A Facile and environmental friendly method for C=N bond cleavage of imines using p-toluenesulfonic acid in solid State

Publish Year: 1395
نوع سند: مقاله ژورنالی
زبان: English
View: 283

This Paper With 9 Page And PDF Format Ready To Download

  • Certificate
  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

JR_ICC-5-2_004

تاریخ نمایه سازی: 2 مهر 1398

Abstract:

A simple, efficient and clean procedure has been developed for the cleavage of imines C=N bond. Deprotection of imines to their parent carbonyl and amine compounds was achieved using p-toluenesulfonic acid in the solid state condition at 25-45 ˚C. The salient features of this methodology are shorter reaction times, cheap processing, high yields of product and easy availability of the catalyst. These features make this method an attractive alternative to existing routes for deprotection of iminesA simple, efficient and clean procedure has been developed for the cleavage of imines C=N bond. Deprotection of imines to their parent carbonyl and amine compounds was achieved using p-toluenesulfonic acid in the solid state condition at 25-45 ˚C. The salient features of this methodology are shorter reaction times, cheap processing, high yields of product and easy availability of the catalyst. These features make this method an attractive alternative to existing routes for deprotection of imines

Authors

Gholamhassan Imanzadeh

Department of Chemistry, College of Basic Science, University of Mohaghegh Ardabili ۵۶۱۹۹-۱۱۳۶۷, Ardabil, Iran

Hamideh Vakili

Department of Chemistry, College of Basic Science, University of Mohaghegh Ardabili ۵۶۱۹۹-۱۱۳۶۷, Ardabil, Iran

مراجع و منابع این Paper:

لیست زیر مراجع و منابع استفاده شده در این Paper 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 Paper لینک شده اند :
  • P.G.M. Wuts, T.W. Greene, Green′s Protective Groups in Organic Synthesis, ...
  • P.J. Kocienski, Protecting Groups, Thieme: Stuttgart, 1994. ...
  • R.O.C. Norman, Principle of Organic Synthesis. Chapman and Hall: London, ...
  • D.J.A. Schedler, A.G. Godfrey, B. Ganem, Tetrahedron Lett., 1993, 34, ...
  • S.D. Sharma, P. Gogoi, M. Boruah, D. Konwar, Synth. Commun., ...
  • G. Rao, M. Philipp, J. Org. Chem., 1991, 56, 1505-1512. ...
  • J.C. Sheehan, V.J. Grenda, J. Am. Chem. Soc., 1962, 84, ...
  • J.N. Williams Jr, R.M. Jacobs, Biochem. Biophys. Res. Commun., 1966, ...
  • A.R. Khomutov, A.S. Shvetsov, J.J. Vepsäläinen, A.M. Kritzyn, Tetrahedron Lett., ...
  • C.G. Rao, A.S. Radhakrishna, B.B. Singh, S.P. Bhatnager, Synthesis, 1983, ...
  • J.R. Maloney, R.E. Lyle, J.E. Saavedra, G.G. Lyle, 1978, 212-213. ...
  • R. Polt, L. Szabo, J. Treiberg, Y. Li, V.J. Hruby, ...
  • H. Alper, S. Amaratunga, J. Org. Chem., 1982, 47, 3593-3595. ...
  • P. Gogoi, P. Hazarika, D. Konwar, J. Org. Chem., 2005, ...
  • M. Ghiaci, G.H. Imanzadeh, , Synth. Commun., 1998, 28, 2275-2280. ...
  • G.H. Imanzadeh, A.R. Hajipour, S.E Mallakpour, Synth. Commun., 2003, 33, ...
  • G.H. Imanzadeh, M.R. Zamanloo, H. Eskandari, K. Shayesteh, J. Chem. ...
  • G.H. Imanzadeh, A.R Mosavi Zare, A. Zare, A. Khalafinezhad, A. ...
  • G.H. Imanzadeh, F. Ahmadi, M. Zamanloo, Y. Mansoori, Molecules., 2010, ...
  • G.H. Imanzadeh, F. Kazemi, M. Zamanloo, Y. Mansoori, Ultrason Sonochem., ...
  • Dictionary of organic compounds; Chapman and Hall: London, 1996. ...
  • B.F. Mirjalili, M.A. Zolfigol, A. Bamoniri, Molecules., 2002, 7, 751-755. ...
  • I.O. Donkor, A. Gangiee, R.L. Kisliuk, Y. Gaumont, J. Heterocycl. ...
  • A. Vogel, Vogel,s Practical Organic Chemistry, 4th ed.; Longman Press: ...
  • نمایش کامل مراجع