SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Volumn 70, Issue 9, 2014, Pages 1818-1826

Solvent-free Brønsted acid catalysed alkylation of arenes and heteroarenes with benzylic alcohols

(6) Barbero, Margherita a Cadamuro, Silvano a Dughera, Stefano a Rucci, Marta a Spano, Giulia a Venturello, Paolo a

a UNIVERSITY OF TURIN (Italy)

Author keywords

Benzylic alcohols; Br nsted acid catalyst; Nucleophilicity; Triarylmethanes

Indexed keywords

BENZYL ALCOHOL; BRONSTED ACID; HETEROARENE; METHANE; POLYCYCLIC AROMATIC HYDROCARBON; SOLVENT; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CATALYSIS; ELECTROPHILICITY; NUCLEOPHILICITY; PRIORITY JOURNAL;

EID: 84893752188 PISSN: 00404020 EISSN: 14645416 Source Type: Journal
DOI: 10.1016/j.tet.2014.01.011 Document Type: Article

Times cited : (21)

References (47)

1
- 84872736929
- R. Kumar, and E.V. Van der Eycken Chem. Soc. Rev. 42 2013 1121 1146
- (2013) Chem. Soc. Rev. , vol.42 , pp. 1121-1146
- Kumar, R.¹ Van Der Eycken, E.V.²

2
- 64149095592
- M. Bandini, and M. Tragni Org. Biomol. Chem. 7 2009 1501 1507
- (2009) Org. Biomol. Chem. , vol.7 , pp. 1501-1507
- Bandini, M.¹ Tragni, M.²

3
- 79251622073
- E. Emer, R. Sinisi, M. Guiteras Capdevila, D. Petruziello, F. De Vincentiis, and P.G. Cozzi Eur. J. Org. Chem. 2011 647 666
- (2011) Eur. J. Org. Chem. , pp. 647-666
- Emer, E.¹ Sinisi, R.² Guiteras Capdevila, M.³ Petruziello, D.⁴ De Vincentiis, F.⁵ Cozzi, P.G.⁶

4
- 84872088501
- A. Gualandi, and P.G. Cozzi Synlett 2013 281 296
- (2013) Synlett , pp. 281-296
- Gualandi, A.¹ Cozzi, P.G.²

5
- 77649165966
- M. Rueping, and B.J. Nachtsheim Beilstein J. Org. Chem. 6 2010 6
- (2010) Beilstein J. Org. Chem. , vol.6 , pp. 6
- Rueping, M.¹ Nachtsheim, B.J.²

6
- 77949567825
- P. Thirupathi, and S.S. Kim Tetrahedron 66 2010 2995 3003
- (2010) Tetrahedron , vol.66 , pp. 2995-3003
- Thirupathi, P.¹ Kim, S.S.²

7
- 35348993725
- J.S. Yadav, D.C. Bhunia, K. Vamshi Krishna, and P. Srihari Tetrahedron Lett. 48 2007 8306 8310
- (2007) Tetrahedron Lett. , vol.48 , pp. 8306-8310
- Yadav, J.S.¹ Bhunia, D.C.² Vamshi Krishna, K.³ Srihari, P.⁴

8
- 34548379937
- U. Jana, S. Maiti, and S. Biswas Tetrahedron Lett. 48 2007 7160 7163
- (2007) Tetrahedron Lett. , vol.48 , pp. 7160-7163
- Jana, U.¹ Maiti, S.² Biswas, S.³

9
- 34547482995
- Y.S. Yadav, B.V. Subba Reddy, S. Aravind, G.G.K.S. Narayana Kumar, and A. Srinivas Reddy Tetrahedron Lett. 48 2007 6117 6120
- (2007) Tetrahedron Lett. , vol.48 , pp. 6117-6120
- Yadav, Y.S.¹ Subba Reddy, B.V.² Aravind, S.³ Narayana Kumar, G.G.K.S.⁴ Srinivas Reddy, A.⁵

