[2]
Blickenstaff, R.T. Antitumor steroid; Academic Press Inc, 1992.
[4]
(a)Guthrie, J.P.; O’Leary, S. Organic reaction mechanisms. Can. J. Chem., 1975, 53, 2150.
(b)Dugas, H.; Malika, I.O.; Rocheblave, L. Peptidomimetics and artificial enzymes. Steroids, 2008, 73, 375.
[9]
Barthakur, M.G.; Borthakur, M.; Devi, P.; Sakia, C.J.; Saikia, A.; Bora, U.; Boruah, R.C. A novel and efficient lewis acid catalysed preparation of pyrimidines: microwave-promoted reaction of urea and β-formyl enamides. Synlett, 2007, 2007(2), 223-226.
[12]
Katritzky, A.R.; Gut, J. Advances in Heterocyclic Chemistry; Academic Press Inc: London, 1963, p. 189.
[13]
Carruthers, W. Some Modern Methods of Organic Synthesis, 2nd ed; Cambridge University Press: Cambridge, 1978. Carruthers, W. Cycloaddition Reactions in Organic Synthesis; Pergamon: Oxford, 1990.
[26]
Teize, L.F.; Schneider, G.; Wolfling, J.; Fecher, A.; Nobel, T.; Peterson, S.; Schuberth, I.; Wulff, C. A novel approach in drug discovery: synthesis of estrone–talaromycin natural product hybrids. Chem. Eur. J, 2000, 6, 3755.
[28]
Von, I. Scherlitz, Hofmann.; Dubs, M.; Krieg, R.; Schonecker, B.; Kluge, M.; Sicker, D. Hybridnaturstoffe: Synthese cyclischer hydroxamsäuren der estra‐1,3,5(10)‐trien‐reihe. Helv. Chim. Acta, 1997, 80, 2345-2351.
[31]
Tietze, L.F.; Schneider, G.; Wölfling, J.; Nöbel, T.; Wulff, C.; Schubert, I.; Rübeling, A. Efficient synthesis of a novel estrone‐ talaromycin hybrid natural product. Angew. Chem. Int. Ed. Engl., 1998, 37(18), 2469-2470.
[32]
Schneider, G.; Bottka, S.; Hackler, L.; Wolfling, J.; Sohar, P. Steroids, XLI. neighbouring group participation, X. neighbouring group participation and fragmentation during the solvolysis of the epimers of 3‐methoxy‐16. Ann. Chem., 1989, 263, 58.
[37]
Hamelin, J.; Bazureau, J-P.; Boullet, F.T. Microwaves in Organic Chemisry, 2nd ed.; A., Loupy., Ed.; Wiley-VCH, Weinheim: Germany, 2003. Hoz, A. dela; Diaz-Ortiz, A.; Moreno, A. Microwaves in organic synthesis. Thermal and non-thermal microwave effects. Chem. Soc. Rev, 2005, 34, 164. Oliver, Kappe C. Microwave dielectric heating in synthetic organic chemistry. hem. Soc. Rev, 2008, 37, 1127.
[38]
Giguere, R.J.; Bray, T.L.; Duncan, S.M.; Majetich, G. Application of commercial microwave ovens to organic synthesis. Tetrahedron Lett.,1986, 27, 4945. b) Gedye, R.; Smith, F.; Westaway, K.; Ali, H.; Baldisera, L.; Laberge, L.; Rousell, J. The rapid synthesis of organic compounds in microwave ovens. Tetrahedron Lett., 1986, 27, 279.
[39]
Oliver Kappe, C. Controlled microwave heating in modern organic synthesis.Chem., Int. Ed., 2005, 43, 6250. Oliver Kappe, C. Microwaves in organic and medicinal chemistry; Stadler, A. Wiley-VCH: Weinheim, 2005.
[40]
Loupy, A.; Bram, G. Sansoulet, Chemical syntheses by means of microwave digestion as a focused open-vessel system: Structural properties of oxides and hydroxides as powders. J. New J. Chem., 1992, 16, 233.
[42]
Diaz-Ortiz, A.; Langa, F.; de la Hoz, A.; Moreno, A. Cycloadditions under microwave irradiation conditions: Methods and applications. Eur. J. Org. Chem., 2000, 4, 3659.
[45]
Langa, F.; de la Cruz, P.; Espildora, E.; de la Hoz, A. Microwaves in organic synthesis. Thermal and non-thermal microwave effects., 2000, 9, 168.
[56]
Cotterill, I. C.; Usyatinsky, A. Y.; Arnold, J.M.; Clark, D. S.; Dordick, J.S.; Michels, P.C.; Khmelnitsky, Y. L. Microwave assisted combinatorial chemistry synthesis of substituted pyridines. Tetrahed. Lett., 39, 10, 5, 1998, 1117-1120.
[58]
Varma, R.S. Solvent-free organic syntheses on mineral supports using microwave irradiation. Clean Prod. Process., 1999, 132.
[59]
Varma, R.S. Astra Zeneca Research Foundation; Kavitha Printers: Bangalore, India, 2002.
[64]
Barreto.; Angélica de Fátima, S.; Vercillo, Otilie, E.; Andrade, C, Z. Microwave-assisted polymer chemistry: Heck-reaction, transesterification, Baeyer–Villiger oxidation, oxazoline polymerization, acrylamide, and porous materials. J. Braz. Chem. Soc., 2011, 22, 462.
[67]
Polshettiwar, V.; Nadagouda, M.N.; Aus Varma, R.S. Microwave-assisted chemistry: A rapid and sustainable route to synthesis of organics and nanomaterials. J. Chem., 2009, 62, 16.
[86]
Barthakur, M.G.; Hasib, A.; Gogoi, J.; Boruah, R.C. A convenient strategy for the annulation of aryl scaffold to A/B-ring steroids under microwave irradiation. Steroids, 2010, 75, 445.
[98]
Lill, J.R. Microwave assisted proteomics; RSC Publishing: Cambridge, 2009.
[100]
Zhao, H. Aqueous microwave assisted chemistry.; Cambridge: RSC Publishing,, 2010, 123.
[109]
Nicolaov, K.C.; Chen, S.I. The art of total synthesis through cascade reactions. Chem. Soc. Rev., 2009, 38, 2293.
[119]
Santa, S.; Rahman, M.; Roy, A.; Majee, A.; Hajra, A. Org. Chem. Int., 2014.
[123]
Gonzalez-Olvera, R.; Demare, P.; Regla, I.; Juaristi, E. pplication of (1S, 4S)-2, 5-diazabicyclo [2.2. 1] heptane derivatives in asymmetric organocatalysis: the Biginelli reaction. ARKIVOC, 2008, vi, 61.