. Astruc, F. Lu, J. Ruiz Aranzaes, Angew. Chem. Int. Ed. 2005, 44, 7852-7872; Angew. Chem. 2005, 117, 8062-8083.
- (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 7852-7872
- Astruc, D.¹ Lu, F.² Ruiz Aranzaes, J.³

41
- 33645347922
- J. G. De Vries, Dalton Trans. 2006, 421-429.
- (2006) Dalton Trans. , pp. 421-429
- De Vries, J.G.¹

42
- 34047185334
- D. Astruc, Inorg. Chem. 2007, 46, 1884-1894.
- (2007) Inorg. Chem. , vol.46 , pp. 1884-1894
- Astruc, D.¹

43
- 84890990371
- (Eds.:, J. G. de Vries, C. J. Elsevier), Wiley-VCH, Weinheim, Germany
- A. Roucoux, K. Philippot, in: Handbook of Homogeneous Hydrogenations (Eds.:, J. G. de Vries, C. J. Elsevier), Wiley-VCH, Weinheim, Germany, 2007, vol. 9, p. 217-256.
- (2007) Handbook of Homogeneous Hydrogenations , vol.9 , pp. 217-256
- Roucoux, A.¹ Philippot, K.²

44
- 51149103482
- A. Corma, H. García, Chem. Soc. Rev. 2008, 37, 2096-2126.
- (2008) Chem. Soc. Rev. , vol.37 , pp. 2096-2126
- Corma, A.¹ García, H.²

45
- 67649133401
- S. Roy, M. A. Pericàs, Org. Biomol. Chem. 2009, 7, 2669-2677.
- (2009) Org. Biomol. Chem. , vol.7 , pp. 2669-2677
- Roy, S.¹ Pericàs, M.A.²

46
- 79956216404
- For a recent review on the use of Pd NPs for C-C coupling reactions, see
- F. Alonso, P. Riente, M. Yus, Acc. Chem. Res. 2011, 44, 379-391. For a recent review on the use of Pd NPs for C-C coupling reactions, see
- (2011) Acc. Chem. Res. , vol.44 , pp. 379-391
- Alonso, F.¹ Riente, P.² Yus, M.³

47
- 80054973153
- A. Balanta, C. Godard, C. Claver, Chem. Soc. Rev. 2011, 40, 4973-4985.
- (2011) Chem. Soc. Rev. , vol.40 , pp. 4973-4985
- Balanta, A.¹ Godard, C.² Claver, C.³

48
- 33847023938
- L. Starkey Ott, R. G. Finke, Coord. Chem. Rev. 2007, 251, 1075-1100.
- (2007) Coord. Chem. Rev. , vol.251 , pp. 1075-1100
- Starkey Ott, L.¹ Finke, R.G.²

49
- 0035969272
- M. Moreno-Mañas, R. Pleixats, S. Villarroya, Organometallics 2001, 20, 4524-4528.
- (2001) Organometallics , vol.20 , pp. 4524-4528
- Moreno-Mañas, M.¹ Pleixats, R.² Villarroya, S.³

50
- 0037033288
- M. Moreno-Mañas, R. Pleixats, S. Villarroya, Chem. Commun. 2002, 60-61.
- (2002) Chem. Commun. , pp. 60-61
- Moreno-Mañas, M.¹ Pleixats, R.² Villarroya, S.³

51
- 33750807508
- A. Serra-Muns, R. Soler, E. Badetti, P. de Mendoza, M. Moreno-Mañas, R. Pleixats, R. M. Sebastián, A. Vallribera, New J. Chem. 2006, 30, 1584-1594.
- (2006) New J. Chem. , vol.30 , pp. 1584-1594
- Serra-Muns, A.¹ Soler, R.² Badetti, E.³ De Mendoza, P.⁴ Moreno-Mañas, M.⁵ Pleixats, R.⁶ Sebastián, R.M.⁷ Vallribera, A.⁸

52
- 70349283131
- N. Mejías, A. Serra-Muns, R. Pleixats, A. Shafir, M. Tristany, Dalton Trans. 2009, 7748-7755.
- (2009) Dalton Trans. , pp. 7748-7755
- Mejías, N.¹ Serra-Muns, A.² Pleixats, R.³ Shafir, A.⁴ Tristany, M.⁵

53
- 77956365303
- N. Mejías, R. Pleixats, A. Shafir, M. Medio-Simõn, G. Asensio, Eur. J. Org. Chem. 2010, 5090-5099.
- (2010) Eur. J. Org. Chem. , pp. 5090-5099
- Mejías, N.¹ Pleixats, R.² Shafir, A.³ Medio-Simõn, M.⁴ Asensio, G.⁵

