References
- Breslow, R.; Maitra, U. Tetrahedron Lett. 1984, 25, 1239. https://doi.org/10.1016/S0040-4039(01)80122-2
- Breslow, R.; Maitra, U.; Rideout, D. Tetrahedron Lett. 1983, 24, 1901. https://doi.org/10.1016/S0040-4039(00)81801-8
- Rideout, D. C.; Breslow, R. J. Am. Chem. Soc. 1980, 102, 7816. https://doi.org/10.1021/ja00546a048
- Clark, J. H.; Macquarrie, D. In Handbook of Green Chemistry and Technology; Blackwell Publishers: Oxford, 2002.
- Anastas, P.; Eghbali, N. Chem. Soc. Rev. 2010, 39, 301. https://doi.org/10.1039/b918763b
- Anastas, P. T.; Warner, J. C. In Green Chemistry: Theory and Practice; Oxford University Press: New York, 1998.
- Leitner, W. Green Chem. 2009, 11, 603. https://doi.org/10.1039/b907013n
- Breslow, R. In Green Chemistry; Anastas, P. T., Williamson, T. C., Eds.; Oxford Press: New York, 1998; Chapter 13.
- DeSimone, J. M. Science 2002, 297, 799. https://doi.org/10.1126/science.1069622
- Horvath, I. T.; Anastas, P. T. Chem. Rev. 2007, 107, 2167. https://doi.org/10.1021/cr0783784
- Kumar, B. S. P. A.; Madhav, B.; Reddy, K. H. V.; Nageswar, Y. V. D. Tetrahedron Lett. 2011, 52, 2862. https://doi.org/10.1016/j.tetlet.2011.03.110
- Otto, S.; Engberts, J. B. F. N. Pure Appl. Chem. 2000, 72, 1365. https://doi.org/10.1351/pac200072071365
- Narayan, S.; Muldoon, J.; Finn, M. G.; Fokin, V. V.; Kolb, H. C.; Sharpless, K. B. Angew. Chem., Int. Ed. 2005, 44, 3275. https://doi.org/10.1002/anie.200462883
- Chanda, A.; Fokin, V. V. Chem. Rev. 2009, 109, 725. https://doi.org/10.1021/cr800448q
- Aplander, K.; Hidestal, O.; Katebzadeh, K.; Lindstorm, U. M. Green Chem. 2006, 8, 22. https://doi.org/10.1039/b513656c
- Liu, R.; Dong, C.; Liang, X.; Wang, X.; Hu, X. J. Org. Chem. 2005, 70, 729. https://doi.org/10.1021/jo048369k
- Stavber, G.; Zupan, M.; Jereb, M.; Stavber, S. Org. Lett. 2004, 6, 4973. https://doi.org/10.1021/ol047867c
- Lindstrom, U. M. In Organic Reactions in Water: Principles, Strategies and Applications; Wiley-Blackwell: Oxford, UK, 2007.
- Hailes, H. C. Org. Process Res. Dev. 2007, 11, 114. https://doi.org/10.1021/op060157x
- Lindstrom, U. M. Chem. Rev. 2002, 102, 2751. https://doi.org/10.1021/cr010122p
- Butler, R. N.; Coyne, A. G. Chem. Rev. 2010, 110, 6302. https://doi.org/10.1021/cr100162c
- Polshettiwar, V.; Varma, R. S. Green Chem. 2010, 12, 743. https://doi.org/10.1039/b921171c
- Khatik, G. L.; Kumar, R.; Chakraborti, A. K. Org. Lett. 2006, 8, 2433. https://doi.org/10.1021/ol060846t
- Azizi, N.; Aryanasab, F.; Torkiyan, L.; Ziyaei, A.; Saidi, M. R. J. Org. Chem. 2006, 71, 3634. https://doi.org/10.1021/jo060048g
- Breslow, R. Acc. Chem. Res. 1991, 24, 159. https://doi.org/10.1021/ar00006a001
- Otto, S.; Engberts, J. B. F. N. Org. Biomol. Chem. 2003, 1, 2809. https://doi.org/10.1039/b305672d
- Lindstrom, U. M.; Andersson, F. Angew. Chem., Int. Ed. 2006, 45, 548. https://doi.org/10.1002/anie.200502882
- Chandrasekhar, J.; Shariffskul, S.; Jorgensen, W. L. J. Phys. Chem. B 2002, 106, 8078. https://doi.org/10.1021/jp020326p
- Lubineau, A.; Auge, J. Top. Curr. Chem. 1999, 206, 1. https://doi.org/10.1007/3-540-48664-X_1
- Lubineau, A.; Auge, J.; Queneau, Y. Synthesis 1994, 741.
