Paper
RSC Advances
Y. Hanzawa, Tetrahedron Lett., 2007, 48, 835–839; (c)
A. Kumar, M. K. Gupta and M. Kumar, Tetrahedron Lett.,
2010, 51, 1582–1584.
8 H. Firouzabadi, N. Iranpoor and A. A. Jafari, Adv. Synth.
Catal., 2005, 347, 655–661.
9 (a) J. Otera, Esterication, Wiley-VCH, Weinheim, Germany,
2003; (b) J. Mulzer, Comprehensive Organic Synthesis, ed. B.
M. Trost and L. Fleming, Pergamon Press, Oxford, 1991,
vol. 6, p. 323.
References
1
2
3
M. Gawande, V. Bonifacio, R. Luque, P. Branco and
R. S. Varma, Chem. Soc. Rev., 2013, 42, 5522–5551.
J. H. Fendler and E. J. Fendler, Catalysis in Micellar and
Macromolecular Systems, Academic Press, London, 1975.
(a) I. V. Berezin, K. Martinek and A. K. Yatsimirskii, Russ.
Chem. Rev., 1973, 42, 787–802; (b) S. Tascioglu,
Tetrahedron, 1996, 52, 11113–11384.
4
(a) F. M. Menger, J. U. Rhee and H. K. Rhee, J. Org. Chem., 10 (a) Y. Liu, E. Ranucci, M. S. Lindblad and
1
975, 40, 3803–3805; (b) C. Larpent, E. Bernard, F. B. Menn
and H. Patin, J. Mol. Catal. A: Chem., 1997, 116, 277–288;
c) T. Dwars, U. Schmidt, C. Fischer, I. Grassert, R. Kempe,
R. Frçhlich, K. Drauz and G. Oehme, Angew. Chem., Int.
A. C. Albertsson, J. Polym. Sci., Part A: Polym. Chem.,
2001, 39, 2508–2519; (b) D. Shekhawat, K. Nagarajan,
J. E. Jackson and D. J. Miller, Appl. Catal., A, 2002, 223,
261–273.
(
Ed., 1998, 37, 2851–2853; (d) I. Grassert, U. Schmidt, 11 A. Orjuela, A. J. Yanez, A. Santhanakrishnan, C. T. Lira and
S. Ziegler, C. Fischer and G. Oehme, Tetrahedron:
Asymmetry, 1998, 9, 4193–4202.
(a) R. Selke, J. Holz, A. Riepe and A. Borner, Chem. – Eur. J.,
D. J. Miller, Chem. Eng. J., 2012, 188, 98–107.
12 Diversied Natural Products Inc.,
www.dnpworld.com.
http://
5
1
998, 4, 769–771; (b) K. Yonehara, T. Hashizume, K. Mori, 13 T. Higuchi, L. Eberson and J. D. McRae, J. Am. Chem. Soc.,
K. Ohe and S. Uemura, J. Org. Chem., 1999, 64, 5593–5598;
1967, 89, 3001–3304.
(
c) K. Yonehara, K. Ohe and S. Uemura, J. Org. Chem., 1999, 14 (a) K. Wilson and J. H. Clark, Pure Appl. Chem., 2000, 72,
6
4, 9381–9385; (d) M. S. Goedheijt, B. E. Hanson,
1313–1319; (b) J. H. Clark, Acc. Chem. Res., 2002, 35, 791–
797; (c) L. Gubicza, N. Nemestothy, T. Frater and K. Bela-
Bako, Green Chem., 2003, 5, 236–239.
J. N. H. Reek, P. C. J. Kamer and P. W. N. M. van Leeuwen,
J. Am. Chem. Soc., 2000, 122, 1650–1667.
6
7
(a) Y.-Y. Peng, Q.-P. Ding, Z. Li, P. G. Wang and J.-P. Cheng, 15 V. Budarin, J. H. Clark, R. Luque and D. J. Macquarrie, Chem.
Tetrahedron Lett., 2003, 44, 3871–3875; (b) H. A. Zayas, A. Lu,
Commun., 2007, 634–635.
D. Valade, F. Amir, Z. Jia, R. K. O'Reilly and M. J. Monteiro, 16 (a) V. Budarin, J. H. Clark, R. Luque, D. J. Macquarrie,
ACS Macro Lett., 2013, 2, 327–331.
(a) A. A. Jafari, F. Moradgholi and F. Tamaddon, Eur. J. Org.
Chem., 2009, 1249–1255; (b) A. Saito, J. Numaguchi and
A. Koutinas and C. Webb, Green Chem., 2007, 9, 992–995;
(b) V. Budarin, J. H. Clark, R. Luque and D. J. Macquarrie,
Chem. – Eur. J., 2007, 13, 6914–6919.
This journal is © The Royal Society of Chemistry 2014
RSC Adv., 2014, 4, 5152–5155 | 5155