Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2019; 30(06): 647-664
DOI: 10.1055/s-0037-1610340
DOI: 10.1055/s-0037-1610340
account
Rapid Formation of Advanced Scaffolds from Phenols and Anilines
We are grateful to the Natural Sciences and Engineering Research Council of Canada (NSERC), the Canada Foundation for Innovation (CFI), the provincial government of Quebec (FQRNT and CCVC) for their precious financial support in this research.Further Information
Publication History
Received: 08 August 2018
Accepted after revision: 25 October 2018
Publication Date:
11 December 2018 (online)
Abstract
This article is an account of our efforts over the last decade to functionalize phenols and anilines at any position and to use these compounds to generate substituted aromatic systems and advanced unsaturated cyclohexanone moieties, enabling the rapid formation of complex structures. Total syntheses of numerous natural products involving such intermediates were achieved.
1 Introduction
2 ortho-Functionalization of Phenols and Aniline Derivatives Mediated by Iodanes (III) and Synthesis of Panacene
2.1 Cross-Coupling with Aniline Derivatives
2.2 Dearomative Cycloaddition of Arenes and Heteroarenes
2.3 Total Synthesis of Panacene
3 meta-Functionalization of Aniline Derivatives and Synthesis of Erysotramidine
3.1 meta-Functionalization of Aniline Derivatives
3.2 Total Synthesis of Erysotramidine
4 para-Functionalization of Phenols and Applications in Total Synthesis
4.1 Bimolecular Approach Mediated by Protecting Groups
4.2 ipso-Rearrangement
4.3 Oxidative Alkyl Shift
4.4 Oxidative Prins-Pinacol Rearrangement
4.5 Oxidative Prins-Type Reaction
4.6 Total Synthesis of (–)-Fortucine
4.7 Total Synthesis of Isostrychnine
4.8 Total Synthesis of (–)-Strychnopivotine
5 Development of a Functional Protecting Group
-
References
- 1a Hypervalent Iodine Chemistry: Modern Developments in Organic Synthesis. 2003; 224
- 1b Ciufolini MA, Braun NA, Canesi S, Ousmer M, Chang J, Chai D. Synthesis 2007; 3759
- 1c Zhdankin VV, Stang PJ. Chem. Rev. 2008; 108: 5299
- 1d Liang H, Ciufolini MA. Chem. Eur. J. 2010; 16: 13262
- 1e Vanderlaan DG, Schwartz MA. J. Org. Chem. 1985; 50: 743
- 1f Lewis N, Wallbank P. Synthesis 1987; 1103
- 1g Gates BD, Dalidowicz P, Tebben A, Wang S, Swenton JS. J. Org. Chem. 1992; 57: 2135
- 1h Swenton JS, Callinan A, Chen Y, Rohde JJ, Kearns ML, Morrow GW. J. Org. Chem. 1996; 61: 1267
- 1i Braun NA, Ciufolini MA, Peters K, Peters EM. Tetrahedron Lett. 1998; 39: 4667
- 1j Quideau S, Looney MA, Pouységu L. Org. Lett. 1999; 1: 1651
- 1k Braun NA, Bray J, Ousmer M, Peters K, Peters EM, Bouchu D, Ciufolini MA. J. Org. Chem. 2000; 65: 4397
- 1l Scheffler G, Seike H, Sorensen EJ. Angew. Chem. Int. Ed. 2000; 39: 4593