- Sheldon, R. A. J. Mol. Catal. A 1996, 107, 75. https://doi.org/10.1016/1381-1169(95)00229-4
- Li, C.-J. Chem. Rev. 2005, 105, 3095. https://doi.org/10.1021/cr030009u
- Fringuelli, F.; Pizzo, F.; Tortoioli, S.; Vaccaro, L. Org. Lett. 2005, 7, 4411. https://doi.org/10.1021/ol051582y
- Pirrung, M. C.; Das Sarma, K. J. Am. Chem. Soc. 2004, 126, 444. https://doi.org/10.1021/ja038583a
- Azoulay, S.; Manabe, K.; Kobayashi, S. Org. Lett. 2005, 7, 4593. https://doi.org/10.1021/ol051546z
- Manabe, K.; Limura, S.; Sun, X.-M.; Kobayashi, S. J. Am. Chem. Soc. 2002, 124, 11971. https://doi.org/10.1021/ja026241j
- Organic Synthesis in Water; Grieco, P. A., Ed.; Blackie Academic and Professional: London, 1998.
- Li, C.-J.; Chen, L. Chem. Soc. Rev. 2006, 35, 68. https://doi.org/10.1039/b507207g
- Breslow, R. Acc. Chem. Res. 2004, 37, 471. https://doi.org/10.1021/ar040001m
- Pirrung, M. C. Chem. -Eur. J. 2006, 12, 1312. https://doi.org/10.1002/chem.200500959
- Virkutyte, J.; Baruwati, B.; Varma, R. S. Nano Scale 2010, 2, 1109.
- Polshettiwar, V.; Varma, R. S. Tetrahedron 2010, 66, 1091. https://doi.org/10.1016/j.tet.2009.11.015
- Liu, X.-L.; Zhang, X.-M.; Yuan, W.-C. Tetrahedron Lett. 2011, 52, 903. https://doi.org/10.1016/j.tetlet.2010.12.060
- Azizi, N.; Torkiyan, L.; Saidi, M. R. Org. Lett. 2006, 8, 2079. https://doi.org/10.1021/ol060498v
- Wu, H.; Lin, W.; Wan, Y.; Xin, H.-Q.; Shi, D.- Q.; Shi, Y.-H.; Yuan, R.; Bo, R.-C.; Yin, W. J. Comb. Chem. 2010, 12, 31. https://doi.org/10.1021/cc9001179
- Krasovskaya, V.; Krasovskiy, A.; Bhattacharjya, A.; Lipshutz, B. H. Chem. Commun. 2011, 47, 5717. https://doi.org/10.1039/c1cc11087j
- Gogoi, S.; Dutta, M.; Gogoi, J.; Boruah, R. C. Tetrahedron Lett. 2011, 52, 813. https://doi.org/10.1016/j.tetlet.2010.12.036
- Kumar, D.; Kumar, N. M.; Patel, G.; Gupta, S.; Varma, R. S. Tetrahedron Lett. 2011, 52, 1983. https://doi.org/10.1016/j.tetlet.2011.02.069
- Xie, J.-W.; Li, P.; Wang, T.; Zhou, F.-T. Tetrahedron Lett. 2011, 52, 2379. https://doi.org/10.1016/j.tetlet.2011.02.093
- Ramesh, K.; Murthy, S. N.; Nageswar, Y. V. D. Tetrahedron Lett. 2011, 52, 2362. https://doi.org/10.1016/j.tetlet.2011.02.082
- El Kaim, L.; Grimaud, L.; Purumandla, S. R. Tetrahedron Lett. 2010, 51, 4962. https://doi.org/10.1016/j.tetlet.2010.07.058
- Palasz, A. Synthesis 2010, 4021.
- Kolla, S. R.; Lee, Y. R. Tetrahedron 2010, 66, 8938. https://doi.org/10.1016/j.tet.2010.09.050
- Shi, L.; Tu, Y.-Q.; Wang, M.; Zhang, F.-M.; Fan, C. A. Org. Lett. 2004, 6, 1001. https://doi.org/10.1021/ol049936t
- Ma, N.; Jiang, B.; Zhang, G.; Tu, S.-J.; Wever, W.; Li, G. Green Chem. 2010, 12, 1357. https://doi.org/10.1039/c0gc00073f
- Adib, M.; Sheikhi, E.; Kavoosi, A.; Bijanzadeh, H. R. Tetrahedron 2010, 66, 9263. https://doi.org/10.1016/j.tet.2010.09.032
- Zhu, J.; Bienayme, H. In Multicomponent Reactions; Wiley-VCH Weinheim: Germany, 2005.
- Malacria, M. Chem. Rev. 1996, 96, 289. https://doi.org/10.1021/cr9500186
- Schwier, T.; Sromek, A. W.; Yap, D. M.; Chernyak, D.; Gevorgyan, V. J. Am. Chem. Soc. 2007, 129, 9868. https://doi.org/10.1021/ja072446m
- Barluenga, J.; Jimenez-Aquino, A.; Valdes, C.; Aznar, F. Angew. Chem., Int. Ed. 2007, 46, 1529. https://doi.org/10.1002/anie.200604407
- Waldmann, H.; Kuhn, M.; Liu, W.; Kumar, K. Chem. Commun. 2008, 1211.
- de Meijere, A.; von Zezschwitz, P.; Braese, S. Acc. Chem. Res. 2005, 38, 413. https://doi.org/10.1021/ar980025r
- Tietze, L. F.; Brasche, G.; Gericke, K. In Domino Reactions in Organic Synthesis; Wiley-VCH Weinheim: Germany, 2006.
- Diguez-Vzquez, A.; Tzschucke, C. C.; Lam, W. Y.; Ley, S. V. Angew. Chem., Int. Ed. 2008, 47, 209. https://doi.org/10.1002/anie.200704595
- Arya, A. K.; Kumar, M. Green Chem. 2011, 13, 1332. https://doi.org/10.1039/c1gc00008j
- Tietze, L. F. Chem. Rev. 1996, 96, 115. https://doi.org/10.1021/cr950027e
- Trost, B. M. Acc. Chem. Res. 2002, 35, 695. https://doi.org/10.1021/ar010068z
- Wender, P. A.; Verma, V. A.; Paxton, T. J.; Pillow, T. H. Acc. Chem. Res. 2008, 41, 40. https://doi.org/10.1021/ar700155p
- Doemling, A. Chem. Rev. 2006, 106, 17. https://doi.org/10.1021/cr0505728
- D'Souza, D. M.; Mueller, T. J. J. Chem. Soc. Rev. 2007, 36, 1095. https://doi.org/10.1039/b608235c
- Polshettiwar, V.; Varma, R. S. Chem. Soc. Rev. 2008, 37, 1546. https://doi.org/10.1039/b716534j
- Shore, G.; Yoo, W.-J.; Li, C.-J.; Organ, M. G. Chem. Eur. J. 2010, 16, 126. https://doi.org/10.1002/chem.200902396
- Ganem, B. Acc. Chem. Res. 2009, 42, 463. https://doi.org/10.1021/ar800214s
- Padwa, A. Chem. Soc. Rev. 2009, 38, 3072. https://doi.org/10.1039/b816701j
- Hennequin, L. F.; Thomas, A. P.; Johnstone, C.; Stokes, E. S. E.; Plé, P. A.; Lohmann, J.-J. M.; Ogilvie, D. J.; Dukes, M.; Wedge, S. R.; Curwen, J. O.; Kendrew, J.; Lambert-van der Brempt, C. J. Med. Chem. 1999, 42, 5369. https://doi.org/10.1021/jm990345w
- Yu, Y.; Singh, S. K.; Liu, A.; Li, T.-K.; Liu, L. F.; La Voie, E. J. Bioorg. Med. Chem. 2003, 11, 1475. https://doi.org/10.1016/S0968-0896(02)00604-1
- Ruchelman, A. L.; Sing, S. K.; Ray, A.; Wu, X.; Yang, J. M.; Zhu, N.; Liu, A.; Liu, L. F.; LaVoie, E. J. Bioorg. Med. Chem. 2004, 12, 795. https://doi.org/10.1016/j.bmc.2003.10.061
- Sato, Y.; Suzuki, Y.; Yamamoto, K.; Kuroiwa, S.; Maruyama, S. JP2005/10494, WO 2005121105, 2005
- Saxena, V.; Maiti, S. K.; Kumar, N.; Sharma, A. K. Indian. J. Anim. Sci. 2008, 78, 1250.
- Barraja, P.; Diana, P.; Lauria, A.; Passananti, A.; Almerico, A. M.; Minnei, C.; Longu, S.; Congiu, D.; Musiu, C.; LaColla, P. Bioorg. Med. Chem. 1999, 7, 1591. https://doi.org/10.1016/S0968-0896(99)00096-6
- Gavini, E.; Juliano, C.; Mulu, A.; Pirisino, G.; Murineddu, G.; Pinna, G. A. Arch. Pharm. 2000, 333, 341. https://doi.org/10.1002/1521-4184(200010)333:10<341::AID-ARDP341>3.0.CO;2-U
- Pattan, S. R.; Ali, M. S.; Pattan, J. S.; Redd, V. V. K. Ind. J. Heterocycl. Chem. 2004, 14, 157.
- Narayana, B.; Ra, K. K.; Ashalatha, K. K.; Kumari, N. S. Ind. J. Chem. 2006, 45B, 1704.
- Choudhari, B. P.; Mulwad, V. V. Ind. J. Chem. 2006, 45B, 309.
- Vikas, S.; Darbhamulla, S. Afr. Health Sci. 2009, 9, 275.
- Shaban, M. A.; Al Badry, O. M.; Kamala, A. M.; el Wahap Abd El-Gawad, M. A. J. Chem. Res. 2008, 715.
- Vargas, F.; Zoltan, T.; Rivas, C.; Ramirez, A.; Cordero, T.; Díaz, Y.; Izzo, C.; Cárdenas, Y. M.; López, V.; Gómez, L.; Ortega, J.; Fuentes, A. J. Photochem. Photobiol. B: Biol. 2008, 92, 83. https://doi.org/10.1016/j.jphotobiol.2008.05.001
- Ryu, C.-K.; Lee, J. Y. Bioorg. Med. Chem. Lett. 2006, 16, 1850 https://doi.org/10.1016/j.bmcl.2006.01.005
- Ramalingam, P.; Ganapaty, S.; Babu Rao, Ch.; Ravi, T. K. Indian J. Heterocycl. Chem. 2006, 15, 359.
- Lunniss, C.; Eldred, C.; Aston, N.; Craven, A.; Gohil, K.; Judkins, B.; Keeling, S.; Ranshaw, L.; Robinson, E.; Shipley, T.; Trivedi, N. Bioorg. Med. Chem. Lett. 2010, 20, 137. https://doi.org/10.1016/j.bmcl.2009.11.010
- Mitsumori, T.; Bendikov, M.; Sedo, J.; Wudl, F. Chem. Mater. 2003, 15, 3759. https://doi.org/10.1021/cm0340532
- Chapoulaud, V. G.; Plé, N.; Turck, A.; Queguiner, G. Tetrahedron 2000, 56, 5499. https://doi.org/10.1016/S0040-4020(00)00448-8
- Busch, A.; Turck, A.; Nowicka, K.; Barasella, A.; Andraud, C.; Plé, N. Heterocycles 2007, 71, 1723. https://doi.org/10.3987/COM-06-10984
- Haider, N.; Holzer, W. Sci. Synth. 2004, 16, 251.
- Vinogradova, O. V.; Balova, I. A. Chem. Heterocycl. Comp. 2008, 44, 501. https://doi.org/10.1007/s10593-008-0070-0
- Alajarin, M.; Bonillo, B.; Marin-Luna, M.; Vidal, A.; Orenes, R.-A. J. Org. Chem. 2009, 74, 3558. https://doi.org/10.1021/jo900304a
- Jiang, B.; Hao, W.-J.; Zhang, J.-P.; Tu, S.-J.; Shi, F. Org. Biomol. Chem. 2009, 7, 1171. https://doi.org/10.1039/b817930a
- Hasegawa, K.; Kimura, N.; Arai, S.; Nishida, A. J. Org. Chem. 2008, 73, 6363. https://doi.org/10.1021/jo8010864
- Vinogradova, O. V.; Sorokoumov, V. N.; Vasilevskii, S. F.; Balovaa, I. A. Russ. Chem. Bull. 2008, 57, 1725. https://doi.org/10.1007/s11172-008-0228-z
- Ichikawa, J.; Wada, Y.; Kuroki, H.; Miharab, J.; Nadanob, R. Org. Biomol. Chem. 2007, 5, 3956. https://doi.org/10.1039/b712965c
- Vinogradova, O. V.; Sorokoumov, V. N.; Vasilevsky, S. F.; Balova, I. A. Tetrahedron Lett. 2007, 48, 4907. https://doi.org/10.1016/j.tetlet.2007.05.055
- Vasilevsky, S. F.; Tretyakov, E. V.; Verkruijsse, H. D. Synth. Commun. 1994, 24, 1733. https://doi.org/10.1080/00397919408010177
- Vasilevsky, S. F.; Tretyakov, E. V. Liebigs Ann. Chem. 1995, 775.
- Alford, E. J.; Irving, H.; Marsh, H. S.; Schofield, K. J. Chem. Soc. 1952, 2991. https://doi.org/10.1039/jr9520002991
- Nunn, A. J.; Schofield, K. J. Chem. Soc. 1953, 3700. https://doi.org/10.1039/jr9530003700
- Pfannstiel, K.; Janecke, J. Ber. Dtsch. Chem. Ges. 1942, 75, 1096. https://doi.org/10.1002/cber.19420750911
- Baumgarten, H. E.; Anderson, C. H. J. Am. Chem. Soc. 1958, 80, 1981.
- Kanner, C. B.; Pandit, U. K. Tetrahedron 1981, 37, 3513. https://doi.org/10.1016/S0040-4020(01)98868-4
- Kiselyov, A. S. Tetrahedron Lett. 1995, 36, 1383. https://doi.org/10.1016/0040-4039(95)00005-W
- Domingues, C. Tetrahedron Lett. 1999, 40, 5111. https://doi.org/10.1016/S0040-4039(99)00949-1
- Shvartsberg, M. S.; Ivanchikova, I. D. Tetrahedron Lett. 2000, 41, 771. https://doi.org/10.1016/S0040-4039(99)02151-6
- Al-Awadi, N. A.; Elnagdi, M. H.; Ibrahim, Y. A.; Kaul, K.; Kumar, A. Tetrahedron 2001, 57, 1609 https://doi.org/10.1016/S0040-4020(00)01141-8
- Gomaa, M. A.-M. Tetrahedron Lett. 2003, 44, 3493. https://doi.org/10.1016/S0040-4039(03)00686-5
- Neber, P. W.; Kniller, G.; Herbst, K.; Trissler, H. A. Liebigs Ann. Chem. 1929, 471, 113. https://doi.org/10.1002/jlac.19294710106
- Alford, E. J.; Schofield, K. J. Chem. Soc. 1952, 2081. https://doi.org/10.1039/jr9520002081
- Chen, D.; Yang, C.; Xie, Y.; Ding, J. Heterocycles 2009, 77, 273. https://doi.org/10.3987/COM-08-S(F)7
- Kimball, D. B.; Haley, M. M. Angew. Chem., Int. Ed. 2002, 41, 3338. https://doi.org/10.1002/1521-3773(20020916)41:18<3338::AID-ANIE3338>3.0.CO;2-7
- Brase, S.; Dahmen, S.; Heuts, J. Tetrahedron Lett. 1999, 40, 6201. https://doi.org/10.1016/S0040-4039(99)01166-1
- Brase, S.; Gil, C.; Knepper, K. Bioorg. Med. Chem. 2002, 10, 2415. https://doi.org/10.1016/S0968-0896(02)00025-1
- Kimball, D. B.; Hayes, A. G.; Haley, M. M. Org. Lett. 2000, 2, 3825. https://doi.org/10.1021/ol006517x
- Kimball, D. B.; Weakley, T. J. R.; Herges, R.; Haley, M. M. J. Am. Chem. Soc. 2002, 124, 13463. https://doi.org/10.1021/ja027809r
- Kimball, D. B.; Weakley, T. J. R.; Haley, M. M. J. Org. Chem. 2002, 67, 6395. https://doi.org/10.1021/jo020229s
- Kimball, D. B.; Weakley, T. J. R.; Herges, R.; Haley, M. M. J. Am. Chem. Soc. 2002, 124, 1572. https://doi.org/10.1021/ja017227u
- Vinogradovaa, O. V.; Sorokoumova, V. N.; Balova, I. A. Tetrahedron Lett. 2009, 50, 6358. https://doi.org/10.1016/j.tetlet.2009.08.103
- Zeni, G.; Larock, R. C. Chem. Rev. 2006, 106, 4644. https://doi.org/10.1021/cr0683966
- Zeni, G.; Larock, R. C. Chem. Rev. 2004, 104, 2285. https://doi.org/10.1021/cr020085h
- Tsukamoto, H.; Kondo, Y. Org. Lett. 2007, 9, 4227. https://doi.org/10.1021/ol701776m
- Heller, S. T.; Natarajan, S. R. Org. Lett. 2007, 9, 4947. https://doi.org/10.1021/ol701784w
- Yang, M.; Zhang, X.; Lu, X. Org. Lett. 2007, 9, 5131. https://doi.org/10.1021/ol702503e
- Chernyak, N.; Tilly, D.; Li, Z.; Gevorgyan, V. Chem. Commun. 2010, 46, 150. https://doi.org/10.1039/b919991h
- Zhu, C.; Yamane, M. Tetrahedron 2011, 67, 4933. https://doi.org/10.1016/j.tet.2011.04.079
- Khalafy, J.; Rimaz, M.; Panahi, L.; Rabiei, H. Bull. Korean Chem. Soc. 2011, 32, 2428. https://doi.org/10.5012/bkcs.2011.32.7.2428
- Rimaz, M.; Khalafy, J. Arkivoc. 2010, (ii), 110.
- Rimaz, M.; Khalafy, J.; Najafi Moghadam, P. Aust. J. Chem. 2010, 63, 1396. https://doi.org/10.1071/CH09602
- Rimaz, M.; Noroozi Pesyan, N.; Khalafy, J. Magn. Reson. Chem. 2010, 48, 276. https://doi.org/10.1002/mrc.2573
- Rimaz, M.; Khalafy, J.; Noroozi Pesyan, N.; Prager, R. H. Aust. J. Chem. 2010, 63, 507.
- Altomare, C.; Cellamare, S.; Summo, L.; Catto, M.; Carotti, A.; Thull, U.; Carrupt, P.-A.; Testa, B.; Stoeckli-Evans, H. J. Med. Chem. 1998, 41, 3812. https://doi.org/10.1021/jm981005y
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