54
- 84858016909
- M. Planellas, R. Pleixats, A. Shafir, Adv. Synth. Catal. 2012, 354, 651-662.
- (2012) Adv. Synth. Catal. , vol.354 , pp. 651-662
- Planellas, M.¹ Pleixats, R.² Shafir, A.³

55
- 84893976095
- M. Planellas, W. Guo, F. Alonso, M. Yus, A. Shafir, R. Pleixats, T. Parella, Adv. Synth. Catal. 2014, 356, 179-188.
- (2014) Adv. Synth. Catal. , vol.356 , pp. 179-188
- Planellas, M.¹ Guo, W.² Alonso, F.³ Yus, M.⁴ Shafir, A.⁵ Pleixats, R.⁶ Parella, T.⁷

56
- 84899925600
- Few precedents exist on the use of preformed Pd NPs in the Hiyama reaction, see
- Few precedents exist on the use of preformed Pd NPs in the Hiyama reaction, see

57
- 33645456834
- L. Durán Pachõn, M. B. Thathagar, F. Hartl, G. Rothenberg, Phys. Chem. Chem. Phys. 2006, 8, 151-157.
- (2006) Phys. Chem. Chem. Phys. , vol.8 , pp. 151-157
- Durán Pachõn, L.¹ Thathagar, M.B.² Hartl, F.³ Rothenberg, G.⁴

58
- 34548532847
- D. Srimani, S. Sawoo, A. Sarkar, Org. Lett. 2007, 9, 3639-3642.
- (2007) Org. Lett. , vol.9 , pp. 3639-3642
- Srimani, D.¹ Sawoo, S.² Sarkar, A.³

59
- 84860836356
- D. Shah, H. Kaur, J. Mol. Catal. A: Chem. 2012, 359, 69-73.
- (2012) J. Mol. Catal. A: Chem. , vol.359 , pp. 69-73
- Shah, D.¹ Kaur, H.²

60
- 84877051038
- For other examples involving Pd NP generated in situ, see
- A. Grirrane, H. García, A. Corma, J. Catal. 2013, 302, 49-57. For other examples involving Pd NP generated in situ, see
- (2013) J. Catal. , vol.302 , pp. 49-57
- Grirrane, A.¹ García, H.² Corma, A.³

61
- 57449099029
- R. Dey, K. Chattopadhyay, B. C. Ranu, J. Org. Chem. 2008, 73, 9461-9464.
- (2008) J. Org. Chem. , vol.73 , pp. 9461-9464
- Dey, R.¹ Chattopadhyay, K.² Ranu, B.C.³

62
- 42649115108
- B. C. Ranu, R. Dey, K. Chattopadhyay, Tetrahedron Lett. 2008, 49, 3430-3432.
- (2008) Tetrahedron Lett. , vol.49 , pp. 3430-3432
- Ranu, B.C.¹ Dey, R.² Chattopadhyay, K.³

63
- 41849131493
- E. Alacid, C. Nájera, J. Org. Chem. 2008, 73, 2315-2322.
- (2008) J. Org. Chem. , vol.73 , pp. 2315-2322
- Alacid, E.¹ Nájera, C.²

64
- 70349320515
- P. S. Bäuerlein, I. J. S. Fairlamb, A. G. Jarvis, A. F. Lee, C. Müller, J. M. Slattery, R. J. Thatcher, D. Vogt, A. C. Whitwood, Chem. Commun. 2009, 5734-5736.
- (2009) Chem. Commun. , pp. 5734-5736
- Bäuerlein, P.S.¹ Fairlamb, I.J.S.² Jarvis, A.G.³ Lee, A.F.⁴ Müller, C.⁵ Slattery, J.M.⁶ Thatcher, R.J.⁷ Vogt, D.⁸ Whitwood, A.C.⁹

65
- 79955400538
- T. Chatterjee, R. Dey, B. C. Ranu, New J. Chem. 2011, 35, 1103-1110.
- (2011) New J. Chem. , vol.35 , pp. 1103-1110
- Chatterjee, T.¹ Dey, R.² Ranu, B.C.³

66
- 77953530696
- D. Srimani, A. Bej, A. Sarkar, J. Org. Chem. 2010, 75, 4296-4299.
- (2010) J. Org. Chem. , vol.75 , pp. 4296-4299
- Srimani, D.¹ Bej, A.² Sarkar, A.³

67
- 79960265060
- Organometallic Derived Metals, Colloids and Nanoparticles
- (Eds.:, R. H. Crabtree, M. P. Mingos,), Elsevier chapter 12-03
- K. Philippot, B. Chaudret, Organometallic Derived Metals, Colloids and Nanoparticles, in: Comprehensive Organometallic Chemistry III (Eds.:, R. H. Crabtree, M. P. Mingos,), Elsevier, 2007, vol. 12, chapter 12-03, p. 71-99.
- (2007) Comprehensive Organometallic Chemistry III , vol.12 , pp. 71-99
- Philippot, K.¹ Chaudret, B.²

