SCOPUS 정보 검색 플랫폼

Volumn 90, Issue 5, 2012, Pages 464-468

Highly efficient solvent-free acetylation of alcohols with acetic anhydride catalyzed by recyclable sulfonic acid catalyst (SBA-15-Ph-Pr-SO 3H)- An environmentally benign method

(3) Zareyee, Daryoush a Ghadikolaee, Abdollah Razaghi a Khalilzadeh, Mohammad A a

a ISLAMIC AZAD UNIVERSITY (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ANHYDRIDES; ENVIRONMENTALLY BENIGN; ENVIRONMENTALLY BENIGN REACTION; EXPERIMENTAL PROCEDURE; FUNCTIONALIZED; NANO-STRUCTURED; REACTION CYCLES; SALIENT FEATURES; SOLVENT FREE; SOLVENT FREE CONDITIONS; SULFONIC ACID;

ACETYLATION; PH EFFECTS; PHENOLS; REUSABILITY;

SOLVENTS;

EID: 84860516300 PISSN: 00084042 EISSN: None Source Type: Journal
DOI: 10.1139/v2012-018 Document Type: Article

Times cited : (13)

References (26)

1
- 84860510837
- Green, T. W. Wuts, P. G. M. Protective Groups in Organic Synthesis; 3rd ed. John Wiley & Sons: New York, 1999; p 150.
- Green, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis; 3rd ed.; John Wiley & Sons: New York, 1999; p 150.

2
- 84860538898
- Hanson, J. R. Protective Groups in Organic Synthesis; Blackwell Science: Malden, MA, 1999.
- Hanson, J. R. Protective Groups in Organic Synthesis; Blackwell Science: Malden, MA, 1999.

3
- 84988138413
- 10.1055/s-1975-23714
- Zhdanov R. I. Zhenodarova S. M. Synthesis 1975, 1975 (4), 222. 10.1055/s-1975-23714
- (1975) Synthesis , vol.1975 , Issue.4 , pp. 222
- Zhdanov, R.I.¹ Zhenodarova, S.M.²

4
- 26444581289
- Tomohumi S. Kousaburo O. Takeshi O. Synthesis 1999, 1141.
- (1999) Synthesis , pp. 1141
- Tomohumi, S.¹ Kousaburo, O.² Takeshi, O.³

5
- 0017998510
- 10.1002/anie.197805691
- Höfle G. Steglich V. Vorbraggen H. Angew. Chem. Int. Ed. Engl. 1978, 17 (8), 569. 10.1002/anie.197805691
- (1978) Angew. Chem. Int. Ed. Engl. , vol.17 , Issue.8 , pp. 569
- Höfle, G.¹ Steglich, V.² Vorbraggen, H.³

6
- 0000991014
- Wiley: New York
- Cope, A. C.; Herrick, E. C. In Organic Syntheses Collective; Wiley: New York, 1963; Vol. IV, p 304.
- (1963) Organic Syntheses Collective , vol.4 , pp. 304
- Cope, A.C.¹ Herrick, E.C.²

7
- 0012615648
- 10.1021/jo952237x
- Ishihara K. Kubota M. Kurihara H. Yamamoto H. J. Org. Chem. 1996, 61 (14), 4560. 10.1021/jo952237x
- (1996) J. Org. Chem. , vol.61 , Issue.14 , pp. 4560
- Ishihara, K.¹ Kubota, M.² Kurihara, H.³ Yamamoto, H.⁴

8
- 0032753189
- 10.1055/s-1999-2941
- Chauhan K. K. Frost C. G. Love I. Waite D. Synlett 1999, 1999 (11), 1743. 10.1055/s-1999-2941
- (1999) Synlett , vol.1999 , Issue.11 , pp. 1743
- Chauhan, K.K.¹ Frost, C.G.² Love, I.³ Waite, D.⁴

9
- 0037492241
- Highly efficient and versatile acetylation of alcohols catalyzed by cerium(III) triflate
- DOI 10.1016/S0040-4039(03)01358-3
- Dalpozzo R. De Nino A. Maiuolo L. Procopio A. Nardi M. Bartoli G. Romeo R. Tetrahedron Lett. 2003, 44 (30), 5621. 10.1016/S0040-4039(03)01358-3 (Pubitemid 36782593)
- (2003) Tetrahedron Letters , vol.44 , Issue.30 , pp. 5621-5624
- Dalpozzo, R.¹ De Nino, A.² Maiuolo, L.³ Procopio, A.⁴ Nardi, M.⁵ Bartoli, G.⁶ Romeo, R.⁷

10
- 11144256407
- 10.1016/j.molcata.2004.09.024
- Alleti R. Perambuduru M. Samantha S. Reddy V. P. J. Mol. Catal. A Chem. 2005, 226 (1), 57. 10.1016/j.molcata.2004.09.024
- (2005) J. Mol. Catal. A Chem. , vol.226 , Issue.1 , pp. 57
- Alleti, R.¹ Perambuduru, M.² Samantha, S.³ Reddy, V.P.⁴

11
- 34247582284
- 3 as a highly efficient catalyst for the rapid acetylation of alcohols, phenols and thiophenols under solvent-free conditions
- DOI 10.1016/j.tetlet.2007.03.162, PII S0040403907006387
- Kamal A. Khan M. N. A. Reddy K. S. Srikanth Y. V. V. Krishnaji T. Tetrahedron Lett. 2007, 48 (22), 3813. 10.1016/j.tetlet.2007.03.162 (Pubitemid 46669668)
- (2007) Tetrahedron Letters , vol.48 , Issue.22 , pp. 3813-3818
- Kamal, A.¹ Khan, M.N.A.² Reddy, K.S.³ Srikanth, Y.V.V.⁴ Krishnaji, T.⁵

12
- 33244463561
- Catalytic acetylation of alcohols and phenols with ferric perchlorate in acetic acid
- DOI 10.1016/j.catcom.2005.09.011, PII S1566736705002219
- Heravi M. M. Behbahani F. K. Hekmat Shoar R. Oskooie H. A. Catal. Commun. 2006, 7 (3), 136. 10.1016/j.catcom.2005.09.011 (Pubitemid 43276289)
- (2006) Catalysis Communications , vol.7 , Issue.3 , pp. 136-139
- Heravi, M.M.¹ Behbahani, F.K.² Hekmat Shoar, R.³ Oskooie, H.A.⁴

13
- 2542460172
- 10.1016/j.molcata.2004.03.006
- Gowda S. Lokanatha Rai K. M. J. Mol. Catal. Chem. 2004, 217 (1-2), 27. 10.1016/j.molcata.2004.03.006
- (2004) J. Mol. Catal. Chem. , vol.217 , Issue.12 , pp. 27
- Gowda, S.¹ Lokanatha Rai, K.M.²

14
- 2442701279
- Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions
- DOI 10.1016/j.tetlet.2004.04.076, PII S0040403904008664
- Phukan P. Tetrahedron Lett. 2004, 45 (24), 4785. 10.1016/j.tetlet.2004. 04.076 (Pubitemid 38670313)
- (2004) Tetrahedron Letters , vol.45 , Issue.24 , pp. 4785-4787
- Phukan, P.¹

15
- 33747163923
- 2O as a catalyst under solvent-free conditions
- DOI 10.1016/j.tetlet.2006.07.059, PII S0040403906014584
- Reddy T. S. Narasimhulu M. Suryakiran N. Mahesh K. C. Ashalatha K. Venkateswarlu Y. Tetrahedron Lett. 2006, 47 (38), 6825. 10.1016/j.tetlet.2006. 07.059 (Pubitemid 44232896)
- (2006) Tetrahedron Letters , vol.47 , Issue.38 , pp. 6825-6829
- Reddy, T.S.¹ Narasimhulu, M.² Suryakiran, N.³ Mahesh, K.C.⁴ Ashalatha, K.⁵ Venkateswarlu, Y.⁶

16
- 34547411384
- 2
- DOI 10.1016/j.molcata.2007.05.012, PII S1381116907003408
- Moghadam M. Tangestaninejad S. Mirkhani V. Mohammadpoor-Baltork I. Taghavi S. A. J. Mol. Catal. A Chem. 2007, 274 (1-2), 217. 10.1016/j.molcata. 2007.05.012 (Pubitemid 47176465)
- (2007) Journal of Molecular Catalysis A: Chemical , vol.274 , Issue.1-2 , pp. 217-223
- Moghadam, M.¹ Tangestaninejad, S.² Mirkhani, V.³ Mohammadpoor-Baltork, I.⁴ Taghavi, S.A.⁵

17
- 45449106974
- Firouzabadi M. Iranpoor N. Farahi S. J. Mol. Catal. A Chem. 2008, 289, 61.
- (2008) J. Mol. Catal. A Chem. , vol.289 , pp. 61
- Firouzabadi, M.¹ Iranpoor, N.² Farahi, S.³

18
- 77953696206
- 10.1016/j.cej.2009.12.029
- Romanelli G. Ruiz D. Vázquez P. Thomas H. Autino J. C. Chem. Eng. J. 2010, 161 (3), 355. 10.1016/j.cej.2009.12.029
- (2010) Chem. Eng. J. , vol.161 , Issue.3 , pp. 355
- Romanelli, G.¹ Ruiz, D.² Vázquez, P.³ Thomas, H.⁴ Autino, J.C.⁵

19
- 71449101454
- 10.1016/j.molcata.2009.09.021
- Osiglio L. Romanelli G. Blanco M. J. Mol. Catal. A Chem. 2010, 316 (1-2), 52. 10.1016/j.molcata.2009.09.021
- (2010) J. Mol. Catal. A Chem. , vol.316 , Issue.12 , pp. 52
- Osiglio, L.¹ Romanelli, G.² Blanco, M.³

20
- 33947311361
- 3 as a highly efficient and recyclable heterogeneous catalyst for the chemoselective acetylation of alcohols, phenols amines and thiols with acetic anhydride under solvent free conditions
- DOI 10.1016/j.molcata.2006.11.026, PII S1381116906013847
- Joseph J. K. Jain S. L. Sain B. J. Mol. Catal. A Chem. 2007, 267 (1-2), 108. 10.1016/j.molcata.2006.11.026 (Pubitemid 46441935)
- (2007) Journal of Molecular Catalysis A: Chemical , vol.267 , Issue.1-2 , pp. 108-111
- Joseph, J.K.¹ Jain, S.L.² Sain, B.³

21
- 33947723807
- 2 as a heterogeneous catalyst
- DOI 10.1016/j.molcata.2006.12.029, PII S1381116906014531
- Das B. Thirupathi P. J. Mol. Catal. A Chem. 2007, 269 (1-2), 12. 10.1016/j.molcata.2006.12.029 (Pubitemid 46507859)
- (2007) Journal of Molecular Catalysis A: Chemical , vol.269 , Issue.1-2 , pp. 12-16
- Das, B.¹ Thirupathi, P.²

22
- 41649090535
- 10.1016/j.tetlet.2008.03.005
- Yoon H. J. Lee S. M. Kim J. H. Cho H. J. Choi J. W. Lee S. H. Lee Y. S. Tetrahedron Lett. 2008, 49 (19), 3165. 10.1016/j.tetlet.2008.03.005
- (2008) Tetrahedron Lett. , vol.49 , Issue.19 , pp. 3165
- Yoon, H.J.¹ Lee, S.M.² Kim, J.H.³ Cho, H.J.⁴ Choi, J.W.⁵ Lee, S.H.⁶ Lee, Y.S.⁷

23
- 57149121902
- 10.1016/j.tetlet.2008.11.024
- Rajabi F. Tetrahedron Lett. 2009, 50 (4), 395. 10.1016/j.tetlet.2008.11. 024
- (2009) Tetrahedron Lett. , vol.50 , Issue.4 , pp. 395
- Rajabi, F.¹

24
- 68349152408
- 10.1016/j.apcata.2009.07.014
- Niknam K. Saberi D. Appl. Catal. A Gen. 2009, 366 (1), 220. 10.1016/j.apcata.2009.07.014
- (2009) Appl. Catal. A Gen. , vol.366 , Issue.1 , pp. 220
- Niknam, K.¹ Saberi, D.²

25
- 55949099026
- 10.1021/ol8013107 18702496
- Karimi B. Zareyee D. Org. Lett. 2008, 10 (18), 3989. 10.1021/ol8013107 18702496
- (2008) Org. Lett. , vol.10 , Issue.18 , pp. 3989
- Karimi, B.¹ Zareyee, D.²

26
- 72849123170
- 10.1039/b911388f
- Karimi B. Zareyee D. J. Mater. Chem. 2009, 19 (45), 8665. 10.1039/b911388f
- (2009) J. Mater. Chem. , vol.19 , Issue.45 , pp. 8665
- Karimi, B.¹ Zareyee, D.²

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