References
- Zhu, J.; Bienayme, H. Multicomponent Reactions; Wiley-Weinheim, 2005.
- Bayat, M.; Imanieh, H.; Zabarjad Shiraz, N.; Shah Qavidel, M. Monatsh Chem. 2010, 141, 333. https://doi.org/10.1007/s00706-010-0257-9
- Yavari, I.; Mirzaei, A.; Hossaini, Z.; Souri, S. Mol Divers. 2010, 14, 343.
- Ramazani, A.; Zeinali Nasrabadi, F.; Karimi, Z.; Rouhani, M. Bull. Korean Chem. Soc. 2011, 32, 2700. https://doi.org/10.5012/bkcs.2011.32.8.2700
- Ramazani, A.; Rezaei, A.; Mahyari, A. T.; Rouhani, M.; Khoobi, M. Helv. Chim. Acta. 2010, 93, 2033. https://doi.org/10.1002/hlca.201000057
- Ramazani, A.; Mahyari, A. Helv. Chim. Acta. 2010, 93, 2203. https://doi.org/10.1002/hlca.201000124
- Ramazani, A.; Mahyari, A. T.; Rouhani, M.; Rezaei, A. Tetrahedron Lett. 2009, 50, 5625. https://doi.org/10.1016/j.tetlet.2009.07.115
- Ramazani, A.; Shajari, N.; Mahyari, A.; Ahmadi, Y. Mol. Divers. 2011, 15, 521. https://doi.org/10.1007/s11030-010-9275-0
- Ramazani, A.; Nasrabadi, F. Z.; Mashhadi Malekzadeh, A.; Ahmadi, Y. Monatsh Chem. 2011, 142, 625. https://doi.org/10.1007/s00706-011-0488-4
- Yavari, I.; Sabbaghan, M.; Hossaini, Z. Mol. Divers. 2007, 11, 1. https://doi.org/10.1007/s11030-006-9052-2
- Yavari, I.; Hossaini, Z.; Sabbaghan, M. Mol. Divers. 2006, 10, 479. https://doi.org/10.1007/s11030-006-9034-4
- Domling, A. Chem. Rev. 2006, 106, 17. https://doi.org/10.1021/cr0505728
- Ugi, I.; Werner, B.; Dömling, A. Molecules 2003, 8, 53. https://doi.org/10.3390/80100053
- Waller, R. W.; Diorazio, L. J.; Taylor, B. A.; Motherwell, W. B.; Sheppard, T. D. Tetrahedron. 2010, 66, 6496. https://doi.org/10.1016/j.tet.2010.05.083
- Ramazani, A.; Ahmadi, Y.; Rouhani, M.; Shajari, N.; Souldozi, A. Heteroatom. Chem. 2010, 21, 368. https://doi.org/10.1002/hc.20626
- Ramazani, A.; Ahmadi, Y.; Tarasi, R. Heteroatom. Chem. 2011, 22, 79. https://doi.org/10.1002/hc.20660
- Souldozi, A.; S´ lepokura, K.; Lis, T.; Ramazani, A. Z. Naturforsch. 2007, 62b, 835.
- Ramazani, A.; Rezaei, A. Org. Lett. 2010, 12, 2852. https://doi.org/10.1021/ol100931q
- Ramazani, A.; Shajari, N.; Tofangchi Mahyari, A.; Khoobi, M.; Ahmadi, Y.; Souldozi, A. Phosphorus. Sulfur. Silicon Relat. Elem. 2010, 185, 2496. https://doi.org/10.1080/10426501003713098
- Stolzenberg, H.; Weinberger, B.; Fehlhammer, W. P.; Pühlhofer, F. G.; Weiss, R. Eur. J. Inorg. Chem. 2005, 21, 4263.
- Ramazani, A.; Bodaghi, A. Tetrahedron. Lett. 2000, 41, 567. https://doi.org/10.1016/S0040-4039(99)02066-3
- Pakravan, P.; Ramazani, A.; Noshiranzadeh, N.; Sedrpoushan, A. Phosphorus. Sulfur. 2007, 182, 545. https://doi.org/10.1080/10426500601013257
- Ramazani, A.; Rahimifard, M.; Souldozi, A. Phosphorus. Sulfur. 2007, 182, 1. https://doi.org/10.1080/10426500600961571
- Ramazani, A.; Rahimifard, M.; Noshiranzadeh, N.; Souldozi, A. Phosphorus. Sulfur. 2007, 182, 413. https://doi.org/10.1080/10426500600920007
- Ramazani, A.; Ahmadi, E.; Kazemizadeh, A. R.; Dolatyari, L.; Noshiranzadeh, N.; Eskandari, I.; Souldozi, A. Phosphorus. Sulphur. 2005, 180, 2419. https://doi.org/10.1080/104265090921137
- Ramazani, A.; Shajari, N.; Gouranlou, F. Phosphorus. Sulfur. 2001, 174, 223. https://doi.org/10.1080/10426500108040246
- Ramazani, A.; Amini, I.; Massoudi, A. Phosphorus. Sulphur. 2006, 181, 2225. https://doi.org/10.1080/10426500600614683
- Souldozi, A.; Ramazani, A.; Bouslimani, N.; Welter, R. Tetrahedron. Lett. 2007, 48, 2617. https://doi.org/10.1016/j.tetlet.2007.02.010
- Souldozi, A.; Ramazani, A. Tetrahedron. Lett. 2007, 48, 1549. https://doi.org/10.1016/j.tetlet.2007.01.021
- Souldozi, A.; Ramazani, A. Phosphorus. Sulfur. 2009, 184, 3191. https://doi.org/10.1080/10426500802705537
- Souldozi, A.; Ramazani, A. Phosphorus. Sulfur. 2009, 184, 2344. https://doi.org/10.1080/10426500802466684
- Souldozi, A.; Ramazani, A. Arkivoc. 2008, 16, 235.
Cited by
- The Reaction of Thioacids with α-Haloketones in Water: an Environmentally Green Synthesis of Thioester Derivatives vol.188, pp.9, 2013, https://doi.org/10.1080/10426507.2012.740704
- -Sulfonyl Azides vol.358, pp.7, 2015, https://doi.org/10.1002/adsc.201500829
- N–N bond formation in Ugi processes: from nitric acid to libraries of nitramines vol.53, pp.13, 2017, https://doi.org/10.1039/C6CC10288C
- N-Isocyaniminotriphenylphosphorane (Ph3PNNC) as an Efficient Reagent for the Synthesis of Fully Substituted 1,3,4-Oxadiazoles from 3-Phenyl-2-Propynoic Acid, Secondary Amines and Aromatic Bis-Aldehyde vol.188, pp.7, 2012, https://doi.org/10.1080/10426507.2012.717142
- The Ugi–Smiles and Passerini–Smiles Couplings: A Story About Phenols in Isocyanide‐Based Multicomponent Reactions vol.2014, pp.35, 2012, https://doi.org/10.1002/ejoc.201402783
- Synthesis of N-acylurea derivatives from carboxylic acids and N,N′-dialkyl carbodiimides in water vol.127, pp.12, 2015, https://doi.org/10.1007/s12039-015-0988-6
- Highly Stereoselective Synthesis of Natural‐Product‐Like Hybrids by an Organocatalytic/Multicomponent Reaction Sequence vol.127, pp.26, 2015, https://doi.org/10.1002/ange.201412074
- Highly Stereoselective Synthesis of Natural‐Product‐Like Hybrids by an Organocatalytic/Multicomponent Reaction Sequence vol.54, pp.26, 2012, https://doi.org/10.1002/anie.201412074