References
- Foroumadi, A.; Samzadeh-Kermani, A.; Emami, S.; Dehghan, G.; Sorkhi, M.; Arabsorkhi, F.; Heidari, M. R.; Abdollahi, M.; Shafiee, A. Bioorg. Med. Chem. Lett. 2007, 17, 6764-6769 https://doi.org/10.1016/j.bmcl.2007.10.034
- Rajan, Y. C.; Kanakam, C. C.; Selvam, S. P.; Murugesan, K. Tetrahedron Lett. 2007, 48, 8562-8565 and further references cited therein https://doi.org/10.1016/j.tetlet.2007.09.097
- Basavaiah, D.; Bakthadoss, M.; Pandiaraju, S. Chem. Commun. 1998, 1639-1640
- Rajan, Y. C.; Kanakam, C. C. Tetrahedron Lett. 2008, 49, 3023-3026 https://doi.org/10.1016/j.tetlet.2008.02.124
- Das, B.; Chowdhury, N.; Damodar, K.; Banerjee, J. Chem. Pharm. Bull. 2007, 55, 1274-1276 https://doi.org/10.1248/cpb.55.1274
- Skouta, R.; Li, C.-J. Angew. Chem. Int. Ed. 2007, 46, 1117-1119 https://doi.org/10.1002/anie.200603495
- Nakamura, T.; Hara, O.; Tamura, T.; Makino, K.; Hamada, Y. Synlett 2005, 155-157
- Hodgetts, K. J. Tetrahedron 2005, 61, 6860-6870 https://doi.org/10.1016/j.tet.2005.04.047
- Kawasaki, M.; Toyooka, N.; Matsui, Y.; Tanaka, A.; Goto, M.; Kakuda, H.; Kawabata, S.; Kometani, T. Heterocycles 2005, 65, 761-765 https://doi.org/10.3987/COM-05-10347
- Grigg, R.; Liu, A.; Shaw, D.; Selvaratnam, S.; Woodall, D. E.; Yoganathan, G. Tetrahedron Lett. 2000, 41, 7125-7128 https://doi.org/10.1016/S0040-4039(00)01176-X
- Sosnovskikh, V. Y.; Irgashev, R. A.; Kodess, M. I. Tetrahedron 2008, 64, 2997-3004 https://doi.org/10.1016/j.tet.2008.01.076
- Biddle, M. M.; Lin, M.; Scheidt, K. A. J. Am. Chem. Soc. 2007, 129, 3830-3831 https://doi.org/10.1021/ja070394v
- Skouta, R.; Li, C.-J. Tetrahedron Lett. 2007, 48, 8343-8346 https://doi.org/10.1016/j.tetlet.2007.09.122
- Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891 https://doi.org/10.1021/cr010043d
- Kim, J. N.; Lee, K. Y. Curr. Org. Chem. 2002, 6, 627-645 https://doi.org/10.2174/1385272023374094
- Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 1481-1490 https://doi.org/10.5012/bkcs.2005.26.10.1481
- Singh, V.; Batra, S. Tetrahedron 2008, 64, 4511-4574 and further references cited therein https://doi.org/10.1016/j.tet.2008.02.087
- Kim, S. J.; Kim, H. S.; Kim, T. H.; Kim, J. N. Bull. Korean Chem. Soc. 2007, 28, 1605-1608 https://doi.org/10.5012/bkcs.2007.28.9.1605
- Kim, H. S.; Kim, S. H.; Kim, J. N. Bull. Korean Chem. Soc. 2007, 28, 1841-1843 https://doi.org/10.5012/bkcs.2007.28.10.1841
- Lee, H. S.; Kim, S. H.; Kim, T. H.; Kim, J. N. Tetrahedron Lett. 2008, 49, 1773-1776 https://doi.org/10.1016/j.tetlet.2008.01.058
- Kim, S. H.; Kim, K. H.; Kim, H. S.; Kim, J. N. Tetrahedron Lett. 2008, 49, 1948-1951 https://doi.org/10.1016/j.tetlet.2008.01.110
- Kim, S. J.; Lee, H. S.; Kim, J. N. Tetrahedron Lett. 2007, 48, 1069-1072 https://doi.org/10.1016/j.tetlet.2006.11.180
- Kim, S. C.; Lee, H. S.; Kim, J. N. Bull. Korean Chem. Soc. 2007, 28, 147-150 https://doi.org/10.5012/bkcs.2007.28.1.147
- Nemes, C.; Levai, A.; Patonay, T.; Toth, G.; Boros, S.; Halasz, J.; Adam, W.; Golsch, D. J. Org. Chem. 1994, 59, 900- 905 https://doi.org/10.1021/jo00083a035
- Mallik, A.; Chattopadhyay, F. Indian J. Chem. 1999, 38B, 889-892
- Mallik, A.; Chattopadhyay, F. Indian J. Chem. 2005, 44B, 1947-1949
- Chawla, H. M.; Sharma, S. K. Synth. Commun. 1990, 20, 301-306 https://doi.org/10.1080/00397919008052298
- Chawla, H. M.; Sharma, S. K. Bull. Soc. Chim. Fr. 1990, 127, 656-659
- Adam, W.; Halasz, J.; Levai, A.; Nemes, C.; Patonay, T.; Toth, G. Liebigs Ann. Chem. 1994, 795- 803
- Dhande, V. P.; Thakwani, P.; Marathe, K. G. Tetrahedron 1988, 44, 3015-3023
- Kirkiacharian, B. S.; Gomis, M. Synth. Commun. 2005, 35, 563-569 https://doi.org/10.1081/SCC-200049789
- Patonay, T.; Dinya, Z.; Levai, A.; Molnar, D. Tetrahedron 2001, 57, 2895-2907 https://doi.org/10.1016/S0040-4020(01)00142-9
- Hoshino, Y.; Takeno, N. Bull. Chem. Soc. Jpn. 1994, 67, 2873- 2875 https://doi.org/10.1246/bcsj.67.2873
- Tait, S.; Salvati, A. L.; Desideri, N.; Fiore, L. Antiviral Res. 2006, 72, 252-255 https://doi.org/10.1016/j.antiviral.2006.07.003
- Kirkiacharian, S.; Tongo, H. G.; Bastide, J.; Bastide, P.; Grenie, M. M. Eur. J. Med. Chem. 1989, 24, 541-546 https://doi.org/10.1016/0223-5234(89)90060-3
- Kim, J. H.; Kim, K. H.; Kim, J. H.; Yu, Y. S.; Kim, Y.-M.; Kim, K.-W.; Kwon, H. J. Biochem. Biophys. Res. Commun. 2007, 362, 848-852 https://doi.org/10.1016/j.bbrc.2007.08.100
- Krishnamoorthy, T. V.; Rajagopalan, K.; Balasubramanian, K. K. Tetrahedron Lett. 1985, 26, 1747-1748 https://doi.org/10.1016/S0040-4039(00)98328-X
- Ashok, D.; Pallavi, K.; Reddy, G. J.; Rao, K. S. Indian J. Heterocyclic Chem. 2006, 16, 95-96
- Ingle, T. R.; Phalnikar, N. L.; Bhide, B. V. J. Indian Chem. Soc. 1949, 26, 569-574
- Sangwan, N. K.; Kelkar, P. M.; Rastogi, S. N.; Anand, N. Indian J. Chem. 1985, 24B, 639-644
Cited by
- Synthesis of 2,2'-Dipyrryl Ketones from Pyrrole-2-carboxylic Acids with Trifluoroacetic Anhydride vol.34, pp.9, 2013, https://doi.org/10.5012/bkcs.2013.34.9.2604
- Ruthenium-Catalyzed C–H Activation of Salicylaldehyde and Decarboxylative Coupling of Alkynoic Acids for the Selective Synthesis of Homoisoflavonoids and Flavones pp.1523-7052, 2017, https://doi.org/10.1021/acs.orglett.7b03325
- ChemInform Abstract: Expedient Synthesis of 3-Benzoylflavones by PCC Oxidation of 3-Benzylideneflavanones. vol.40, pp.10, 2009, https://doi.org/10.1002/chin.200910126
- Domino Synthesis of 3‐Alkyliden‐2,3‐Dihydro‐4‐Quinolones vol.361, pp.5, 2019, https://doi.org/10.1002/adsc.201801490