Lithium Trifluoromethanesulfonate (LiOTf) as a Recyclable Catalyst for Highly Efficient Acetylation of Alcohols and Diacetylation of Aldehydes under Mild and Neutral Reaction Conditions

Babak Karimi; Jafar Maleki

doi:10.1021/jo026678+

journal article May 09, 2003

Lithium Trifluoromethanesulfonate (LiOTf) as a Recyclable Catalyst for Highly Efficient Acetylation of Alcohols and Diacetylation of Aldehydes under Mild and Neutral Reaction Conditions

Babak Karimi Jafar Maleki

The Journal of Organic Chemistry Vol. 68 No. 12 pp. 4951-4954 · American Chemical Society (ACS)

View at Publisher Save 10.1021/jo026678+

Topics

No keywords indexed for this article. Browse by subject →

References

63

[1]

Greene T. W. (1999) 10.1002/0471220574

[2]

(b) Kocienski, P. J.ProtectingGroups; Thieme, New York, 1994.

[3]

(a) Larock, R. C.Comprehensive Organic Transformations; VCH Publishers, Inc. New York, 1989; p 980. For more recent leading references, see: (b) Saravanan, P.; Singh, V. K.Tetrahedron Lett.1999,40, 2611.

[4]

Chandrasekhar S. Tetrahedron Lett. (1998) 10.1016/s0040-4039(98)00465-1

[5]

Damen E. W. P. Tetrahedron Lett. (1998) 10.1016/s0040-4039(98)01253-2

[6]

Orita A. J. Org. Chem. (1998) 10.1021/jo9800412

[7]

Breton G. W. J. Org. Chem. (1997) 10.1021/jo971367y

[8]

Orita A. Tetrahedron (1999) 10.1016/s0040-4020(99)00072-1

[9]

Karimi B. Synlett (2001) 10.1055/s-2001-12321

[10]

Iqbal J. J. Org. Chem. (1992) 10.1021/jo00033a020

[11]

Li T. S. J. Chem. Soc., Perkin Trans. 1 (1998)

[12]

Ballini R. Tetrahedron Lett. (1998) 10.1016/s0040-4039(98)01244-1

[13]

Bhaskar P. M. Tetrahedron Lett. (1998) 10.1016/s0040-4039(98)00178-6

[14]

Hofle G. Angew. Chem., Int. Ed. Engl. (1978) 10.1002/anie.197805691

[15]

Scriven E. F. V. Chem. Soc. Rev. (1983) 10.1039/cs9831200129

[16]

Vedejs E. J. Am. Chem. Soc. (1993) 10.1021/ja00061a056

[17]

Vedejs E. J. Org. Chem. (1993) 10.1021/jo00077a064

[18]

Ishihara K. J. Am. Chem. Soc. (1995) 10.1021/ja00129a047

[19]

Ishihara K. J. Org. Chem. (1996) 10.1021/jo952237x

[20]

Ishihara K. Synlett (1996) 10.1055/s-1996-5376

[21]

Barrett A. G. M. Chem. Commun. (1997) 10.1039/a606484a

[22]

Zhao H. J. Org. Chem. (1998) 10.1021/jo981161c

[23]

Orita A. Angew. Chem., Int. Ed. (2000) 10.1002/1521-3773(20000818)39:16<2877::aid-anie2877>3.0.co;2-v

[24]

Procopiou P. A. J. Org. Chem. (1998) 10.1021/jo980011z

[25]

Procopiou P. A. J. Chem. Soc., Chem. Commun. (1996) 10.1039/cc9960002625

[26]

Karimi B. J. Org. Chem. (2000) 10.1021/jo005519s

[27]

Karimi B. Org. Lett. (1999) 10.1021/ol9909987

[28]

Karimi B. Synlett (2000)

[29]

Karimi B. Chem. Lett. (1999) 10.1246/cl.1999.1199

[30]

Karimi B. Synlett (1999) 10.1055/s-1999-2835

[31]

Firouzabadi H. Synthesis (1999) 10.1055/s-1999-3679

[32]

Karimi B. Synlett (2000)

[33]

Karimi B. Synthesis (2002) 10.1055/s-2002-25775

[34]

Karimi B. Synlett (2002) 10.1055/s-2002-19764

[35]

Firouzabadi H. Tetrahedron Lett. (1999) 10.1016/s0040-4039(99)00647-4

[36]

Firouzabadi H. Bull. Chem. Soc. Jpn. (2001) 10.1246/bcsj.74.2401

[37]

Karimi B. Tetrahedron Lett. (2002) 10.1016/s0040-4039(02)00892-4

[38]

Auge J. Tetrahedron Lett. (1996)

[39]

Lubineau A. J. Carbohydr. Chem. (1997) 10.1080/07328309708005745

[40]

Gauttret P. Synth. Commun. (1996) 10.1080/00397919608086745

[41]

Sandberg M. Tetrahedron Lett. (1998) 10.1016/s0040-4039(98)01309-4

[42]

Kochhar K. S. J. Org. Chem. (1983) 10.1021/jo00158a036

[43]

Tomita M. Chem. Pharm. Bull. (1963) 10.1248/cpb.11.1484

[44]

Wegscheider R. Monatsh. Chem. (1909) 10.1007/bf01517523

[45]

Preparation and spectral properties of benzylidene diacetates

Fillmore Freeman, Elaine Marie Karchefski

Journal of Chemical & Engineering Data 1977 10.1021/je60074a038

[46]

Scriabire I. Bull. Chem. Soc. Fr. (1961)

[47]

Michie J. K. Synthesis (1981) 10.1055/s-1981-29613

[48]

Deka N. J. Org. Chem. (1997) 10.1021/jo961741e

[49]

Aggarwal V. K. Synlett (1998) 10.1055/s-1998-1799

[50]

Karimi B. Synlett (2000)

Showing 50 of 63 references

Cited By

131

Bromodimethylsulfonium bromide: A useful reagent for acylation of alcohols, phenols, amines, thiols, thiophenols and 1,1-diacylation of aldehydes under solvent free conditions

Abu T. Khan, Samimul Islam · 2005

Journal of Molecular Catalysis A: C...

Metrics

131

Citations

63

References

Details

Published: May 09, 2003
Vol/Issue: 68(12)
Pages: 4951-4954

Authors

B

Babak Karimi

Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), P.O. Box 45195-159, Gava Zang, Zanjan, Iran karimi@iasbs.ac.ir

J

Jafar Maleki

Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), P.O. Box 45195-159, Gava Zang, Zanjan, Iran karimi@iasbs.ac.ir

Cite This Article

Babak Karimi, Jafar Maleki (2003). Lithium Trifluoromethanesulfonate (LiOTf) as a Recyclable Catalyst for Highly Efficient Acetylation of Alcohols and Diacetylation of Aldehydes under Mild and Neutral Reaction Conditions. The Journal of Organic Chemistry, 68(12), 4951-4954. https://doi.org/10.1021/jo026678+

Lithium Trifluoromethanesulfonate (LiOTf) as a Recyclable Catalyst for Highly Efficient Acetylation of Alcohols and Diacetylation of Aldehydes under Mild and Neutral Reaction Conditions

You May Also Like