English

• 

• 1. [1] A. Dömling, I. Ugi, Multicomponent reactions with isocyanides, Angew. Chem. Int. Ed. 39 (2000) 3168-3210.[1] A. Dömling, I. Ugi, Multicomponent reactions with isocyanides, Angew. Chem. Int. Ed. 39 (2000) 3168-3210.

  2. [2] V. Nair, R.S. Menon, V. Sreekumar, Multicomponent reactions based on nucleophilic carbenes and their applications in organic synthesis, Pure Appl. Chem. 77 (2005) 1191-1198.[2] V. Nair, R.S. Menon, V. Sreekumar, Multicomponent reactions based on nucleophilic carbenes and their applications in organic synthesis, Pure Appl. Chem. 77 (2005) 1191-1198.

  3. [3] A. Dömling, Recent developments in isocyanide based multicomponent reactions in applied chemistry, Chem. Rev. 106 (2006) 17-89.[3] A. Dömling, Recent developments in isocyanide based multicomponent reactions in applied chemistry, Chem. Rev. 106 (2006) 17-89.

  4. [4] G. Campiani, A. Garofalo, I. Fiorini, et al., Pyrrolo[2,1-c][1,4]benzothiazines: synthesis, structure-activity relationships, molecular modeling studies, and cardiovascular activity, J. Med. Chem. 38 (1995) 4393-4410.[4] G. Campiani, A. Garofalo, I. Fiorini, et al., Pyrrolo[2,1-c][1,4]benzothiazines: synthesis, structure-activity relationships, molecular modeling studies, and cardiovascular activity, J. Med. Chem. 38 (1995) 4393-4410.

  5. [5] D.S. Snyder, L. Tradtrantip, C. Yao, M.J. Kurth, A.S. Verkman, Potent, metabolically stable benzopyrimido-pyrrolo-oxazine-dione (BPO) CFTR inhibitors for polycystic kidney disease, J. Med. Chem. 54 (2011) 5468-5477.[5] D.S. Snyder, L. Tradtrantip, C. Yao, M.J. Kurth, A.S. Verkman, Potent, metabolically stable benzopyrimido-pyrrolo-oxazine-dione (BPO) CFTR inhibitors for polycystic kidney disease, J. Med. Chem. 54 (2011) 5468-5477.

  6. [6] X.Q. Xie, X.W. Han, J.Z. Chen, M. Eissenstat, A. Makriyannis, High-resolution NMR and computer modeling studies of a highly potent cannabimimetic ligand aminoalkyl indoles, J. Med. Chem. 42 (1999) 4021-4027.[6] X.Q. Xie, X.W. Han, J.Z. Chen, M. Eissenstat, A. Makriyannis, High-resolution NMR and computer modeling studies of a highly potent cannabimimetic ligand aminoalkyl indoles, J. Med. Chem. 42 (1999) 4021-4027.

  7. [7] M. Artico, G. Porretta, G. De Martino, The synthesis of 4H-pyrrole[2,1-c][1,4]benzoxazine, J. Heterocycl. Chem. 6 (1971) 283-287.[7] M. Artico, G. Porretta, G. De Martino, The synthesis of 4H-pyrrole[2,1-c][1,4]benzoxazine, J. Heterocycl. Chem. 6 (1971) 283-287.

  8. [8] G. Cheeseman, M. Rafiz, P.D. Roy, C. Turner, G.V. Boyd, Synthesis and reactions of pyrrolo[2,1-c][1,2,4]benzotriazine and 4-oxo-4H-pyrrolo[2,1-c][1,4]benzoxazine, J. Chem. Soc. C (1971) 2018-2022.[8] G. Cheeseman, M. Rafiz, P.D. Roy, C. Turner, G.V. Boyd, Synthesis and reactions of pyrrolo[2,1-c][1,2,4]benzotriazine and 4-oxo-4H-pyrrolo[2,1-c][1,4]benzoxazine, J. Chem. Soc. C (1971) 2018-2022.

  9. [9] I. Sanchez, M.D. Pujol, A convenient synthesis of pyrrolo[21-c][1,4] benzoxazines, Tetrahedron 55 (1999) 5593-5598.[9] I. Sanchez, M.D. Pujol, A convenient synthesis of pyrrolo[21-c][1,4] benzoxazines, Tetrahedron 55 (1999) 5593-5598.

  10. [10] S. Kurhade, R.D. Kaduskar, B. Dave, et al., Synthesis of a novel tetracyclic azaindolo[2,1-c][1,4]benzoxazine ring system, Tetrahedron Lett. 52 (2011) 1874-1877.[10] S. Kurhade, R.D. Kaduskar, B. Dave, et al., Synthesis of a novel tetracyclic azaindolo[2,1-c][1,4]benzoxazine ring system, Tetrahedron Lett. 52 (2011) 1874-1877.

  11. [11] I. Yavari, M. Piltan, L. Moradi, Synthesis of pyrrolo[2,1-a]isoquinolines from activated acetylenes, benzoylnitromethanes, and isoquinoline, Tetrahedron 65 (2009) 2067-2071.[11] I. Yavari, M. Piltan, L. Moradi, Synthesis of pyrrolo[2,1-a]isoquinolines from activated acetylenes, benzoylnitromethanes, and isoquinoline, Tetrahedron 65 (2009) 2067-2071.

  12. [12] M. Piltan, L. Moradi, H. Salimi, K. Zargoosh, S.A. Zarei, PEG-mediated catalyst-free expeditious synthesis of polysubstituted anilines and benzenes via the reaction of malononitrile and b-ketoester derivatives in the presence of activated acetylenes, Comb. Chem. High Throughput Screening 15 (2012) 571-575.[12] M. Piltan, L. Moradi, H. Salimi, K. Zargoosh, S.A. Zarei, PEG-mediated catalyst-free expeditious synthesis of polysubstituted anilines and benzenes via the reaction of malononitrile and b-ketoester derivatives in the presence of activated acetylenes, Comb. Chem. High Throughput Screening 15 (2012) 571-575.

  13. [13] L. Moradi, M. Piltan, H. Rostami, G. Abasi, One-pot synthesis of pyrrolo[1,2- a]pyrazines via three component reaction of ethylenediamine, acetylenic esters and nitrostyrene derivatives, Chin. Chem. Lett. 24 (2013) 740-742.[13] L. Moradi, M. Piltan, H. Rostami, G. Abasi, One-pot synthesis of pyrrolo[1,2- a]pyrazines via three component reaction of ethylenediamine, acetylenic esters and nitrostyrene derivatives, Chin. Chem. Lett. 24 (2013) 740-742.

  14. [14] M. Piltan, I. Yavari, L. Moradi, Tandem synthesis of functionalized hexaalkyl benzoisoquinolinopyrrolonaphthyridine-hexacarboxylate, via isoquinoline based multi-component reaction, Chin. Chem. Lett. 24 (2013) 979-983.[14] M. Piltan, I. Yavari, L. Moradi, Tandem synthesis of functionalized hexaalkyl benzoisoquinolinopyrrolonaphthyridine-hexacarboxylate, via isoquinoline based multi-component reaction, Chin. Chem. Lett. 24 (2013) 979-983.

•