Boron Trifluoride Ethyl Ether as an Effective Catalyst in the Synthesis of Alkyl p-Aminobenzoates

Kadaba, Pankaja K.; Carr, M. J.; Tribo, M.; Triplett, J. W.; Glasser, Arthur C.

doi:10.1002/jps.2600581131

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Cited by 27 publications

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“…DNSA was purchased from Sigma Chemical Co. (St. Louis, MO). n ‐Alkyl p ‐ABEs were synthesized by alkylation of p ‐aminobenzoic acid according to a conventional method,24 and their structures were confirmed by elemental analysis, melting point determination, and nuclear magnetic resonance. All other chemicals were of analytical grade.…”

Section: Methodsmentioning

confidence: 99%

Characterization of site I of human serum albumin using spectroscopic analyses: Locational relations between regions Ib and Ic of site I

Yamasaki

Maruyama

Takadate

et al. 2004

Journal of Pharmaceutical Sciences

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Section: Methodsmentioning

confidence: 99%

Characterization of site I of human serum albumin using spectroscopic analyses: Locational relations between regions Ib and Ic of site I

Yamasaki

Maruyama

Takadate

et al. 2004

Journal of Pharmaceutical Sciences

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Boron trifluoride etherate

Ho¹,

Fieser²,

Fieser³

et al. 2006

Fieser and Fieser's Reagents for Organic Synthesis

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The Lewis acid boron trifluoride etherate has played an important role in organic synthesis. To accomplish the hydroxylation of double bond, cleavage of epoxides, esterification of acids and many cyclization reaction boron trifluoride etherate proved very useful compared to other Lewis acids. These organic reactions are frequently employed to achieve the synthesis of natural products. In addition, boron trifluoride etherate has also been utilized to realize ketalization, thioketalization, alkylation and many others organic reactions.

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