- 1m Canesi S, Bouchu D, Ciufolini MA. Angew. Chem. Int. Ed. 2004; 43: 4336
- 1n Quideau S, Pouységu L, Oxoby M, Looney MA. Tetrahedron 2001; 57: 319
- 1o Canesi S, Belmont P, Bouchu D, Rousset L, Ciufolini MA. Tetrahedron Lett. 2002; 43: 5193
- 1p Quideau S, Pouységu L, Deffieux D. Curr. Org. Chem. 2004; 8: 113
- 1q Canesi S, Bouchu D, Ciufolini MA. Org. Lett. 2005; 7: 175
- 1r Honda T, Shigehisa H. Org. Lett. 2006; 8: 657
- 1s Nicolaou KC, Edmonds DJ, Li A, Tria GS. Angew. Chem. Int. Ed. 2007; 46: 3942
- 1t Silva LF. Jr, Siqueira FA, Pedrozo EC, Vieira FY. M, Doriguetto AC. Org. Lett. 2007; 9: 1433
- 1u Quideau S, Pouységu L, Deffieux D. Synlett 2008; 467
- 1v Liang H, Ciufolini MA. J. Org. Chem. 2008; 73: 4299
- 1w Giroux MA, Guérard KC, Beaulieu MA, Sabot C, Canesi S. Eur. J. Org. Chem. 2009; 3871
- 1x Peuchmaur M, Saıdani N, Botté C, Maréchal E, Vial H, Wong YS. J. Med. Chem. 2008; 51: 4870
- 1y Mendelsohn BA, Ciufolini MA. Org. Lett. 2009; 11: 4736
- 1z Jen T, Mendelsohn BA, Ciufolini MA. J. Org. Chem. 2011; 76: 728
- 1aa Traoré M, Ahmed-Ali S, Peuchmaur M, Wong YS. J. Org. Chem. 2011; 76: 1409
- 1ab Deruer E, Hamel V, Blais S, Canesi S. Beilstein J. Org. Chem. 2018; 14: 1203
- 2a Seebach D, Corey EJ. J. Org. Chem. 1975; 40: 231
- 2b Seebach D. Angew. Chem. Int. Ed. 1979; 18: 239
- 3a Tamura Y, Yakura T, Haruta J, Kita Y. J. Org. Chem. 1987; 52: 3927
- 3b Dohi T, Ito M, Yamaoka N, Morimoto K, Fujioka H, Kita Y. Tetrahedron 2009; 65: 10797
- 3c Dohi T, Takenaga N, Nakae T, Toyoda Y, Yamasaki M, Shiro M, Fujioka H, Maruyama A, Kita Y. J. Am. Chem. Soc. 2013; 135: 4558
- 3d Dohi T, Yamaoka N, Kita Y. Tetrahedron 2010; 66: 5775
- 3e Kita Y, Tohma H, Kikuchi K, Inagaki M, Yakura T. J. Org. Chem. 1991; 56: 435
- 4 Stuart DR, Fagnou K. Science 2007; 316: 1172
- 5 Jean A, Cantat J, Berard D, Bouchu D, Canesi S. Org. Lett. 2007; 9: 2553
- 6 Jacquemot G, Ménard MA, L’Homme C, Canesi S. Chem. Sci. 2013; 4: 1287
- 7 Ito M, Kubo H, Itani I, Morimoto K, Dohi T, Kita Y. J. Am. Chem. Soc. 2013; 135: 1478
- 8a Bérard D, Jean A, Canesi S. Tetrahedron Lett. 2007; 48: 8238
- 8b Guérard KC, Sabot C, Beaulieu MA, Giroux MA, Canesi S. Tetrahedron 2010; 66: 5893
- 8c Deruer E, Canesi S. Org. Biomol. Chem. 2017; 3736
- 9a Bérard D, Racicot L, Sabot C, Canesi S. Synlett 2008; 1076
- 9b Bérard D, Giroux M.-A, Racicot L, Sabot C, Canesi S. Tetrahedron 2008; 64: 7537
- 10 Sabot C, Bérard D, Canesi S. Org. Lett. 2008; 10: 4629
- 11a Kinnel R, Duggan AJ, Eisner T, Meinwald J, Miura I. Tetrahedron Lett. 1977; 18: 3913
- 11b Feldman KS, Mechem CC, Nader L. J. Am. Chem. Soc. 1982; 104: 4011
- 11c Feldman KS. Tetrahedron Lett. 1982; 23: 3031
- 11d Boukouvalas J, Pouliot M, Robichaud J, MacNeil S, Snieckus V. Org. Lett. 2006; 8: 3597
- 11e Alnafta N, Schmidt JP, Nesbitt CL, McErlean CS. P. Org. Lett. 2016; 18: 6520
- 12 Deruer E, Coulibali S, Boukercha S, Canesi S. J. Org. Chem. 2017; 11884
- 13 Giroux MA, Guérard KC, Beaulieu MA, Sabot C, Canesi S. Eur. J. Org. Chem. 2009; 3871
- 14a Ito K, Furukawa H, Haruna M. Yakugaku Zasshi 1973; 93: 1611
- 14b Mantle PG, Laws I, Widdowson DA. Phytochemistry 1984; 23: 1336
- 14c Tsuda Y, Sano T. In The Alkaloids . Vol. 48. Cordell GA. Academic Press; San Diego: 1996: 249
- 14d Boekelheide V. In The Alkaloids . Vol. 7. Manske RH. F. Academic Press; New York: 1960: 201
- 14e Hill RK. In The Alkaloids . Vol. 9. Manske RH. F. Academic Press; New York: 1967: 483
- 14f Dyke SF, Quessy SN. In The Alkaloids . Vol. 18. Rodrigo RG. A. Academic Press; New York: 1981: 1
- 14g Chawala AS, Jackson AH. Nat. Prod. Rep. 1984; 1: 371
- 15a Joo JM, David RA, Yuan Y, Lee C. Org. Lett. 2010; 12: 5704
- 15b Tuan LA, Kim G. Bull. Korean Chem. Soc. 2010; 31: 1800
- 15c Liang J, Chen J, Liu J, Li L, Zhang H. Chem. Commun. 2010; 46: 3666
- 15d Onoda T, Takikawa Y, Fujimoto T, Yasui Y, Suzuki K, Matsumoto T. Synlett 2009; 1041
- 15e Yoshida Y, Mohri K, Isobe K, Itoh T, Yamamoto K. J. Org. Chem. 2009; 74: 6010
- 15f Stanislawski PC, Willis AC, Banwell MG. Chem. Asian J. 2007; 2: 1127
- 15g Shimizu K, Takimoto M, Sato Y, Mori M. J. Organomet. Chem. 2006; 691: 5466
- 15h Stanislawski PC, Willis AC, Banwell MG. Org. Lett. 2006; 8: 2143
- 15i Kim G, Kim JH, Lee KY. J. Org. Chem. 2006; 71: 2185
- 15j Yasui Y, Suzuki K, Matsumoto T. Synlett 2004; 619
- 15k Fukumoto H, Esumi T, Ishihara J, Hatakeyama S. Tetrahedron Lett. 2003; 44: 8047
- 15l Shimizu K, Takimoto M, Mori M. Org. Lett. 2003; 5: 2323
- 15m Kalaitzakis D, Montagnon T, Antonatou E, Vassilikogiannakis G. Org. Lett. 2013; 15: 3714
- 15n Isobe K, Mohri K, Takeda N, Suzuki K, Hosoi S, Tsuda Y. Chem. Pharm. Bull. 1994; 42: 197
- 15o Tsuda Y, Hosoi S, Katagiri N, Kaneko C, Sano T. Chem. Pharm. Bull. 1993; 41: 2087
- 15p Tsuda Y, Hosoi S, Sano T, Suzuki H, Toda J. Heterocycles 1993; 36: 655
- 15q Isobe K, Mohri K, Suzuki K, Haruna M, Ito K, Hosoi S, Tsuda Y. Chem. Pharm. Bull. 1991; 32: 1195
- 15r Tsuda Y, Hosoi S, Nakai A, Sakai Y, Abe T, Ishi Y, Kiuchi F, Sano T. Chem. Pharm. Bull. 1991; 39: 1365
- 15s Sano T, Toda J, Kashiwaba N, Ohshima T, Tsuda Y. Chem. Pharm. Bull. 1987; 35: 479
- 15t Ito K, Suzuki F, Haruna M. J. Chem. Soc., Chem. Commun. 1978; 733
- 15u Andreev IA, Ratmanova NK, Novoselov AM, Belov DS, Seregina IF, Kurkin AV. Chem. Eur. J. 2016; 22: 7262
- 15v Paladino M, Zaifman J, Ciufolini MA. Org. Lett. 2015; 17: 3422
- 15w Mostowicz D, Dygas M, Kaluza Z. J. Org. Chem. 2015; 80: 1957
- 15x Kalaitzakis D, Montagnon T, Antonatou E, Vassilikogiannakis G. Org. Lett. 2013; 15: 3714
- 16a Ogawa S, Iida N, Tokunaga E, Shiro M, Shibata N. Chem. Eur. J. 2010; 16: 7090
- 16b Juma B, Adeel M, Villinger A, Reinke H, Spannenberg A, Fischer C, Langer P. Adv. Synth. Catal. 2009; 351: 1073
- 16c Tietze LF, Tolle N, Kratzert D, Stalke D. Org. Lett. 2009; 11: 5230
- 16d Zhang F, Simpkins NS, Blake A. Org. Biomol. Chem. 2009; 7: 1963
- 16e Padwa A, Wang Q. J. Org. Chem. 2006; 71: 7391
- 16f Wang Q, Padwa A. Org. Lett. 2006; 8: 601
- 16g Gao S, Tu YQ, Hu X, Wang S, Hua R, Jiang Y, Zhao Y, Fan X, Zhang S. Org. Lett. 2006; 8: 2373
- 16h El Bialy SA. A, Braun H, Tietze LF. Angew. Chem. Int. Ed. 2004; 43: 5391
- 16i Padwa A, Lee HI, Rashatasakhon P, Rose M. J. Org. Chem. 2004; 69: 8209
- 16j Lee HI, Cassidy MP, Rashatasakhon P, Padwa A. Org. Lett. 2003; 5: 5067
- 16k Chikaoka S, Toyao A, Ogasawara M, Tamura O, Ishibashi H. J. Org. Chem. 2003; 68: 312
- 16l Padwa A, Hennig R, Kappe CO, Reger TS. J. Org. Chem. 1998; 63: 1144
- 16m Tsuda Y, Hosoi S, Katagiri N, Kaneko C, Sano T. Heterocycles 1992; 33: 497
- 16n Rigby JH, Qabar M. J. Am. Chem. Soc. 1991; 113: 8975
- 16o Tsuda Y, Hosoi S, Nakai A, Ohshima T, Sakai Y, Kiuchi F. Chem. Commun. 1984; 1216
- 16p Sano T, Toda J. Heterocycles 1982; 18: 229
- 16q Mondon A, Nestler H. J. Chem. Ber. 1979; 112: 1329
- 16r Haruna M, Ito K. Chem. Commun. 1976; 345
- 16s Mondon A, Nestler HJ. Angew. Chem. Int. Ed. 1964; 3: 588
- 17 L’Homme C, Ménard MA, Canesi S. J. Org. Chem. 2014; 79: 8481
- 18a Nahm S, Weinreb SM. Tetrahedron Lett. 1981; 22: 3815
- 18b Huang PQ, Zheng X, Deng X.-M. Tetrahedron Lett. 2001; 42: 9039
- 19 Luche JL. J. Am. Chem. Soc. 1978; 100: 2226
- 20 Sabot C, Commare B, Duceppe MA, Nahi S, Guérard KC, Canesi S. Synlett 2008; 3226
- 21 Sabot C, Guérad KC, Canesi S. Chem. Commun. 2009; 2941
- 22 Guérard KC, Sabot C, Racicot L, Canesi S. J. Org. Chem. 2009; 74: 2039
- 23 Jacquemot G, Canesi S. J. Org. Chem. 2012; 77: 7588
- 24 Griffith WP, Ley SV, Whitcombe GP, White AD. J. Chem. Soc., Chem. Commun. 1987; 21: 1625
- 25a Fittig R. Justus Liebigs Ann. Chem. 1860; 114: 54
- 25b Wagner G. J. Russ. Chem. Soc. 1899; 31: 690
- 25c Meerwein H. Justus Liebigs Ann. Chem. 1914; 405: 129
- 25d Nametkin SS. Justus Liebigs Ann. Chem. 1923; 432: 207
- 25e Olah GA. Acc. Chem. Res. 1976; 9: 41
- 25f Hanson JR. Comp. Org. Synth. 1991; 3: 705
- 26 Guérard KC, Chapelle C, Giroux MA, Sabot C, Beaulieu MA, Achache N, Canesi S. Org. Lett. 2009; 11: 4756
- 27 Guérard KC, Guérinot A, Bouchard-Aubin C, Ménard M.-A, Lepage M, Beaulieu MA, Canesi S. J. Org. Chem. 2012; 77: 2121
- 28a Hesse M. Indolalkaloide in Tabellen - Ergänzungswerk . Springer; Berlin: 1968: 77
- 28b Ban Y, Ohnuma T, Seki K, Oishi T. Tetrahedron Lett. 1975; 16: 727
- 28c Honma Y, Ohnuma T, Ban Y. Heterocycles 1976; 5: 47
- 28d Yoshido K, Sakuma Y, Ban Y. Heterocycles 1987; 25: 47
- 28e Overman LE, Robertson GM, Robichaud AJ. J. Am. Chem. Soc. 1991; 113: 2598
- 28f Campbell EL, Zuhl AM, Liu CM, Boger DL. J. Am. Chem. Soc. 2010; 132: 3009
- 28g Brown KS, Budzikiewicz H, Djerassi C. Tetrahedron Lett. 1963; 4: 1731
- 28h Walser A, Djerassi C. Helv. Chim. Acta 1965; 48: 391
- 29 Stork G, Dolfini JE. J. Am. Chem. Soc. 1963; 85: 2872
- 30a Hirst GC, Johnson TO, Overman LE. J. Am. Chem. Soc. 1993; 115: 2992
- 30b MacMillan DW. C, Overman LE. J. Am. Chem. Soc. 1995; 117: 10391
- 30c Overman LE, Pennington LD. Can. J. Chem. 2000; 78: 732
- 30d Lebsack AD, Overman LE, Valentkovitch RJ. J. Am. Chem. Soc. 2001; 123: 4851
- 30e Overman LE, Velthuisen EJ. J. Org. Chem. 2006; 1581
- 30f Armstrong A, Bhonoah Y, Shanahan SE. J. Org. Chem. 2007; 72: 8019
- 30g Overman LE, Pennington LD. J. Org. Chem. 2003; 68: 7143
- 30h Lavigne RM. A, Riou M, Girardin M, Morency L, Barriault L. Org. Lett. 2005; 7: 5921
- 30i Tang JM, Bhunia S, Sohel SM. A, Lin M.-Y, Liao HY, Datta S, Das A, Liu RS. J. Am. Chem. Soc. 2007; 129: 15677
- 30j Korotchenko VN. Gagné M. R. J. Org. Chem. 2007; 72: 4877
- 30k Kirsch SF, Binder JT, Crone B, Duschek A, Haug TT, Liebert C, Menz H. Angew. Chem. Int. Ed. 2007; 46: 2310
- 30l Baskar B, Bae HJ, An SE, Cheong JY, Rhee YH, Duschek A, Kirsch SF. Org. Lett. 2008; 10: 2605
- 30m Huang X, Zhang L. J. Am. Chem. Soc. 2007; 129: 6398
- 31a Beaulieu MA, Sabot C, Achache N, Guérard KC, Canesi S. Chem. Eur. J. 2010; 16: 11224
- 31b Beaulieu MA, Guérard KC, Maertens G, Sabot C, Canesi S. J. Org. Chem. 2011; 76: 9460
- 32 Wang J, Soisson SM, Young K, Shoop W, Kodali S, Galgoci A, Painter R, Parthasarathy G, Tang YS, Cummings R, Ha S, Dorso K, Motyl M, Jayasuriya H, Ondeyka J, Herath K, Zhang CW, Hernandez L, Allocco J, Basilio A, Tormo JR, Genilloud O, Vicente F, Pelaez F, Colwell L, Lee SH, Michael B, Felcetto T, Gill C, Silver LL, Hermes JD, Bartizal K, Barrett J, Schmatz D, Becker JW, Cully D, Singh SB. Nature 2006; 441: 358
- 33 Nicolaou KC, Li A, Edmonds DJ, Tria GS, Ellery SP. J. Am. Chem. Soc. 2009; 116: 16905
- 34 Andrez JA, Giroux MA, Lucien J, Canesi S. Org. Lett. 2010; 12: 4368
- 35 Desjardins S, Andrez JA, Canesi S. Org. Lett. 2011; 13: 3406
- 36a Johnson WS, DuBois GE. J. Am. Chem. Soc. 1976; 98: 1038
- 36b Gravestock MB, Johnson WS, McCarry BE, Ratcliffe BE. J. Am. Chem. Soc. 1978; 100: 4274
- 37a Desjardins S, Maertens G, Canesi S. Org. Lett. 2014; 16: 4928
- 37b Maertens G, Desjardins S, Canesi S. Org. Biomol. Chem. 2016; 14: 6744
- 38a Dalton DR. The Alkaloids: The Fundamental Chemistry, A Biogenetic Approach . In Studies in Organic Chemistry . Vol. 7. Gassman PG. Marcel Dekker; New York: 1979: 57
- 38b Martin SF. In The Alkaloids . Vol. 30. Brossi A. Academic Press; New York: 1987: 251
