RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000083.xml
Synlett 2017; 28(01): 1-11
DOI: 10.1055/s-0036-1588372
DOI: 10.1055/s-0036-1588372
account
Pardon the Interruption: A Modification of Fischer’s Venerable Reaction for the Synthesis of Heterocycles and Natural Products
Weitere Informationen
Publikationsverlauf
Received: 17. November 2016
Accepted: 21. November 2016
Publikationsdatum:
08. Dezember 2016 (online)
‡ These authors contributed equally.
Abstract
This account provides an overview of our laboratory’s studies of an unusual variant of the Fischer indolization reaction. We describe the discovery of the so-called ‘interrupted Fischer indolization’ and the development of the reaction from a methodological standpoint. In addition, our efforts to evaluate and apply this methodology in the context of akuammiline alkaloid total synthesis are discussed.
1 Introduction
2 Interrupted Fischer Indolization Methodology
3 Applications in Akuammiline Alkaloid Total Synthesis
4 Concluding Thoughts
-
References
- 1 See: http://garg.chem.ucla.edu/.
- 2 Garg NK, Sarpong R, Stoltz BM. J. Am. Chem. Soc. 2002; 124: 13179
-
3a Garg NK, Caspi DD, Stoltz BM. J. Am. Chem. Soc. 2004; 126: 9552
- 3b Garg NK, Caspi DD, Stoltz BM. J. Am. Chem. Soc. 2005; 127: 5970
-
4a Garg NK, Hiebert S, Overman LE. Angew. Chem. Int. Ed. 2006; 45: 2912
-
4b Becker MH, Chua P, Downham R, Douglas CJ, Garg NK, Hiebert S, Jaroch S, Matsuoka RT, Middleton JA, Ng FW, Overman LE. J. Am. Chem. Soc. 2007; 129: 11987
- 5a Sunazuka T, Yoshida K, Kojima N, Shirahata T, Hirose T, Handa M, Yamamoto D, Harigaya Y, Kuwajima I, Omura S. Tetrahedron Lett. 2005; 46: 1459
- 5b Chiou W.-H, Kao C.-L, Tsai J.-C, Chang Y.-M. Chem. Commun. 2013; 49: 8232
- 5c Matsuura T, Overman LE, Poon DJ. J. Am. Chem. Soc. 1998; 120: 6500
- 5d Shishido K, Shitara E, Komatsu H, Hiroya K, Fukumoto K, Kametani T. J. Org. Chem. 1986; 51: 3007
- 5e Takano S, Moriya M, Ogasawara K. J. Org. Chem. 1991; 56: 5982
- 5f Zhou B, Hou W, Yang Y, Feng H, Li Y. Org. Lett. 2014; 16: 1322
- 5g De S, Das MK, Bhunia S, Bisai A. Org. Lett. 2015; 17: 5922
- 5h Zhang TY, Zhang H. Tetrahedron Lett. 2002; 43: 1363
- 5i Clark AJ, Jones K. Tetrahedron 1992; 48: 6875
- 5j Kulkarni MG, Dhondge AP, Borhade AS, Gaikwad DD, Chavhan SW, Shaikh YB, Nigdale VB, Desai MP, Birhade DR, Shinde MP. Eur. J. Org. Chem. 2009; 3875
- 5k Chen J.-Q, Wei Y.-L, Xu G.-Q, Liang Y.-M, Xu P.-F. Chem. Commun. 2016; 52: 6455
- 5l Shao Z, Zhang H. Youji Huaxue 2005; 25: 282
- 5m Morales-Ríos MS, Santos-Sánchez NF, Joseph-Nathan P. J. Nat. Prod. 2002; 65: 136
- 5n Tanaka K, Taniguchi T, Ogasawara K. Tetrahedron Lett. 2001; 42: 1049
- 6a Ruiz-Sanchis P, Savina SA, Albericio F, Alvarez M. Chem. Eur. J. 2011; 17: 1388
- 6b ElAzab AS, Taniguchi T, Ogasawara K. Org. Lett. 2000; 2: 2757
- 6c Ishibashi H, Kobayashi T, Machida N, Tamura O. Tetrahedron 2000; 56: 1469
- 6d Node M, Hao X.-J, Nishide K, Fuki K. Chem. Pharm. Bull. 1996; 44: 715
- 6e Yu QS, Lu BY. Heterocycles 1994; 39: 519
- 6f Morales-Ríos MS, Santos-Sánchez NF, Fragoso-Vázquez MJ, Alagille D, Villagómez-Ibarra JR, Joseph-Nathan P. Tetrahedron 2003; 59: 2843
- 6g Horne S, Taylor N, Collins S, Rodrigo R. J. Chem. Soc., Perkin Trans. 1 1991; 3047
- 6h Yu Q, Liu C, Brzostowska M, Chrisey L, Brossi A, Greig NH, Atack JR, Soncrant TT, Rapoport SI, Radunz H. Helv. Chim. Acta 1991; 74: 761
- 6i Luo Y, Yu Q, Chrisey L, Brossi A. Heterocycles 1990; 31: 283
- 6j Shishido K, Azuma T, Shibuya M. Tetrahedron Lett. 1990; 31: 219
- 6k Tadamasa O. Tetrahedron Lett. 1971; 12: 4391
- 6l Dale FJ, Robinson B. J. Pharm. Pharmacol. 1970; 22: 889
- 6m Longmore RB, Robinson B. J. Chem. Soc., Chem. Commun. 1967; 2184
- 6n Trost BM, Zhang Y. J. Am. Chem. Soc. 2006; 128: 4590
- 7a Wu Y, Wang F, Song H, Qin Y. Helv. Chim. Acta 2011; 94: 1496
- 7b Badiola E, Fiser B, Gomez-Bengoa E, Mielgo A, Olaizola I, Urruzuno I, Garcia JM, Odriozola JM, Razkin J, Oiarbide M, Palomo C. J. Am. Chem. Soc. 2014; 136: 17869
- 7c Pandey G, Khamrai J, Mishra A. Org. Lett. 2015; 17: 952
- 8 For select studies pertaining to 4 and its isomers, see: Büeschleb M, Dorich S, Hanessian S, Tao D, Schenthal KB, Overman LE. Angew. Chem. Int. Ed. 2016; 55: 4156
- 9a Li J, Jeong S, Esser L, Harran PG. Angew. Chem. Int. Ed. 2001; 40: 4765
- 9b Li J, Burgett AW. G, Esser L, Amezcua C, Harran PG. Angew. Chem. Int. Ed. 2001; 40: 4770
- 9c Nicolaou KC, Bella M, Chen DY.-K, Huang X, Ling T, Snyder SA. Angew. Chem. Int. Ed. 2002; 41: 3495
- 9d Nicolaou KC, Rao PB, Hao J, Reddy MV, Rassias G, Huang X, Chen DY.-K, Snyder SA. Angew. Chem. Int. Ed. 2003; 42: 1753
- 9e Burgett AW. G, Li Q, Wei Q, Harran PG. Angew. Chem. Int. Ed. 2003; 42: 4961
- 9f Knowles RR, Carpenter J, Blakey SB, Kayano A, Mangion IK, Sinz CJ, MacMillan DW. C. Chem. Sci. 2011; 2: 308
- 10a Trost BM, Osipov M. Chem. Eur. J. 2015; 21: 16318
- 10b May JA, Zeidan RK, Stoltz BM. Tetrahedron Lett. 2003; 44: 1203
- 11a Subramaniam G, Hiraku O, Hayashi M, Koyano T, Komiyama K, Kam T.-S. J. Nat. Prod. 2007; 70: 1783
- 11b Subramaniam G, Kam T.-S. Helv. Chim. Acta 2008; 91: 930
- 12 Kam T.-S, Tan S.-J, Ng S.-W, Komiyama K. Org. Lett. 2008; 10: 3749
- 13a Garg NK, Woodroofe CC, Lacenere CJ, Quake SR, Stoltz BM. Chem. Commun. 2005; 4551
- 13b Lacenere CJ, Garg NK, Stoltz BM, Quake SR. Nucleosides, Nucleotides Nucleic Acids 2005; 25: 9
- 14 For the use of cyanine dyes in DNA sequencing, see: Braslavsky I, Hebert B, Kartalov E, Quake SR. Proc. Natl. Acad. Sci. U.S.A. 2003; 100: 3960
- 15 The approximate cost of Cy3 is $286.00 for enough dye to label 1 mg of protein (GE Healthcare).
- 16 Li Q, Tan J, Peng B.-X. Molecules 1997; 2: 91
- 17a Fischer E, Jourdan F. Ber. 1883; 16: 2241
- 17b Fischer E, Hess O. Ber. 1884; 17: 559
- 18a Campos KR, Woo JC. S, Lee S, Tillyer RD. Org. Lett. 2004; 6: 79
- 18b Brodfuehrer PR, Chen B.-C, Sattelberg TR, Smith PR, Reddy JP, Stark DR, Quinlan SL, Reid JG, Thottathil JK, Wang S. J. Org. Chem. 1997; 62: 9192
- 18c Adachi H, Palaniappan KK, Ivanov AA, Bergman N, Gao Z.-G, Jacobson KA. J. Med. Chem. 2007; 50: 1810
- 19a Boal BW, Schammel AW, Garg NK. Org. Lett. 2009; 11: 3458
- 19b Schammel AW, Boal BW, Zu L, Mesganaw T, Garg NK. Tetrahedron 2010; 66: 4687
- 20a Grandberg II, Zuyanova TI, Afonina NI, Ivanova TA. Dokl. Akad. Nauk SSSR 1967; 176: 583
- 20b Britten AA, Bardsley WG, Hill CM. Tetrahedron 1971; 27: 5631
- 20c Grandberg II, Tokmakov GP. Khim. Geterotsikl. Soedin. 1975; 207
- 20d Rosenmund P, Sadri E. Liebigs Ann. Chem. 1979; 927
- 20e Rosenmund P, Gektidis S, Brill H, Kalbe R. Tetrahedron Lett. 1989; 30: 61
- 20f Takano S, Moriya M, Iwabuchi Y, Ogasawara K. Chem. Lett. 1990; 109
- 20g Takano S, Ogasawara K, Iwabuchi R, Moriya M. JP 03112989 A 19910514, 1991
- 20h Tsuji R, Nakagawa M, Nishida A. Heterocycles 2002; 58: 587
- 20i Nishida A, Ushigome S, Sugimoto A, Arai S. Heterocycles 2005; 66: 181
- 21a Müller S, Webber MJ, List B. J. Am. Chem. Soc. 2011; 133: 18534
- 21b Martínez A, Webber MJ, Müller S, List B. Angew. Chem. Int. Ed. 2013; 52: 9486
- 22 Çelebi-Ölçüm N, Boal BW, Huters AD, Garg NK, Houk KN. J. Am. Chem. Soc. 2011; 133: 5752
- 23 Schammel AW, Chiou G, Garg NK. Org. Lett. 2012; 14: 4556
- 24 Schammel AW, Chiou G, Garg NK. J. Org. Chem. 2012; 77: 725
- 25 Lahiri DK, Chen D, Maloney B, Holloway HW, Yu Q.-S, Utsuki T, Giordano T, Sambamurti K, Greig NH. J. Pharmacol. Exp. Ther. 2007; 320: 396
- 26a Ramírez A, García-Rubio S. Curr. Med. Chem. 2003; 10: 1891
- 26b Eckermann R, Gaich T. Synthesis 2013; 45: 2813
- 26c Smith JM, Moreno J, Boal BW, Garg NK. Angew. Chem. Int. Ed. 2015; 54: 400
- 27 Baliga MS. Chin. J. Integr. Med. 2012; DOI: 10.1007/s11655-011-0947-0.
-
28 The first akuammiline alkaloid total synthesis was reported by Qin in 2009, see: Zhang M, Huang X, Shen L, Qin Y. J. Am. Chem. Soc. 2009; 131: 6013
- 29a Adams GL, Carroll PJ, Smith III AB. J. Am. Chem. Soc. 2012; 134: 4037
- 29b Zi W, Xie W, Ma D. J. Am. Chem. Soc. 2012; 134: 9126
- 29c Adams GL, Carroll PJ, Smith III AB. J. Am. Chem. Soc. 2013; 135: 519
- 29d Horning BD, MacMillan DW. C. J. Am. Chem. Soc. 2013; 135: 6442
- 29e Smith MW, Snyder SA. J. Am. Chem. Soc. 2013; 135: 12964
- 29f Teng M, Zi W, Ma D. Angew. Chem. Int. Ed. 2014; 53: 1814
- 29g Ren W, Wang Q, Zhu J. Angew. Chem. Int. Ed. 2014; 53: 1818
- 29h Ren W, Wang Q, Zhu J. Angew. Chem. Int. Ed. 2016; 55: 3500
- 29i Li Y, Zhu S, Li J, Li A. J. Am. Chem. Soc. 2016; 138: 3982
- 29j Nishiyama D, Ohara A, Chiba H, Kumagai H, Oishi S, Fujii N, Ohno H. Org. Lett. 2016; 18: 1670
- 29k Li G, Xie X, Zu L. Angew. Chem. Int. Ed. 2016; 55: 10483
- 29l Eckermann R, Breunig M, Gaich T. Chem. Commun. 2016; 52: 11363
- 30a Zu L, Boal BW, Garg NK. J. Am. Chem. Soc. 2011; 133: 8877
- 30b Smith JM, Moreno J, Boal BW, Garg NK. J. Am. Chem. Soc. 2014; 136: 4504
- 30c Smith JM, Moreno J, Boal BW, Garg NK. J. Org. Chem. 2015; 80: 8954
- 30d Moreno J, Picazo E, Morrill LA, Smith JM, Garg NK. J. Am. Chem. Soc. 2016; 138: 1162
- 31a Battersby AR, Thompson M, Glüsenkamp K.-H, Tietze L.-F. Chem. Ber. 1981; 114: 3430
- 31b Battersby AR, Westcoltt ND, Glüsenkamp K.-H, Tietze L.-F. Chem. Ber. 1981; 114: 3439
- 31c Scott AI. Acc. Chem. Res. 1970; 3: 151
- 31d Stöckigt J, Barleben L, Panjikar S, Loris EA. Plant Physiol. Biochem. 2008; 46: 340
- 32 Under a variety of interrupted Fischer indolization conditions, substrate 53 underwent facile dehydration to give the corresponding dihydrofuran.
- 33 Although ketone 54 underwent condensation with phenylhydrazine under several interrupted Fischer indolization conditions, no evidence of [3,3]-sigmatropic rearrangement was detected.
- 34a Chatterjee A, Mukherjee B, Ray AB, Das B. Tetrahedron Lett. 1965; 6: 3633
- 34b Kam T.-S, Nyeoh K.-T, Sim K.-M, Yoganathan K. Phytochemistry 1997; 45: 1303
- 34c Cai X.-H, Liu YP, Feng T, Luo X.-D. Chin. J. Nat. Med. 2008; 6: 20
- 35 Hypervalent iodine reagents such as PhI(OAc)2 and periodic acid were ineffective for this transformation.
- 36 VanRheenen V, Kelly RC, Cha DY. Tetrahedron Lett. 1976; 17: 1973
- 37 Burk RM, Roof MB. Tetrahedron Lett. 1993; 34: 395
- 38 For the removal of nosyl groups using a solid-supported thiol reagent, see: Cardullo F, Donati D, Merlo G, Paio A, Salaris M, Taddei M. Synlett 2005; 2996
- 39a Schnoes HK, Biemann K, Mokry J, Kompis I, Chatterjee A, Ganguli G. J. Org. Chem. 1966; 31: 1641
- 39b For the X-ray structure of strictamine, see: Ahmad Y, Fatima K, Atta-ur-Rahman Occolowitz JL, Solheim BA, Clardy J, Garnick RL, Le Quesne PW. J. Am. Chem. Soc. 1977; 99: 1943
- 40a Dolby LJ, Esfandiari Z. J. Org. Chem. 1972; 37: 43
- 40b Dolby LJ, Nelson SJ. J. Org. Chem. 1973; 38: 2882
- 40c Bennasar M.-L, Zulaica E, López M, Bosch J. Tetrahedron Lett. 1988; 29: 2361
- 40d Bennasar M.-L, Zulaica E, Ramírez A, Bosch J. J. Org. Chem. 1996; 61: 1239
- 40e Koike T, Takayama H, Sakai S.-I. Chem. Pharm. Bull. 1991; 39: 1677
- 40f Edwankar RV, Edwankar CR, Namjoshi OA, Deschamps JR, Cook JM. J. Nat. Prod. 2012; 75: 181
- 40g Komatsu Y, Yoshida K, Ueda H, Tokuyama H. Tetrahedron Lett. 2013; 54: 377
- 40h Kawano M, Kiuchi T, Negishi S, Tanaka H, Hoshikawa T, Matsuo J.-I, Ishibashi H. Angew. Chem. Int. Ed. 2013; 52: 906
- 40i Ren W, Tappin N, Wang Q, Zhu J. Synlett 2013; 24: 1941
- 41 For the reductive interrupted Fischer indolization reaction, see: Maligres PE, Houpis I, Rossen K, Molina A, Sager J, Upadhyay V, Wells KM, Reamer RA, Lynch JE, Askin D, Volante RP, Reider PJ, Houghton P. Tetrahedron 1997; 53: 10983
- 42 For the initial isolation of 2(S)-cathafoline, see: Lim S.-H, Low Y.-Y, Sinniah SK, Yong K.-T, Sim K.-S, Kam T.-S. Phytochemistry 2014; 98: 204
- 43 For a review on the nosyl protecting group, see: Kan T, Fukuyama T. Chem. Commun. 2004; 353
- 44a Ueda H, Satoh H, Matsumoto K, Sugimoto K, Fukuyama T, Tokuyama H. Angew. Chem. Int. Ed. 2009; 48: 7600
- 44b Satoh H, Ueda H, Tokuyama H. Tetrahedron 2013; 69: 89
- 44c Krüger S, Gaich T. Angew. Chem. Int. Ed. 2015; 54: 315
- 44d Krüger S, Gaich T. Eur. J. Org. Chem. 2016; 4893
For select studies on physovenine, see:
For a recent review of pyrrolidinoindoline natural product syntheses, see:
See also:
For syntheses of physostigmine since Alvarez’s review (ref. 6a), see:
For a pertinent review, see:
For a seminal and influential study by Stoltz and co-workers, see:
For the classic Fischer indole synthesis, see:
Lactols and hemiaminals had previously been employed in modifications of the Fischer indole synthesis, see:
List’s laboratory ultimately developed an asymmetric Fischer indolization, see:
For other total syntheses of akuammiline alkaloids, see:
For our laboratory’s total syntheses of akuammilines, see:
For the initial isolation of picrinine, see:
For more recent isolation reports, see:
For the initial isolation of strictamine, see:
For previous synthetic studies on strictamine or related methanoquinolizidine akuammilines, see:
For additional examples of the Fischer indolization in late-stage total synthesis of complex alkaloids, see: