Oxidative esterification of primary alcohols at room temperature under aqueous medium

References

• Otera, J.; Nishikido, J. Esterification: Methods, Reactions, and Applications; Wiley: Hoboken, NJ, 2009; p 1.
   Google Scholar
• (a) Biermann, U.; Metzger, J. O.; Meier, M. A. R. Macromol. Chem. Phys. 2010, 211, 854 (b) Biermann, U.; Bornscheuer, U.; Meier, M. A. R.; Metzger, J. O.; Schäfer, H. J. Angew. Chem. Int. Ed. 2011, 50, 3854.
   Web of Science ®Google Scholar
• (a) Bouzidi, L.; Li, S.; Di Biase, S.; Rizvi, S. Q.; Narine, S. S. Chem. Phys. Lipids 2012, 165, 38; (b) Bouzidi, L.; Li, S. J.; Di Biase, S.; Rizvi, S. Q.; Dawson, P.; Narine, S. S. Ind. Eng. Chem. Res. 2012, 51, 14892 (c) Bouzidi, L.; Li, S.; Di Biase, S.; Rizvi, S. Q.; Narine, S. S. Ind. Eng. Chem. Res. 2013, 52, 2740; (d) Bouzidi, L., Li, S., Narine, S., Symmetry 2014, 6, 655.
   PubMed Web of Science ®Google Scholar
• (a) Islam, A.; Ravindra, P. Biodiesel Production with Green Technologies; Springer, Cham, 2017; pp 1–105; (b) Pacheco, B. S.; Silva, C. C. D.; Freitas, S. C. D.; Berneira, L. M.; da Silva, V. L.; Winkel, K.; Ferreira, L. B.; de Pereira, C. M. P. Employment of Alternative Raw Materials for Biodiesel Synthesis; Springer: Cham, 2018; p 33; (c) Anzenberger, C.; Li, S.; Bouzidi, L.; Narine, S. S. Ind. Crops Prod. 2016, 89, 368.
   Google Scholar
• (a) Otera, J. Chem. Rev. 1993, 93, 1449–1470; (b) Larock, R. C. Comprehensive Organic Transformations: A Guide to Functional Group Preparations; Wiley-VCH: New York, 1999; Vol. 1, pp 1–2640; (c) Chau, K. D.; Duus, F.; Le, T. N. Green Chem. Lett. Rev. 2013, 6, 89; (d) Nguyen, J. D.; D’Amato, E. M.; Narayanam, J. M.; Stephenson, C. R. Nat. Chem. 2012, 4, 854; (e) Sun, H. B.; Hua, R.; Yin, Y. Molecules 2006, 11, 263.
   Google Scholar
• (a) Gunanathan, C.; Shimon, L. J. W.; Milstein, D. J. Am. Chem. Soc. 2009, 131, 3146; (b) Zhang, J.; Leitus, G.; David, Y. B.; Milstein, D. J. Am. Chem. Soc. 2005, 127, 10840; (c) Zhong, W.; Liu, H.; Bai, C.; Liao, S.; Li, Y. ACS Catal. 2015, 5, 1850; (d) Wang, F.; Xiao, Q.; Han, P.; Sarina, S.; Zhu, H. J. Mol. Catal. A Chem. 2016, 423, 61; (e) Jagadeesh, R. V.; Junge, H.; Pohl, M. M.; Radnik, J.; Bruckner, A.; Beller, M. J. Am. Chem. Soc. 2013, 135, 10776; (f) Gowrisankar, S.; Neumann, H.; Beller, M. Angew. Chem., Int. Ed. 2011, 50, 5139; (g) Moromi, S. K.; Siddiki, S. M. A. H.; Ali, M. A.; Kona, K.; Shimizu, K. I. Catal. Sci. Technol. 2014, 4, 3631.
   PubMed Web of Science ®Google Scholar
• (a) Minakawa, M.; Baek, H.; Yamada, Y. M. A.; Han, J. W.; Uozumi, Y. Org. Lett. 2013, 22, 5798; (b) Liu, X.; Wu, J.; Shang, Z. Synth. Commun. 2012, 42, 75; (c) Kajigaeshi, S.; Nakagawa, T.; Nagasaki, N.; Yamasaki, H.; Fujisaki, S. Bull. Chem. Soc. Jpn 1986, 597, 47; (d) Barluenga, J.; Francisco, G. B.; MurguÌa, M. C.; Ananthoju, S. R.; Gonzalez, J. M. Chem. Eur. 2004, 10, 4206; (e) Amati, A.; Dosualdo, G.; Zhao, L.; Bravo, A.; Fontana, F.; Minisci, F.; Bjørsvik, H. R. Org. Process. Res. Dev. 1998, 2, 261; (f) Chakraborti, A. K.; Singh, B.; Chankeshwara, S. V.; Patel, A. R. J. Org. Chem. 2009, 74, 5967.
