Synthesis 2024; 56(10): 1608-1618
DOI: 10.1055/a-2250-8050
paper

Nicholas Reactions of Pentadiynyl–Co2(CO)6 Cations. Synthesis of Antimalarial Hinokiresinol Analogues

,
Funding was provided by the Natural Sciences and Engineering Research Council (NSERC Canada) Discovery Grant program (RGPIN-2022-04761).


Abstract

Penta-1,4-diyn-3-ol–Co2(CO)6 complexes undergo Lewis acid mediated Nicholas reactions with high selectivity at the C-3 site, to give skipped (1,4-)diyne complexes. The compatible nucleophiles have a wide range of reactivity. The methodology has been applied to the synthesis of both (E)- and (Z)-isomers of a hinokiresinol and nyasol analogue, the (E)-isomer of which is known to have elevated antiplasmodial and antimalarial activity.

Supporting Information



Publication History

Received: 18 September 2023

Accepted after revision: 22 January 2024

Accepted Manuscript online:
22 January 2024

Article published online:
14 February 2024

© 2024. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

    • 1a Green JR, