A green synthesis of isoquinolines using Ru(II)/peg-400 as homogeneous recyclable catalyst via C-H/N-N bond activation

Publish Year: 1399
نوع سند: مقاله ژورنالی
زبان: English
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JR_AJGC-4-2_004

تاریخ نمایه سازی: 1 مرداد 1399

Abstract:

A novel and green synthesis of 1-phenyl isoquinoline derivatives has been developed using [Ru(p-cymene)Cl2]2, as a homogeneous recyclable catalyst, with Cu(OAc)2 and AgSbF6 as oxidant and additive respectively, in PEG-400 biodegradable and green solvent via C-H/N-N functionalization of 1-(diphenylmethylene) hydrazine and aryl substituted acetylene. This protocol gives a simple extraction procedure, biodegradable and green solvent, high atom economy, reusable catalytic system and wide substrate scope with high yield of the product for the synthesis of isoquinoline derivatives.

Authors

Shrinivas L. Nakkalwar

Department of Chemistry, L. B. S. Mahavidyalaya, Dharmabad, Dist. Nanded, MS, India

Hanmant M. Kasralikar

Department of Chemistry, Shri Muktanand Mahavidyalaya, Gangapur,Dist. Aurangabad MS, India

Nitish S. Kaminwar

Department of Chemistry, L. B. S. Mahavidyalaya, Dharmabad, Dist. Nanded, MS, India

Shivaji B. Patwari

Department of Chemistry, L. B. S. Mahavidyalaya, Dharmabad, Dist. Nanded, MS, India

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  • .  Jemi J., Neethu V., Shebina P.R., Supriya A., Vidushi ...
  • . Chrzanowska M., Rozwadowska M.D. Chem. Rev., 2004, 104:3341 ...
  • . Giri P., Kumar G.S. Mini-Rev. Med. Chem., 2010, 10:568 ...
  • . Pawar A.B., Agarwal D., Lade D.M. J. Org. Chem., ...
  • . Zeni G., Larock R.C. Chem. Rev., 2004, 104:228 ...
  • . Nakamura I., Yamamoto Y., Chem. Rev., 2004, 104:2127 ...
  • . Roesch K.R., Larock R.C. J. Org. Chem. 1998, 63:5306 ...
  • . Huang Q., Hunter J.A., Larock R.C. Org. Lett., 2001, ...
  • . Roesch K.R., Zhang H., Larock R.C. J. Org. Chem., ...
  • . Korivi R.P., Cheng C.H. Org. Lett., 2005, 7:5179 ...
  • . Korivi R.P., Wu W.J., Cheng C.H. Chem. A Eur. ...
  • . Korivi R.P., Wu W.J., Cheng C.H. Chem. A Eur. ...
  • . Colby D.A., Bergman R.G., Ellman J.A. Chem. Rev., 2010, ...
  • . Cho S.H., Kim J.Y., Kwak J., Chang S. Chem. ...
  • . Ackermann L. Chem. Rev., 2011, 111:1315 ...
  • . Wencel-Delord J., Dröge T., Liu F., Glorius F. Chem. ...
  • . Arockiam P.B., Bruneau C., Dixneuf  P.H., Chem. Rev., 2012, ...
  • . Wencel-Delord J., Glorius F. Nat. Chem., 2013, 5:369 ...
  • . Shin K., Kim H., Chang S. Acc. Chem. Res., ...
  • . Ackermann L. Org. Process Res. Dev., 2015, 19:260 ...
  • . He R., Huang Z.T., Zheng Q.Y., Wang C. Tetrahedron ...
  • . Kulkarni A., Daugulis O. Synth., 2009, 4087 ...
  • . Nakao Y. Chem. Rec., 2011, 11:242 ...
  • . Miao J., Ge H. Eur. J. Org. Chem., 2015, ...
  • . Liu W., Ackermann L. Catal., 2016, 6:3743 ...
  • . Sun B., Yoshino T., Kanai M., Matsunaga S. Angew. ...
  • . Wang H., Koeller J., Liu W., Ackermann L. Chem. ...
  • . Sen M., Kalsi D., Sundararaju B. Chem. Eur. J. ...
  • . Muralirajan K., Kuppusamy R., Prakash S., Cheng C.H. Adv. ...
  • . Zhang S.S., Liu X.G., Chen S.Y., Tan D.H., Jiang ...
  • . Li J., Tang M., Zang L., Zhang X., Zhang ...
  • . Wang F., Wang Q., Bao M., Li X. Chin. ...
  • . Thansandote P., Lautens M. Chem. A Eur. J., 2009, ...
  • . Satoh T., Miura M. Chem. A Eur. J. 2010, ...
  • . Satoh T., Miura M. Synth., 2010, 20:3395 ...
  • . Colby D.A., Bergman R.G., Ellman J.A. Chem. Rev., 2010, ...
  • . Lim S.G., Lee J.H., Moon C.W., Hong C.J.B., Jun ...
  • . Parthasarathy  K., Jeganmohan M., Cheng C.H. Org. Lett., 2008, ...
  • . Parthasarathy K., Cheng C.H. J. Org. Chem., 2009, 74:9359 ...
  • . Parthasarathy K., Cheng  C.H. Synth., 2009, 8:1400 ...
  • . Colby D.A., Bergman R., Ellman J.A. J. Am. Chem. ...
  • . Martin R.M., Bergman R.G., Ellman J.A. J. Am. Chem. ...
  • . Guimond N., Fagnou K. J. Am. Chem. Soc., 2009, ...
  • . Fukutani T., Umeda N., Hirano K., Satoh T., Miura ...
  • . Jayakumar J., Parthasarathy K., Cheng C.H. Angew. Chem. Int. ...
  • . Too P.C., Wang Y.F., Chiba S. Org. Lett., 2010, ...
  • . Too P.C., Chua S.H., Wong S.H., Chiba S. J. ...
  • . Wang Y.F., Toh K.K., Lee J.Y., Chiba S. Angew. ...
  • . Ackermann L., Lygin A.V., Hofmann N. Angew. Chem. Int. ...
  • . Ackermann L., Lygin A.V., Hofmann N. Org. Lett., 2011, ...
  • . Ackermann L., Fenner S. Org. Lett., 2011, 13:6548 ...
  • . Li B., Feng H., Xu S., Wang B. Chem. ...
  • . Ackermann L., Wang L., Lygin A.V. Chem. Sci., 2012, ...
  • . Ackermann L., Lygin A.V. Org. Lett. 2012, 14:764 ...
  • . Ackermann L., Pospech J., Graczyk K., Rauch K. Org. ...
  • . Hashimoto Y., Hirano K., Satoh T., Kakiuchi F., Miura ...
  • . Ravi K.C., Sandeep P., Masilamani J. Org. Lett., 2012, ...
  • . Rajendran M., Masilamani T., Masilamani J. Org. Lett, 2017, ...
  • . Deshmukh D.S., Bhanage B.M. Org. Biomol. Chem., 2018, 16:4864 ...
  • . Zhang S., Huang D., Xu G., Cao S., Wang ...
  • . Qiu L., Huang D., Xu G., Dai Z., Sun ...
  • . Zhang S.S., Liu X.G., Chen S.Y., Tan D.H., Jiang ...
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