10
- 31444456960
- M. Yasuda, T. Somyo, and A. Baba Angew. Chem., Int. Ed. 45 2006 793 796
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 793-796
- Yasuda, M.¹ Somyo, T.² Baba, A.³

11
- 0345686459
- M. Noji, T. Ohno, K. Fuji, N. Futaba, H. Tajima, and K. Ishii J. Org. Chem. 68 2003 9340 9347
- (2003) J. Org. Chem. , vol.68 , pp. 9340-9347
- Noji, M.¹ Ohno, T.² Fuji, K.³ Futaba, N.⁴ Tajima, H.⁵ Ishii, K.⁶

12
- 84877897117
- M. Wilsdorf, D. Leichnitz, and H.-U. Reissig Org. Lett. 15 2013 2494 2497
- (2013) Org. Lett. , vol.15 , pp. 2494-2497
- Wilsdorf, M.¹ Leichnitz, D.² Reissig, H.-U.³

13
- 33745632148
- V.D. Sarca, and K.K. Laali Green Chem. 8 2006 615 620
- (2006) Green Chem. , vol.8 , pp. 615-620
- Sarca, V.D.¹ Laali, K.K.²

14
- 79955641928
- J. Gao, J.-Q. Wang, Q.-W. Song, and L.-N. He Green Chem. 13 2011 1182 1186
- (2011) Green Chem. , vol.13 , pp. 1182-1186
- Gao, J.¹ Wang, J.-Q.² Song, Q.-W.³ He, L.-N.⁴

15
- 79955578042
- A. Zhou, L. Li, J. Wang, and K. Zhuo Green Chem. 13 2011 1244 1250
- (2011) Green Chem. , vol.13 , pp. 1244-1250
- Zhou, A.¹ Li, L.² Wang, J.³ Zhuo, K.⁴

16
- 34347324087
- J. Le Bras, and J. Muzart Tetrahedron 63 2007 7942 7948
- (2007) Tetrahedron , vol.63 , pp. 7942-7948
- Le Bras, J.¹ Muzart, J.²

17
- 33749315860
- R. Sanz, A. Martinez, D. Miguel, J.M. Alvarez-Gutierrez, and F. Rodrigues Adv. Synth. Catal. 348 2006 1841 1845
- (2006) Adv. Synth. Catal. , vol.348 , pp. 1841-1845
- Sanz, R.¹ Martinez, A.² Miguel, D.³ Alvarez-Gutierrez, J.M.⁴ Rodrigues, F.⁵

18
- 84863855617
- Y. Sato, T. Aoyama, T. Takido, and M. Kodomari Tetrahedron 68 2012 7077 7081
- (2012) Tetrahedron , vol.68 , pp. 7077-7081
- Sato, Y.¹ Aoyama, T.² Takido, T.³ Kodomari, M.⁴

19
- 38349038186
- J.S. Yadav, B.V. Subba Reddy, and A. Srinivas Reddy J. Mol. Catal. A Chem. 280 2008 219 223
- (2008) J. Mol. Catal. A Chem. , vol.280 , pp. 219-223
- Yadav, J.S.¹ Subba Reddy, B.V.² Srinivas Reddy, A.³

20
- 34547613570
- K. Motokura, N. Nakagiri, T. Mizugaki, K. Ebitani, and K. Kaneda J. Org. Chem. 72 2007 6006 6015
- (2007) J. Org. Chem. , vol.72 , pp. 6006-6015
- Motokura, K.¹ Nakagiri, N.² Mizugaki, T.³ Ebitani, K.⁴ Kaneda, K.⁵

21
- 33846580543
- S. Shirikawa, and S. Kobayashi Org. Lett. 9 2007 311 314
- (2007) Org. Lett. , vol.9 , pp. 311-314
- Shirikawa, S.¹ Kobayashi, S.²

22
- 53549118306
- P.G. Cozzi, and L. Zoli Angew. Chem., Int. Ed. 47 2008 4162 4166
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4162-4166
- Cozzi, P.G.¹ Zoli, L.²

23
- 77449161619
- T. Hirashita, S. Kuwahara, S. Okochi, M. Tsuji, and S. Araki Tetrahedron Lett. 51 2010 1847 1851
- (2010) Tetrahedron Lett. , vol.51 , pp. 1847-1851
- Hirashita, T.¹ Kuwahara, S.² Okochi, S.³ Tsuji, M.⁴ Araki, S.⁵

24
- 80051581769
- B. Zhou, J. Yang, M. Li, and Y. Gu Green Chem. 13 2011 2204 2211
- (2011) Green Chem. , vol.13 , pp. 2204-2211
- Zhou, B.¹ Yang, J.² Li, M.³ Gu, Y.⁴

25
- 77949987753
- J.A. McCubbin, and O.V. Kronin Tetrahedron Lett. 51 2010 2447 2449
- (2010) Tetrahedron Lett. , vol.51 , pp. 2447-2449
- McCubbin, J.A.¹ Kronin, O.V.²

26
- 84860645078
- M. Barbero, S. Cadamuro, F. Cauda, S. Dughera, G. Gervasio, and P. Venturello J. Org. Chem. 77 2012 4278 4287
- (2012) J. Org. Chem. , vol.77 , pp. 4278-4287
- Barbero, M.¹ Cadamuro, S.² Cauda, F.³ Dughera, S.⁴ Gervasio, G.⁵ Venturello, P.⁶

27
- 0031850093
- M. Barbero, M. Crisma, I. Degani, R. Fochi, and P. Perracino Synthesis 1998 1171 1175
- (1998) Synthesis , pp. 1171-1175
- Barbero, M.¹ Crisma, M.² Degani, I.³ Fochi, R.⁴ Perracino, P.⁵

28
- 84857617451
- For use of this Brønsted acid as catalyst in organic syntheses, see:, and references therein
- For use of this Brønsted acid as catalyst in organic syntheses, see: M. Barbero, S. Cadamuro, S. Dughera, C. Magistris, and P. Venturello Org. Biomol. Chem. 9 2011 8393 8399 and references therein
- (2011) Org. Biomol. Chem. , vol.9 , pp. 8393-8399
- Barbero, M.¹ Cadamuro, S.² Dughera, S.³ Magistris, C.⁴ Venturello, P.⁵

29
- 0035802329
- H. Mayr, T. Bug, M.F. Gotta, N. Hering, B. Irrgang, B. Janker, B. Kempf, R. Loos, A.R. Ofial, G. Remennikov, and H. Schimmel J. Am. Chem. Soc. 123 2001 9500 9512
- (2001) J. Am. Chem. Soc. , vol.123 , pp. 9500-9512
- Mayr, H.¹ Bug, T.² Gotta, M.F.³ Hering, N.⁴ Irrgang, B.⁵ Janker, B.⁶ Kempf, B.⁷ Loos, R.⁸ Ofial, A.R.⁹ Remennikov, G.¹⁰ Schimmel, H.¹¹

30
- 0037241494
- H. Mayr, B. Kempf, and A.R. Ofial Acc. Chem. Res. 36 2003 66 77
- (2003) Acc. Chem. Res. , vol.36 , pp. 66-77
- Mayr, H.¹ Kempf, B.² Ofial, A.R.³

31
- 84866281848
- H. Mayr, S. Lakhdar, B. Maji, and A.R. Ofial Beilstein J. Org. Chem. 8 2012 1458 1478
- (2012) Beilstein J. Org. Chem. , vol.8 , pp. 1458-1478
- Mayr, H.¹ Lakhdar, S.² Maji, B.³ Ofial, A.R.⁴

32
- 84893767946
- For a comprehensive database of electrophilicity parameters E and nucleophilicity parameters N and s, see http://www.Cup.uni-muenchen.de/oc/mayr/ DBintro.html.

33
- 0035966625
- P.E. Gordon, and A.J. Fry Tetrahedron Lett. 42 2001 831 833
- (2001) Tetrahedron Lett. , vol.42 , pp. 831-833
- Gordon, P.E.¹ Fry, A.J.²

34
- 0006298213
- G.J. Esselen, and L. Clarke J. Am. Chem. Soc. 36 1914 308 324
- (1914) J. Am. Chem. Soc. , vol.36 , pp. 308-324
- Esselen, G.J.¹ Clarke, L.²

35
- 26844433958
- B. Pal, V. Sesha Giri, and P. Jaisankar Catal. Commun. 6 2005 711 715
- (2005) Catal. Commun. , vol.6 , pp. 711-715
- Pal, B.¹ Sesha Giri, V.² Jaisankar, P.³

36
- 37049066995
- H. Ishii J. Chem. Soc., Perkin Trans. 1 1988 2377 2385
- (1988) J. Chem. Soc., Perkin Trans. 1 , pp. 2377-2385
- Ishii, H.¹

37
- 84865793021
- A.M. Costero, M. Parra, S. Gil, R. Gotor, R. Martinez-Manez, F. Sancenon, and S. Royo Eur. J. Org. Chem. 2012 4937 4946
- (2012) Eur. J. Org. Chem. , pp. 4937-4946
- Costero, A.M.¹ Parra, M.² Gil, S.³ Gotor, R.⁴ Martinez-Manez, R.⁵ Sancenon, F.⁶ Royo, S.⁷

38
- 0032567293
- M.F. Gotta, and H. Mayr J. Org. Chem. 63 1998 9769 9775
- (1998) J. Org. Chem. , vol.63 , pp. 9769-9775
- Gotta, M.F.¹ Mayr, H.²

39
- 84876716300
- G. Berionni, V. Morozova, M. Heininger, P. Mayer, P. Knochel, and H. Mayr J. Am. Chem. Soc. 135 2013 6317 6324
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 6317-6324
- Berionni, G.¹ Morozova, V.² Heininger, M.³ Mayer, P.⁴ Knochel, P.⁵ Mayr, H.⁶

40
- 84893812677
- T. Szeki Chem. Ber. 56B 1923 2464 2468
- (1923) Chem. Ber. , vol.56 B , pp. 2464-2468
- Szeki, T.¹

41
- 0028555488
- R. Muthyala, A.R. Katritzky, and X. Lan Dyes Pigm. 25 1994 303 324
- (1994) Dyes Pigm. , vol.25 , pp. 303-324
- Muthyala, R.¹ Katritzky, A.R.² Lan, X.³

42
- 79955030797
- J. Liu, T. He, and L. Wang Tetrahedron 67 2011 3420 3426
- (2011) Tetrahedron , vol.67 , pp. 3420-3426
- Liu, J.¹ He, T.² Wang, L.³

43
- 84878073179
- I. Wu, R. Jiang, J.-M. Yang, S.-Y. Wang, and S.-J. Ji RSC Adv. 3 2013 5459 5464
- (2013) RSC Adv. , vol.3 , pp. 5459-5464
- Wu, I.¹ Jiang, R.² Yang, J.-M.³ Wang, S.-Y.⁴ Ji, S.-J.⁵

44
- 7244238073
- M. Hofmann, N. Hampel, T. Kanzian, and H. Mayr Angew. Chem., Int. Ed. 43 2004 5402 5405
- (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 5402-5405
- Hofmann, M.¹ Hampel, N.² Kanzian, T.³ Mayr, H.⁴

45
- 35648936917
- L.-T. An, F.-Q. Ding, and J.-P. Zou Dyes Pigm. 77 2008 478 480
- (2008) Dyes Pigm. , vol.77 , pp. 478-480
- An, L.-T.¹ Ding, F.-Q.² Zou, J.-P.³

46
- 33745971431
- X. Wang J. Mol. Catal. A Chem. 255 2006 31 35
- (2006) J. Mol. Catal. A Chem. , vol.255 , pp. 31-35
- Wang, X.¹

47
- 48049083975
- S. Aburatani, and J. Uenishi Heterocycles 75 2008 1407 1416
- (2008) Heterocycles , vol.75 , pp. 1407-1416
- Aburatani, S.¹ Uenishi, J.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.