68
- 0000354002
- M. F. Rettig, P. M. Maitlis, Inorg. Synth. 1990, 28, 110-113.
- (1990) Inorg. Synth. , vol.28 , pp. 110-113
- Rettig, M.F.¹ Maitlis, P.M.²

69
- 38349128435
- M. Trilla, R. Pleixats, T. Parella, C. Blanc, P. Dieudonné, Y. Guari, M. Wong Chi Man, Langmuir 2008, 24, 259-265.
- (2008) Langmuir , vol.24 , pp. 259-265
- Trilla, M.¹ Pleixats, R.² Parella, T.³ Blanc, C.⁴ Dieudonné, P.⁵ Guari, Y.⁶ Wong Chi Man, M.⁷

70
- 84899895937
- Palladium-catalyzed reactions of aromatic halides with allylic alcohols leading to the formation of β-aromatic carbonyl compounds have been previously reported, see:, in: Handbook of Organopalladium Chemistry for Organic Synthesis (Eds.:, Wiley-Interscience, New York, I, chapter IV.2.1.1, p. 1145-1146. The formation of β-aromatic α,β-unsaturated alcohols in the Heck reactions of aryl halides with allylic alcohols has been achieved by the use of a silver salt (silver acetate as the base), see
- Palladium-catalyzed reactions of aromatic halides with allylic alcohols leading to the formation of β-aromatic carbonyl compounds have been previously reported, see:, M. Larhed, A. Hallberg, Scope, Mechanism, and Other Fundamental Aspects of the Intermolecular Heck Reaction, in: Handbook of Organopalladium Chemistry for Organic Synthesis (Eds.:, E. Negishi, A. de Meijere), Wiley-Interscience, New York, 2002, vol. I, chapter IV.2.1.1, p. 1145-1146. The formation of β-aromatic α,β-unsaturated alcohols in the Heck reactions of aryl halides with allylic alcohols has been achieved by the use of a silver salt (silver acetate as the base), see
- (2002) Scope, Mechanism, and Other Fundamental Aspects of the Intermolecular Heck Reaction
- Larhed, M.¹ Hallberg, A.² Negishi, E.³ De Meijere, A.⁴

71
- 0025892690
- T. Jeffery, Tetrahedron Lett. 1991, 32, 2121-2124.
- (1991) Tetrahedron Lett. , vol.32 , pp. 2121-2124
- Jeffery, T.¹

72
- 84962376102
- M. García-Melchor, M. C. Pacheco, C. Nájera, A. Lledõs, G. Ujaque, ACS Catal. 2012, 2, 135-144.
- (2012) ACS Catal. , vol.2 , pp. 135-144
- García-Melchor, M.¹ Pacheco, M.C.² Nájera, C.³ Lledõs, A.⁴ Ujaque, G.⁵

73
- 33845183480
- Y. Hanataka, T. Hiyama, J. Org. Chem. 1989, 54, 268-270.
- (1989) J. Org. Chem. , vol.54 , pp. 268-270
- Hanataka, Y.¹ Hiyama, T.²

74
- 0031023975
- E. Hagiwara, K. Gouda, Y. Hatanaka, T. Hiyama, Tetrahedron Lett. 1997, 38, 439-442.
- (1997) Tetrahedron Lett. , vol.38 , pp. 439-442
- Hagiwara, E.¹ Gouda, K.² Hatanaka, Y.³ Hiyama, T.⁴

75
- 55949115630
- X. Zhang, A. Liu, W. Chen, Org. Lett. 2008, 10, 3849-3852.
- (2008) Org. Lett. , vol.10 , pp. 3849-3852
- Zhang, X.¹ Liu, A.² Chen, W.³

76
- 84861553443
- P. Colbon, J. H. Barnard, M. Purdie, K. Mulholland, I. Kozhevnikov, J. Xiao, Adv. Synth. Catal. 2012, 354, 1395-1400.
- (2012) Adv. Synth. Catal. , vol.354 , pp. 1395-1400
- Colbon, P.¹ Barnard, J.H.² Purdie, M.³ Mulholland, K.⁴ Kozhevnikov, I.⁵ Xiao, J.⁶

77
- 78649770717
- S. Wu, H. Ma, X. Jia, Y. Zhong, Z. Lei, Tetrahedron 2011, 67, 250-256.
- (2011) Tetrahedron , vol.67 , pp. 250-256
- Wu, S.¹ Ma, H.² Jia, X.³ Zhong, Y.⁴ Lei, Z.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.