- 38c Ghosal S, Saini KS, Razdan S. Phytochemistry 1985; 24: 2141
- 38d Mineshita T, Yamaguchi K, Takeda K, Kotera K. Annu. Rep. Shionogi Res. Lab. 1956; 6: 119
- 38e Chattopadhyay U, Chaudhuri L, Das S, Kumar Y, Ghosal S. Pharmazie 1984; 39: 855
- 38f De Leo P, Dalessandro G, De Santis A, Arrigoni O. Plant Cell Physiol. 1973; 14: 487
- 39a Gorbunova GM, Sheichenko VI, Tolkachev ON. Khim. Prir. Soedin. 1984; 800
- 39b Tokhtabaeva GM, Sheichenko GM, Yartseva IV, Tolkachev ON. Khim. Prir. Soedin. 1987; 23: 727
- 40a Biechy A, Hachisu S, Quiclet-Sire B, Ricard L, Zard SZ. Angew. Chem. Int. Ed. 2008; 47: 1436
- 40b Biechy A, Hachisu S, Quiclet-Sire B, Ricard L, Zard SZ. Tetrahedron 2009; 65: 6730
- 41 Beaulieu MA, Ottenwaelder X, Canesi S. Chem. Eur. J. 2014; 20: 7581
- 42a Wipf P, Kim Y. Tetrahedron Lett. 1992; 33: 5457
- 42b Wipf P, Kim Y, Goldstein D. J. Am. Chem. Soc. 1995; 117: 11106
- 42c Wipf P, Li W. J. Org. Chem. 1999; 64: 4576
- 42d Wipf P, Mareska DA. Tetrahedron Lett. 2000; 41: 4723
- 42e Methot JL, Wipf P. Org. Lett. 2000; 2: 4213
- 43a Boto A, Hernandez R, Suarez E. J. Org. Chem. 2000; 65: 4930
- 43b Boto A, Hernandez R, Leon Y, Suarez E. J. Org. Chem. 2001; 66: 7796
- 44a Pelletier PJ, Caventou JB. Ann. Chim. Phys. 1818; 8: 323
- 44b Pelletier PJ, Caventou JB. Ann. Chim. Phys. 1819; 10: 142
- 45 Woodward RB, Cava MP, Ollis WD, Hunger A, Daeniker HU, Schenker K. J. Am. Chem. Soc. 1954; 76: 4749
- 46 Jacquemot G, Maertens G, Canesi S. Chem. Eur. J. 2015; 21: 7713
- 47a Rawal VH, Iwasa S. J. Org. Chem. 1994; 59: 2685
- 47b Prelog V, Battegay JW. I, Taylor WI. Helv. Chim. Acta 1948; 31: 2244
- 48 Wipf P, Methot JL. Org. Lett. 2000; 2: 4213
- 49 Tits M, Tavernier D, Angenot L. Phytochemistry 1980; 19: 1531
- 50 Boonsombat J, Zhang H, Chughtai M, Hartung J, Padwa A. J. Org. Chem. 2008; 73: 3539
- 51 Maertens G. Canesi S. Fleming I. Chem. Eur. J. 2016; 22: 7090
- 52 Fleming I. In Organocopper Reagents: A Practical Approach . Taylor RJ. K. Oxford University Press; Oxford: 1994: 257-292
- 53 Trost BM. Angew. Chem. Int. Ed. 1995; 34: 259
- 54 Baran PS, Maimone TJ, Richter JM. Nature 2007; 446: 404
- 55a Levy AA, Rains HC, Smiles S. J. Chem. Soc. 1931; 3264
- 55b Truce WE, Kreider EM, Brand WW. Org. React. 1970; 18: 99
- 56a Chen J, Chen JJ, Yao X, Gao K. Org. Biomol. Chem. 2011; 9: 5334
- 56b Jing P, Yang Z, Zhao C, Zheng H, Fang B, Xie X, She X. Chem. Eur. J. 2012; 18: 6729
- 56c Kuehne ME, Hafter R. J. Org. Chem. 1978; 43: 3702
- 57 Coulibali S, Godou T, Canesi S. Org. Lett. 2016; 18: 4348
- 58 Kan T, Fukuyama T. Chem. Commun. 2004; 353
- 59 Evans DA, Bartroli J, Shih TL. J. Am. Chem. Soc. 1981; 103: 2127
- 60 Coulibali S, Deruer E, Godin E, Canesi S. Org. Lett. 2017; 19: 1188
For reviews or books see:
For publications see: