References
- Page, P. Organosulfur Chemistry; Academic Press: London,1995.
- Kondo, T.; Mitsudo, T. Chem. Rev. 2000, 100, 3205. https://doi.org/10.1021/cr9902749
- Arisawa, M.; Yamaguchi, M. Pure Appl. Chem. 2008, 80, 993. https://doi.org/10.1351/pac200880050993
- Renaud, P.; Sibi, M. P. Radicals in Organic Synthesis;Wiley-VCH: Weinheim, 2001; Vol. 2. Chapter 5.5.3.
- Griesbaum,K. Angew. Chem., Int. Ed. Engl. 1970, 9, 273. https://doi.org/10.1002/anie.197002731
- Peach, M. E. In The Chemistry of the Thiol Group; Patai, S., Ed., Vol. 2, Wiley: London, 1974.
- Yorimitsu, H.; Wakabayashi, K.; Shinokubo, H.; Oshima, K. Bull. Chem. Soc. Jpn. 2001, 74, 1963. https://doi.org/10.1246/bcsj.74.1963
- Miyata, O.; Nakajima, E.; Naito,T. Chem. Pharm. Bull. 2001, 49, 213. https://doi.org/10.1248/cpb.49.213
- Friestad, G. K.; Jiang,T.; Fioromi, G. M. Tetrahedron Asymmetry 2003, 14, 2853. https://doi.org/10.1016/S0957-4166(03)00540-8
- Beaufils, F.; Denes, F.; Renaud, P. Org. Lett. 2004, 6, 2563. https://doi.org/10.1021/ol049162g
- Benati, L.; Leardini, R.; Minozzi, M.; Nanni, D.; Scialpi, R.; Spagnolo,P.; Zanardi, G. Synlett 2004, 987.
- Beaufils, F.; Denes, F.;Becattini, B.; Renaud, P.; Schenk, K. Adv. Synth. Catal. 2005, 347,1587. https://doi.org/10.1002/adsc.200505211
- Yasuda, H.; Uenoyama, Y.; Nobuta, O.; Kobayashi, S.;Ryu, I. Tetrahedron Lett. 2008, 49, 367. https://doi.org/10.1016/j.tetlet.2007.11.039
- Bencivenni, G.; Lanza,T.; Leardini, R.; Minozzi, M.; Nanni, D.; Spagnolo, P.; Zanardi, G.Org. Lett. 2008, 10, 1127. https://doi.org/10.1021/ol800046k
- Rahaman, H.; Ueda, M.; Miyata, O.;Naito, T. Org. Lett. 2009, 11, 2651. https://doi.org/10.1021/ol900604a
- Wadsworth, D. H.; Detty, M. R. J. Org. Chem. 1980, 45, 4611. https://doi.org/10.1021/jo01311a013
- Benati, L.; Montevecchi, P. C.; Spagnolo, P. J. Chem. Soc., Perkin Trans. 1 1991, 2103.
- Montevecchi, P. C.; Navacchia, M.L.; Spagnolo, P. Eur. J. Org. Chem. 1998, 1219
- Montevecchi, P. C.; Navacchia, M. L.; Spagnolo,P. Tetrahedron 1998, 54, 8207. https://doi.org/10.1016/S0040-4020(98)00458-X
- Fernandez-Gonzales, M.; Alonso,R. J. Org. Chem. 2006, 71, 6767. https://doi.org/10.1021/jo060883y
- Ichinose, Y.; Wakamatsu,K.; Nozaki, K.; Birbaum, J.-L.; Oshima, K.; Utimoto, K. Chem. Lett. 1987, 1647.
- Matteson, D. S.; Peacock,K. J. Org. Chem. 1963, 28, 369. https://doi.org/10.1021/jo01037a022
- Lhermitte, F.; Carboni, B. Synlett 1996, 377.
- Melandri, D.; Montevecchi,P. C.; Navacchia, M. L. Tetrahedron 1999, 55, 12227. https://doi.org/10.1016/S0040-4020(99)00699-7
- Zificsak, C. A.; Mulder, J. A.; Hsung, R. P.; Rameshkumar, C.;Wei, L.-L. Tetrahedron 2001, 57, 7575. https://doi.org/10.1016/S0040-4020(01)00681-0
- Mulder, J. A.; Kurtz, K.C. M.; Hsung, R. P. Synlett 2003, 1379.
- Witulski, B.; Stengel, T.Angew. Chem. Int. Ed. 1998, 37, 489. https://doi.org/10.1002/(SICI)1521-3773(19980302)37:4<489::AID-ANIE489>3.0.CO;2-N
- Sato, A.; Yorimitsu, H.;Oshima, K. Synlett 2009, 28.
- Marion,F.; Courillon, C.; Malacria, M. Org. Lett. 2003, 5, 5095. https://doi.org/10.1021/ol036177q
- Nozaki, K.; Oshima, K.; Utimoto, K. J. Am. Chem. Soc. 1987,109, 2547. https://doi.org/10.1021/ja00242a068
- Nozaki, K.; Oshima, K.; Utimoto, K. Bull. Chem. Soc. Jpn. 1987, 60, 3465. https://doi.org/10.1246/bcsj.60.3465
- Ito, O.; Fleming, M. D. C. M. J. Chem. Soc., Perkin Trans. 2 1989,689.
- Wille, U.; Dreessen, T. J. Phys. Chem. A 2006, 110, 2195. https://doi.org/10.1021/jp0454772
- Arnaud, R.; Barone, V.; Olivella, S.; Sole, A. Chem. Phys. Lett.1985, 118, 573. https://doi.org/10.1016/0009-2614(85)85356-2
- Galli, C.; Guarnieri, A.; Koch, H.; Mencarelli, P.; Rappoport, Z. J. Org. Chem. 1997, 62, 4072. https://doi.org/10.1021/jo962373h
- Kursaniov, D. N.; Parnes, Z. N.; Bassova, G. L.; Loim, N. M.; Zdanovich,V. I. Tetrahedron 1967, 23, 2235. https://doi.org/10.1016/0040-4020(67)80059-0
- Markgren, P.-O.; Schaal, W.; Hämäläinen, M.; Karlén, A.; Hallberg,A.; Samuelsson, B.; Danielson, U. H. J. Med. Chem. 2002, 45,5430. https://doi.org/10.1021/jm0208370
- Vargas, F.; Sehnem, J. A.; Galetto, F. Z.; Braga, A. L. Tetrahedron2008, 64, 392 https://doi.org/10.1016/j.tet.2007.10.086
- Jin, M.-J.;Sarkar, S. M.; Lee, D.-H.; Qiu, H. Org. Lett. 2008, 10, 1235 https://doi.org/10.1021/ol8001249
- Zhang, Y.; Hsung, R. P.; Tracey, M. R.; Kurtz, K. C. M.; Vera, E.L. Org. Lett. 2004, 6, 1151. https://doi.org/10.1021/ol049827e
Cited by
- Regio- and Stereoselective Synthesis of 2-Amino-1,3-diene Derivatives by Ruthenium-Catalyzed Coupling of Ynamides and Ethylene vol.13, pp.10, 2011, https://doi.org/10.1021/ol200812y
- sulfonyl Ynamides as Synthetic Precursors to Amidines and Vinylogous Amidines. An Unexpected N-to-C 1,3-Sulfonyl Shift in Nitrile Synthesis vol.76, pp.12, 2011, https://doi.org/10.1021/jo200780x
- Thiol–yne coupling: revisiting old concepts as a breakthrough for up-to-date applications vol.10, pp.19, 2012, https://doi.org/10.1039/c2ob25217a
- Radical Cascades Initiated by Intermolecular Radical Addition to Alkynes and Related Triple Bond Systems vol.113, pp.1, 2013, https://doi.org/10.1021/cr100359d
- Thiyl Radicals in Organic Synthesis vol.114, pp.5, 2014, https://doi.org/10.1021/cr400441m
- Palladium-Catalyzed Addition of 1,3-Diones to Ynamides: An Entry to Alkoxy-Substituted Enamides vol.6, pp.9, 2014, https://doi.org/10.1002/cctc.201402398
- Palladium-Catalyzed Oxidative Sulfamidation: A Stereoselective Synthesis for Enesulfonamides vol.359, pp.4, 2017, https://doi.org/10.1002/adsc.201601048
- Rhodium-Catalyzed Annulation of Ynamides with Bifunctional Arylboron Reagents vol.12, pp.11, 2010, https://doi.org/10.1021/ol100769p
- ChemInform Abstract: Radical Additions of Arenethiols to Ynamides for the Selective Synthesis of N-[(Z)-2-(Arylsulfanyl)-1-alkenyl]amides. vol.41, pp.32, 2010, https://doi.org/10.1002/chin.201032094
- BEt3‐Initiated Thiol–Ene Click Reactions as a Versatile Tool To Modify Sensitive Substrates vol.2015, pp.36, 2010, https://doi.org/10.1002/ejoc.201500915
- Intermolecular Addition of Carbon-Centered Radicals to Ynamides. A Regio- and Stereoselective Route to Persubstituted α-Iodo-enamides vol.85, pp.6, 2010, https://doi.org/10.1021/acs.joc.9b03255
- Ynamides in Free Radical Reactions vol.362, pp.22, 2010, https://doi.org/10.1002/adsc.202000849