SCOPUS 정보 검색 플랫폼

RSC Advances

Volumn 3, Issue 44, 2013, Pages 21369-21372

Bio-based green solvent mediated disulfide synthesis via thiol couplings free of catalyst and additive

(5) Liu, Yunyun a Wang, Hang a Wang, Chunping a Wan, Jie Ping a Wen, Chengping b

a JIANGXI NORMAL UNIVERSITY (China)

b ZHEJIANG CHINESE MEDICAL UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS;

BIO-BASED; DISULFIDE SYNTHESIS; ETHYL LACTATE; GREEN SOLVENTS; OXIDATIVE COUPLING REACTIONS; PROMOTION EFFECTS;

SOLVENTS;

EID: 84886495336 PISSN: None EISSN: 20462069 Source Type: Journal
DOI: 10.1039/c3ra42915f Document Type: Article

Times cited : (77)

References (41)

1
- 80053515293
- C. S. M. Pereira V. M. T. M. Silva R. E. Rodrigues Green Chem. 2011 13 2658 2671
- (2011) Green Chem. , vol.13 , pp. 2658-2671
- Pereira, C.S.M.¹ Silva, V.M.T.M.² Rodrigues, R.E.³

2
- 58149291586
- S. Aparicio R. Alcalde Green Chem. 2009 11 65 78
- (2009) Green Chem. , vol.11 , pp. 65-78
- Aparicio, S.¹ Alcalde, R.²

3
- 84876938321
- J.-P. Wan C. Wang R. Zhou Y. Liu RSC Adv. 2012 2 8789 8792
- (2012) RSC Adv. , vol.2 , pp. 8789-8792
- Wan, J.-P.¹ Wang, C.² Zhou, R.³ Liu, Y.⁴

4
- 67649419548
- J. S. Bennett K. L. Charles M. R. Miner C. F. Heuberger E. J. Spina M. F. Bartels T. Foreman Green Chem. 2009 11 166 168
- (2009) Green Chem. , vol.11 , pp. 166-168
- Bennett, J.S.¹ Charles, K.L.² Miner, M.R.³ Heuberger, C.F.⁴ Spina, E.J.⁵ Bartels, M.F.⁶ Foreman, T.⁷

5
- 84870402818
- P. P. Ghosh S. Paul A. R. Das Tetrahedron Lett. 2013 54 138 142
- (2013) Tetrahedron Lett. , vol.54 , pp. 138-142
- Ghosh, P.P.¹ Paul, S.² Das, A.R.³

6
- 0004212770
- American Press, NewYork
- P. C. Jocelyn, Biochemistry of the Thiol Group, American Press, NewYork, 1992
- (1992) Biochemistry of the Thiol Group
- Jocelyn, P.C.¹

7
- 0029035467
- B. D. Palmer G. W. Newcastle A. M. Thompson M. Boyd H. D. H. Showalter A. D. Sercel D. W. Fry A. J. Kraker W. A. Dennyyrosine J. Med. Chem. 1995 38 58 67
- (1995) J. Med. Chem. , vol.38 , pp. 58-67
- Palmer, B.D.¹ Newcastle, G.W.² Thompson, A.M.³ Boyd, M.⁴ Showalter, H.D.H.⁵ Sercel, A.D.⁶ Fry, D.W.⁷ Kraker, A.J.⁸ Dennyyrosine, W.A.⁹

8
- 84886537853
- Y. Kanda T. Fukuyama J. Am. Chem. Soc. 1993 115 84451 84452
- (1993) J. Am. Chem. Soc. , vol.115 , pp. 84451-84452
- Kanda, Y.¹ Fukuyama, T.²

9
- 84867931154
- L.-H. Zou J. Reball J. Mottweiler C. Bolm Chem. Commun. 2012 11307 11309
- (2012) Chem. Commun. , pp. 11307-11309
- Zou, L.-H.¹ Reball, J.² Mottweiler, J.³ Bolm, C.⁴

10
- 84859727783
- G. L. Regina V. Gatti V. Famiglini F. Piscitelli R. Silvestri ACS Comb. Sci. 2012 14 258 262
- (2012) ACS Comb. Sci. , vol.14 , pp. 258-262
- Regina, G.L.¹ Gatti, V.² Famiglini, V.³ Piscitelli, F.⁴ Silvestri, R.⁵

11
- 70350078396
- K. R. Prabhu P. S. Sivanand S. Chandrasekaran Angew. Chem., Int. Ed. 2000 39 4136 4139
- (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 4136-4139
- Prabhu, K.R.¹ Sivanand, P.S.² Chandrasekaran, S.³

12
- 70350724455
- I. Popov H.-Q. Do O. Daugulis J. Org. Chem. 2009 74 8309 8313
- (2009) J. Org. Chem. , vol.74 , pp. 8309-8313
- Popov, I.¹ Do, H.-Q.² Daugulis, O.³

13
- 34548691450
- H. Shirani T. Janosik Synthesis 2007 2690 2698
- (2007) Synthesis , pp. 2690-2698
- Shirani, H.¹ Janosik, T.²

14
- 42049083143
- N. Taniguchi Synlett 2008 849 852
- (2008) Synlett , pp. 849-852
- Taniguchi, N.¹

15
- 0030767201
- J. B. Arterburm M. C. Perry S. L. Nelson B. R. Dible M. S. Holguin J. Am. Chem. Soc. 1997 119 9309 9310
- (1997) J. Am. Chem. Soc. , vol.119 , pp. 9309-9310
- Arterburm, J.B.¹ Perry, M.C.² Nelson, S.L.³ Dible, B.R.⁴ Holguin, M.S.⁵

16
- 0000204549
- J. Choi N. M. Yoon J. Org. Chem. 1995 60 3266 3267
- (1995) J. Org. Chem. , vol.60 , pp. 3266-3267
- Choi, J.¹ Yoon, N.M.²

17
- 84871665199
- A. Dhakshinamoorthy S. Navalon D. Sempere M. Alvaro H. Garcia ChemCatChem 2013 5 241 246
- (2013) ChemCatChem , vol.5 , pp. 241-246
- Dhakshinamoorthy, A.¹ Navalon, S.² Sempere, D.³ Alvaro, M.⁴ Garcia, H.⁵

18
- 33947725293
- A. Saxena A. Kumar S. Mozumdar J. Mol. Catal. A: Chem. 2007 269 35 40
- (2007) J. Mol. Catal. A: Chem. , vol.269 , pp. 35-40
- Saxena, A.¹ Kumar, A.² Mozumdar, S.³

19
- 0001224436
- A. R. Ramesha S. Chandrasekran J. Org. Chem. 1994 59 1354 1357
- (1994) J. Org. Chem. , vol.59 , pp. 1354-1357
- Ramesha, A.R.¹ Chandrasekran, S.²

20
- 1242271367
- M. Tajbakhsh R. Hosseinzadeh A. Sharoori Tetrahedron Lett. 2004 45 1889 1893
- (2004) Tetrahedron Lett. , vol.45 , pp. 1889-1893
- Tajbakhsh, M.¹ Hosseinzadeh, R.² Sharoori, A.³

21
- 14944350357
- A. Shaabani F. Tavasoli-Rad D. G. Lee Synth. Commun. 2005 35 571 580
- (2005) Synth. Commun. , vol.35 , pp. 571-580
- Shaabani, A.¹ Tavasoli-Rad, F.² Lee, D.G.³

22
- 0028865019
- K. Ramadas N. Srinivasan Synth. Commun. 1995 25 227 234
- (1995) Synth. Commun. , vol.25 , pp. 227-234
- Ramadas, K.¹ Srinivasan, N.²

23
- 0000806851
- D. L. De Leeuw W. K. Musker J. T. Doi J. Org. Chem. 1982 47 4860 4864
- (1982) J. Org. Chem. , vol.47 , pp. 4860-4864
- De Leeuw, D.L.¹ Musker, W.K.² Doi, J.T.³

24
- 0005693463
- W. A. Pryor D. F. Church C. K. Govindan G. Grank J. Org. Chem. 1982 47 156 159
- (1982) J. Org. Chem. , vol.47 , pp. 156-159
- Pryor, W.A.¹ Church, D.F.² Govindan, C.K.³ Grank, G.⁴

25
- 0034006677
- V. Kesavan D. Bonnet-Dulpon J.-P. Bégué Synthesis 2000 223 225
- (2000) Synthesis , pp. 223-225
- Kesavan, V.¹ Bonnet-Dulpon, D.² Bégué, J.-P.³

26
- 79956149677
- M. Oba K. Tanaka K. Nishiyama W. Ando J. Org. Chem. 2011 76 4173 4177
- (2011) J. Org. Chem. , vol.76 , pp. 4173-4177
- Oba, M.¹ Tanaka, K.² Nishiyama, K.³ Ando, W.⁴

27
- 0030793274
- M. Hirano S. Yakabe M. Fukami T. Morimoto Synth. Commun. 1997 27 2783 2788
- (1997) Synth. Commun. , vol.27 , pp. 2783-2788
- Hirano, M.¹ Yakabe, S.² Fukami, M.³ Morimoto, T.⁴

28
- 44649151664
- J. L. G. Ruano A. Parra J. Alemán Green Chem. 2008 10 706 711
- (2008) Green Chem. , vol.10 , pp. 706-711
- Ruano, J.L.G.¹ Parra, A.² Alemán, J.³

29
- 33751174494
- A. Christoforou G. Nicolaou Y. Elemes Tetrahedron Lett. 2006 47 9211
- (2006) Tetrahedron Lett. , vol.47 , pp. 9211
- Christoforou, A.¹ Nicolaou, G.² Elemes, Y.³

30
- 78651110462
- S. Thurow V. A. Pereira D. M. Martinez D. Alves G. Perin R. G. Jacob E. J. Lenardão Tetrahedron Lett. 2011 52 640 643
- (2011) Tetrahedron Lett. , vol.52 , pp. 640-643
- Thurow, S.¹ Pereira, V.A.² Martinez, D.M.³ Alves, D.⁴ Perin, G.⁵ Jacob, R.G.⁶ Lenardão, E.J.⁷

31
- 80053974929
- D. R. Dreyer H.-P. Jia A. D. Todd J. Geng C. W. Bielawski Org. Biomol. Chem. 2011 9 7292 7295
- (2011) Org. Biomol. Chem. , vol.9 , pp. 7292-7295
- Dreyer, D.R.¹ Jia, H.-P.² Todd, A.D.³ Geng, J.⁴ Bielawski, C.W.⁵

32
- 0032907261
- N. Iranpoor B. Zeynizadeh Synthesis 1999 49 50
- (1999) Synthesis , pp. 49-50
- Iranpoor, N.¹ Zeynizadeh, B.²

33
- 78651235946
- L. Menini M. C. Pereira A. C. Ferreira J. D. Fabris E. V. Gusevskaya Appl. Catal., A 2011 392 151 157
- (2011) Appl. Catal., A , vol.392 , pp. 151-157
- Menini, L.¹ Pereira, M.C.² Ferreira, A.C.³ Fabris, J.D.⁴ Gusevskaya, E.V.⁵

34
- 0141608196
- S. M. S. Chauhan A. Kumar K. A. Srinivas Chem. Commun. 2003 2348 2349
- (2003) Chem. Commun. , pp. 2348-2349
- Chauhan, S.M.S.¹ Kumar, A.² Srinivas, K.A.³

35
- 79961078081
- A. Ghorbani-Choghamarani M. Nikoorazm H. Goudarziafshar A. Shokr H. Almasi J. Chem. Sci. 2011 123 453 457
- (2011) J. Chem. Sci. , vol.123 , pp. 453-457
- Ghorbani-Choghamarani, A.¹ Nikoorazm, M.² Goudarziafshar, H.³ Shokr, A.⁴ Almasi, H.⁵

36
- 79551602248
- A. Ghorbani-Choghamarani S. Sardari J. Sulfur Chem. 2011 32 63 69
- (2011) J. Sulfur Chem. , vol.32 , pp. 63-69
- Ghorbani-Choghamarani, A.¹ Sardari, S.²

37
- 84879486275
- During the submission of our manuscript, U. Beifuss and B. C. Ranu reported laccase-catalyzed and Al3O2 assisted ball milling synthesis of disulfides using thiols oxidation, respectively, see
- Z. Li F. Ke H. Deng H. Xu H. Xiang X. Zhou Org. Biomol. Chem. 2013 11 2943 2946
- (2013) Org. Biomol. Chem. , vol.11 , pp. 2943-2946
- Li, Z.¹ Ke, F.² Deng, H.³ Xu, H.⁴ Xiang, H.⁵ Zhou, X.⁶

38
- 84882384594
- H. T. Abdel-Mohsen K. Sudheendran J. Conrad U. Beifuss Green Chem. 2013 15 1490 1495
- (2013) Green Chem. , vol.15 , pp. 1490-1495
- Abdel-Mohsen, H.T.¹ Sudheendran, K.² Conrad, J.³ Beifuss, U.⁴

39
- 84881427262
- For other green procedures on disulfide synthesis, see
- T. Chatterjee B. C. Ranu RSC Adv. 2013 3 10680 10686
- (2013) RSC Adv. , vol.3 , pp. 10680-10686
- Chatterjee, T.¹ Ranu, B.C.²

40
- 2642616994
- M. Sridhar S. K. Vadivel U. T. Bhalerao Synth. Commun. 1998 28 1499 1502
- (1998) Synth. Commun. , vol.28 , pp. 1499-1502
- Sridhar, M.¹ Vadivel, S.K.² Bhalerao, U.T.³

41
- 84863262061
- We thank our referee for suggesting the control experiments as this helped us to obtain more accurate clues on the reaction mechanism
- P. Attri S. Gupta R. Kumar Green Chem. Lett. Rev. 2012 5 33 42
- (2012) Green Chem. Lett. Rev. , vol.5 , pp. 33-42
- Attri, P.¹ Gupta, S.² Kumar, R.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.