Another Successful Application of Newly Prepared GO-SiC3-NH3-H2PW as Highly Efficient Nanocatalyst for Fast Synthesis of Tetrahydrobenzo[b]pyrans

سال انتشار: 1400
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 231

فایل این مقاله در 10 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_AJCS-4-1_007

تاریخ نمایه سازی: 31 فروردین 1400

چکیده مقاله:

In this work, the newly prepared functionalized graphene oxide (GO), denoted as GO-SiC3-NH3-H2PW, was found as an effective nanocatalyst for a one-pot reaction of dimedone, aryl aldehydes, and malononitrile, giving rise to tetrahydrobenzo[b]pyran derivatives. The reactions were conducted in water, giving the corresponding products in 88-98% yields over 4-15 min. Other advantages of the method include cheap catalyst, easy work-up, absence of any dangerous solvents and the catalyst's reusability for up to five consecutive runs (97, 96, 95, 95, and 94 in first to fifth use, respectively).

نویسندگان

Zahra Hoseini

Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran

Abdolghasem Davoodnia

Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran

Mehdi Pordel

Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran

مراجع و منابع این مقاله:

لیست زیر مراجع و منابع استفاده شده در این مقاله را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود مقاله لینک شده اند :
  • [1] S. Sajjadifar, S. Rezayati, Chem. Pap., 2014, 68, 531–539. ...
  • [2] A. Fihri, C. Len, R.S. Varma, A. Solhy, Coord. ...
  • [3] A. Davoodnia, R. Mahjoobin, N. Tavakoli-Hoseini, Chin. J. Catal., ...
  • [4] P. Hu, M. Long, Appl. Catal. B., 2016, 181, ...
  • [5] E. kazemi, A. Davoodnia, A. Nakhaei, S. Basafa, N. ...
  • [6] M.M. Heravi, H. Hamidi, N. Karimi, A. Amouchi, Adv. ...
  • [7] M. Rohaniyan, A. Davoodnia, S.A. Beyramabadi, A. Khojastehnezhad, Appl. ...
  • [8] J. Zhao, Y. Xie, D. Hu, D. Guan, J. ...
  • [9] S. Kumari, A. Shekhar, D.D. Pathak, RSC Adv., 2014, ...
  • [10] N. Shang, C. Feng, H. Zhang, S. Gao, R. ...
  • [11] W.S. Hummers, R.E. Offeman, J. Am. Chem. Soc., 1958, ...
  • [12] J. Zhang, Y. Yang, J. Fang, G.-J. Deng, H. ...
  • [13] M. Shaikh, S.K. Singh, S. Khilari, M. Sahu, K.V.S. ...
  • [14] J. Zhang, S. Li, G.-J. Deng, H. Gong, ChemCatChem, ...
  • [15] S. Bhattacharya, P. Ghosh, B. Basu, Tetrahedron Lett., 2018, ...
  • [16] M. Coroş, F. Pogăcean, L. Măgeruşan, C. Socaci, S. Pruneanu, ...
  • [17] H. Ahmad, M. Fan, D. Hui, Composites Part B, ...
  • [18] J. Zhao, Y. Xie, J. Fang, Y. Ling, Y. ...
  • [19] J. Li, H. Xu, Talanta, 2017, 167, 623–629. ...
  • [20] M. Keyhaniyan, A. Shiri, H. Eshghi, A. Khojastehnezhad, New ...
  • [21] A. Khojastehnezhad, M. Bakavoli, A. Javid, M.M. Khakzad Siuki, ...
  • [22] A. Khojastehnezhad, M. Bakavoli, A. Javid, M.M. Khakzad Siuki, ...
  • [23] H. Su, Z. Li, Q. Huo, J. Guan, Q. ...
  • [24] P.K. Khatri, S. Choudhary, R. Singh, S.L. Jain, O.P. ...
  • [25] S. Kumari, A. Shekhar, D.D. Pathak, RSC Adv., 2016, ...
  • [26] D.R. Dreyer, S. Park, C.W. Bielawski, R.S. Ruoff, Chem. ...
  • [27] S. Verma, M. Aila, S. Kaul, S.L. Jain, RSC ...
  • [28] S. Omidi, A. Kakanejadifard, F. Azarbani, J. Mol. Liq., ...
  • [29] E. Kowsari, M.R. Chirani, Carbon, 2017, 118, 384–392. ...
  • [30] Y. Wu, Z. Zhao, M. Chen, Z. Jing, F. Qiu, Monatsh. Chem., 2018, ...
  • [31] Z. Ghadamyari, A. Khojastehnezhad, S.M. Seyedi, A. Shiri, ChemistrySelect, ...
  • [32] E. Doustkhah, S. Rostamnia, J. Colloid Interface Sci., 2016, 478, ...
  • [33] S. Rayati, E. Khodaei, S. Shokoohi, M. Jafarian, B. ...
  • [34] M.A. Mar’yasov, V.P. Sheverdov, V.V. Davydova, O.E. Nasakin, Pharm. Chem. ...
  • [35] I. Fatima, R. Saxena, G. Kharkwal, M.K. Hussain, N. ...
  • [36] A.E.F.G. Hammam, O.I. Abd El-Salam, A.M. Mohamed, N.A. Hafez, ...
  • [37] I.J.S. Fairlamb, L.R. Marrison, J.M. Dickinson, F.J. Lu, J.P. ...
  • [38] K. Rehse, W. Schinkel, Arch. Pharm., 1983, 316, 988–994. ...
  • [39] R.R. Kumar, S. Perumal, P. Senthilkumar, P. Yogeeswari, D. ...
  • [40] L. Bonsignore, G. Loy, D. Secci, A. Calignano, Eur. ...
  • [41] D. Armetso, W.M. Horspool, N. Martin, A. Ramos, C. ...
  • [42] S. Hatakeyama, N. Ochi, H. Numata, S. Takano, J. ...
  • [43] R.S. Bhosale, C.V. Magar, K.S. Solanke, S.B. Mane, S.S. ...
  • [44] M. Amirnejad, M.R. Naimi-Jamal, H. Tourani, H. Ghafuri, Monatsh. ...
  • [45] S. Nemouchi, R. Boulcina, B. Carboni, A. Debache, C. ...
  • [46] S. Gurumurthi, V. Sundari, R. Valliappan, E. J. Chem., ...
  • [47] S. Rathod, B. Arbad, M. Lande, Chin. J. Catal., ...
  • [48] F. Shirini, M. Safarpoor, N. Langarudi, J. Mol. Liq., 2017, ...
  • [49] L.M. Wang, J.H. Shao, H. Tian, Y.H. Wang, B. ...
  • [50] R. Mozafari, F. Heidarizadeh, Polyhedron, 2019, 162, 263–276. ...
  • [51] B. Maleki, H. Eshghi, M. Barghamadi, N. Nasiri, A. Khojastehnezhad, S.S. Ashrafi, O. ...
  • [52] B. Maleki, N. Nasiri, R. Tayebee, A. Khojastehnezhad, H.A. ...
  • [53] M. Hajjami, F. Gholamian, R.H.E. Hudson, A.M. Sanati, Catal. Lett., 2019, 149, ...
  • [54] J.T. Li, W.Z. Xu, L.C. Yang, T.S. Li, Synth. ...
  • [55] I. Devi, P.J. Bhuyan, Tetrahedron Lett., 2004, 45, 8625–8627. ...
  • [56] S. Khaksar, A. Rouhollahpour, S. Mohammadzadeh Talesh, J. Fluorine ...
  • [57] R. Hekmatshoar, S. Majedi, K. Bakhtiari, Catal. Commun., 2008, ...
  • [58] J. Zheng, Y. Li, Mendeleev Commun., 2011, 21, 280–281. ...
  • [59] Z. Hoseini, A. Davoodnia, A. Khojastehnezhad, M. Pordel, Eurasian ...
  • [60] A. Davoodnia, M. Khashi, N. Tavakoli-Hoseini, Chin. J. Catal., ...
  • [61] M. Rohaniyan, A. Davoodnia, A. Nakhaei, Appl. Organomet. Chem., ...
  • [62] A. Davoodnia, A. Nakhaei, N. Tavakoli-Hoseini, Z. Naturforsch., 2016, ...
  • [63] M. Fattahi, A. Davoodnia, M. Pordel, Russ. J. Gen. ...
  • [64] F. Tajfirooz, A. Davoodnia, M. Pordel, M. Ebrahimi, A. ...
  • [65] A. Davoodnia, M. Bakavoli, E. Imannezhad, N. Tavakoli-Hoseini, Indian ...
  • [66] M. Khashi, A. Davoodnia, V.S. Prasada Rao Lingam, Res. ...
  • [67] S. Vazirimehr, A. Davoodnia, M. Nakhaei-Moghaddam, N. Tavakoli-Hoseini, Heterocycl. ...
  • [68] N. Dorostkar-Ahmadi, A. Davoodnia, N. Tavakoli-Hoseini, H. Behmadi, Indian ...
  • [69] N. Dorostkar-Ahmadi, A. Davoodnia, N. Tavakoli-Hoseini, H. Behmadi, Z. ...
  • [70] A. Chanda, V.V. Fokin, Chem. Rev., 2009, 109, 725–748. ...
  • [71] C.I. Herrerias, X. Yao, Z. Li, C.J. Li, Chem. ...
  • [72] S. Ribe, P. Wipf, Chem. Commun., 2001, 4, 299–307. ...
  • نمایش کامل مراجع