   Web of Science ®Google Scholar
• (a) Arita, S.; Koike, T.; Kayaki, Y.; Ikariya, T. Chem. Asian J. 2008, 3, 1479; (b) Izumi, A.; Obora, Y.; Sakaguchi, S.; Ishii, Y. Tetrahedron Lett. 2006, 47, 9199; (c) Liu, C.; Wang, J.; Meng, L.; Deng, Y.; Li, Y. Lei, A. Angew. Chem., Int. Ed. 2011, 50, 5144; (d) Sunitha, S.; Kanjilal, S.; Reddy P. S.; Prasad R. B. N. Tetrahedron Lett. 2007, 48, 6962; (e) Tana, T.; Guo, X-W.; Xiao, Q.; Huang, Y.; Sarina, S.; Christopher, P.; Jia, J.; Wud, H.; Zhu, H. Chem. Commun. 2016, 52, 11567; (f) Toyao, T.; HakimSiddiki, S. M. A.; Touchy, A. S.; Onodera, W.; Kon, K.; Morita, Y.; Chi, T. K.; Yoshizawa, K.; Shimizu, K-I. Chem. Eur. J. 2017, 23, 1001.
   PubMed Web of Science ®Google Scholar
• (a) Nielsen, I. S.; Taarning, E.; Egeblad, K.; Madsen, R.; Christensen, C. H. Catal. Lett. 2007, 116, 35; (b) Su, F. N.; Ni, J.; Sun, H.; Cao, Y.; He H. Y.; Fan, K. N. Chem. Eur. J. 2008, 14, 7131; (c) Oliveira, R. L.; Kiyohara, P. K.; Rossi, L. M. Green Chem. 2009, 11, 1366; (d) Miyamura, H.; Yasukawa, T.; Kobayashi, S. Green Chem. 2010, 12, 776; (e) Suzuki, K.; Yamaguchi, T.; Matsushita, K.; Iitsuka, C.; Miura, J.; Akaogi, T.; Ishida, H. ACS Catal. 2013, 3, 1845; (f) Powell, A. B.; Stahl, S. S. Org. Lett. 2013, 15, 5072; (g) Salam, N.; Banerjee, B.; Roy, A. S.; Mondal, P.; Roy, S.; Bhaumik, A.; Islam, S. M. Appl. Catal. A: Gen. 2014, 477, 184.
   Web of Science ®Google Scholar
• (a) Joshi, G.; Patil, R. D.; Adimurthy, S. RSC Adv. 2012, 2, 2235; (b) Samanta, S.; pappula, V.; Dinda, M.; Adimurthy, S. Org. Biomol. Chem. 2014, 12, 9453; (c) Reddy, N. N. K.; Adimurthy, S. NF No. 0023NF2016/IN (patent filed).
   Web of Science ®Google Scholar
• (a) Adimurthy, S.; Ramachandraiah, G.; Bedekar, A. V.; Ghosh, S.; Ranu, B. C.; Ghosh, P. K. Green Chem. 2006, 8, 916; (b) Adimurthy, S.; Ghosh, S.; Patoliya, P. U.; Ramachandraiah, G.; Agrawal, M. K.; Gandhi, M. R.; Upadhyay, S. C.; Ghosh, P. K.; Ranu, B. C. Green Chem. 2008, 10, 232.
   Web of Science ®Google Scholar
• (a) Patil, R. D.; Joshi, G.; Adimurthy, S.; Ranu, B. C. Tetrahedron Lett. 2009, 50, 2529; (b) Agrawal, M. K.; Adimurthy, S.; Ganguly, B.; Ghosh, P. K. Tetrahedron 2009, 65, 2791; (c) Joshi, G.; Bhadra, S.; Ghosh, S.; Agrawal, M. K.; Ganguly, B.; Adimurthy, S.; Ghosh, P. K.; Ranu, B. C. Ind. Eng. Chem. Res. 2010, 49, 1236; (d) Patil, R. D.; Joshi G.; Adimurthy, S. Ind. Eng. Chem. Res. 2010, 49, 8100; (e) Joshi, G.; Adimurthy, S. Ind. Eng. Chem. Res. 2011, 50, 12271; (f) Patil, R. D.; Bhadra, S.; Adimurthy, S.; Ranu, B. C. Synth. Commun. 2010, 40, 2922; (g) Adimurthy, S.; Patoliaya, P. U. Synth. Commun. 2007, 37, 1571.
   Web of Science ®Google Scholar