References
- Henry, L. Bull. Soc. Chim. Fr. 1895, 13, 999
- Rosini, G. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, UK, 1999; Vol. 2, pp 321
- Pinnick, H. W. In Organic Reactions; Paquette, L. A., Ed.; Wiley: New York, 1990; Vol. 38, Chapter 3
- Norman, B. H.; Morris, M. L. Tetrahedron Lett. 1992, 33, 6803 https://doi.org/10.1016/S0040-4039(00)61780-X
- Kawabata, T.; Kiryu, Y.; Sugiure, Y.; Fuji, K. Tetrahedron Lett. 1993, 34, 5127 https://doi.org/10.1016/S0040-4039(00)60694-9
- Sasai, H.; Kim, W.-S.; Suzuki, T.; Shibasaki, M. Tetrahedron Lett. 1994, 35, 6123 https://doi.org/10.1016/0040-4039(94)88093-X
- Corey, E. J.; Zhang, F.-Y.; Angew. Chem., Int. Ed. 1999, 38, 1931 https://doi.org/10.1002/(SICI)1521-3773(19990712)38:13/14<1931::AID-ANIE1931>3.0.CO;2-4
- Grembecka, J.; Kafarski, P. Mini Rev. Med. Chem. 2001, 1, 133 https://doi.org/10.2174/1389557013406990
- Sohtome, Y.; Takemura, N.; Iguchi, T.; Hashimoto, Y.; Nagasawa, K. Synlett 2006, 144
- Klein, G.; Pandiaraju, S.; Reiser, O. Tetrahedron Lett. 2002, 43, 7503 https://doi.org/10.1016/S0040-4039(02)01768-9
- Ma, D.; Pan, Q.; Han, F. Tetrahedron Lett. 2002, 43, 9401 https://doi.org/10.1016/S0040-4039(02)02332-8
- Misumi, Y.; Matsumoto, K. Angew. Chem., Int. Ed. 2002, 41, 1031 https://doi.org/10.1002/1521-3773(20020315)41:6<1031::AID-ANIE1031>3.0.CO;2-K
- Hanessian, S.; Devasthale, P. V. Tetrahedron Lett. 1996, 37, 987 https://doi.org/10.1016/0040-4039(95)02359-3
- For a recent example of an enantioselective Henry reaction, see: Palomo, C.; Oiarbide, M.; Laso, A. Angew. Chem., Int. Ed. 2005, 44, 3881 https://doi.org/10.1002/anie.200463075
- Rosini, G.; Ballini, R. Synthesis 1988, 833
- Rosini, G. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 2, pp 321
- Shvekhgeimer, M. A. Russ. Chem. Rev. 1998, 67, 35 https://doi.org/10.1070/RC1998v067n01ABEH000285
- Luzzio, F. A. Tetrahedron 2001, 57, 915 https://doi.org/10.1016/S0040-4020(00)00965-0
- Dalko, P. I.; Moisan, L. Angew. Chem. Int. Ed. 2001, 40, 3726 https://doi.org/10.1002/1521-3773(20011015)40:20<3726::AID-ANIE3726>3.0.CO;2-D
- Toda, F. Acc. Chem. Res. 1995, 28, 480 https://doi.org/10.1021/ar00060a003
- Mezger, J. O. Angew. Chem., Int. Ed. 1998, 37, 2975 https://doi.org/10.1002/(SICI)1521-3773(19981116)37:21<2975::AID-ANIE2975>3.0.CO;2-A
- Tanaka, K.; Toda, F. Chem. Rev. 2000, 100, 1025 https://doi.org/10.1021/cr940089p
- Li, G.; Wei, H.-X.; Wills, S. Tetrahedron Lett. 1998, 39, 4607 https://doi.org/10.1016/S0040-4039(98)00850-8
- Ramachandran, P. V.; Reddy, M. V. R.; Rudd, M. T. Tetrahedron Lett. 1999, 40, 627 https://doi.org/10.1016/S0040-4039(98)02504-0
- Ramachandran, P. V.; Reddy, M. V. R.; Rudd, M. T. Chem. Commun. 1999, 1979
- Costa, M.; Chiusoli, G. P.; Taffurelli, D.; Dalmonego, G. J. Chem. Soc. Perkin Trans. 1 1998, 1541
- Kovacevic, B.; Maksic, Z. B. Org. Lett. 2001, 3, 1523 https://doi.org/10.1021/ol0158415
- Yamamota, Y.; Kojima, S. In The Chemistry of Amidines and Imidates; Patai, S.; Rappoport, Z., Eds.; Wiley: New York, 1991; Vol. 2, p 485
- Wei, T. B.; Lin, Q.; Zhang, Y. M.; Wang, H. Synth. Commun. 2004, 34, 12, 2205 https://doi.org/10.1081/SCC-120038502
- Chauhan, M.; Boudjouk, P. Can. J. Chem. 2000, 78, 1396 https://doi.org/10.1139/cjc-78-11-1396
- Nishiyama, H.; Furuta, A. Chem. Commun. 2007, 760
- Klein, G.; Pandiaraju, S.; Reiser, O. Tetrahedron Lett. 2002, 43, 7503 https://doi.org/10.1016/S0040-4039(02)01768-9
- Kim, S. S.; Song, D. H. Eur. J. Org. Chem. 2005, 1777
- Kim, S. S.; Lee, S. H. Synth. Commun. 2005, 35, 751 https://doi.org/10.1081/SCC-200050390
- Kim, S. S.; Lee, S. H.; Kwak, J. M. Tetrahedron Asymmetry 2006, 17, 1165 https://doi.org/10.1016/j.tetasy.2006.04.011
- Kim, S. S.; Kwak, J. M. Tetrahedron 2006, 62, 49 https://doi.org/10.1016/j.tet.2005.09.131
- Kim, S. S.; Rajagopal, G.; Song, D. H. J. Organomet. Chem. 2004, 689, 1734 https://doi.org/10.1016/j.jorganchem.2004.01.025
- Kim. S. S.; Kim, D. W.; Rajagopal, G. Synthesis 2004, 213
- Kim, S. S.; Rajagopal, G.; Kim, D. W.; Song, D. H. Synth. Commun. 2004, 34, 2973 https://doi.org/10.1081/SCC-200026652
- Kim, S. S.; George, S. C. Bull. Korean Chem. Soc. 2008, 29(7), 1167 https://doi.org/10.5012/bkcs.2008.29.6.1167
- Kadam, S. T.; Kim, S. S. Synthesis 2008, 267
- Kadam, S. T.; Kim, S. S. Catal. Commun. 2008, 9, 1342 https://doi.org/10.1016/j.catcom.2007.11.030
- Majhi, A.; Kim, S. S.; Kim, H. S. Applied Organometal. Chem. 2008, 22, 407 https://doi.org/10.1002/aoc.1416
- Majhi, A.; Kim, S. S.; Kadam, S. T. Tetrahedron 2008, 64, 5509 https://doi.org/10.1016/j.tet.2008.03.106
- Kadam S. T.; Kim, S. S. Bull. Korean Chem. Soc. 2008, 29(7), 1320 https://doi.org/10.5012/bkcs.2008.29.7.1320
- Weeden, A. J.; Chisholm, D. J. Tetrahedron Lett. 2006, 47, 9313 https://doi.org/10.1016/j.tetlet.2006.10.107
- Cwik, A.; Fuchs, A.; Hell, Z.; Clacens, J. M. Tetrahedron 2005, 61, 4015 https://doi.org/10.1016/j.tet.2005.02.055
- Hirata, N.; Hayashi, M. Synthetic Commun. 2007, 37, 1653 https://doi.org/10.1080/00397910701263833
- Han, J.; Xu, Y.; Su, Y.; She, X.; Pan, X. Catal. Commun. 2008, 9, 2077 https://doi.org/10.1016/j.catcom.2008.04.006
- Quin, B.; Xiao, X.; Liu, X.; Huang, J.; Wen, Y.; Feng, X. J. Org. Chem. 2007, 72, 9323 https://doi.org/10.1021/jo701898r
Cited by
- Biocatalytic Approaches to the Henry (Nitroaldol) Reaction vol.2012, pp.16, 2012, https://doi.org/10.1002/ejoc.201101840
- Resolution of 2-nitroalcohols by Burkholderia cepacia lipase-catalyzed enantioselective acylation vol.34, pp.1, 2012, https://doi.org/10.1007/s10529-011-0754-x
- The Henry Reaction in [Bmim][PF6]-based Microemulsions Promoted by Acylase vol.18, pp.11, 2013, https://doi.org/10.3390/molecules181113910
- ) metal–organic framework derived from a flexible amido tripodal acid vol.44, pp.22, 2015, https://doi.org/10.1039/C4DT03087G
- Catalytic insertion of aldehydes into dihalonitroacetophenones via sequential bond scission-aldol reaction-acyl transfer vol.52, pp.17, 2016, https://doi.org/10.1039/C5CC09753C
- Organocatalytic Insertion of Isatins into Aryl Difluoronitromethyl Ketones vol.82, pp.2, 2017, https://doi.org/10.1021/acs.joc.6b02704
- A new sustainable protocol for the synthesis of nitroaldol derivatives via Henry reaction under solvent-free conditions vol.7, pp.1, 2014, https://doi.org/10.1080/17518253.2014.893028
- ChemInform Abstract: TMEDA Catalyzed Henry (Nitroaldol) Reaction under Metal and Solvent-Free Conditions. vol.40, pp.51, 2009, https://doi.org/10.1002/chin.200951064
- Zinc metal–organic frameworks: efficient catalysts for the diastereoselective Henry reaction and transesterification vol.43, pp.21, 2009, https://doi.org/10.1039/c4dt00219a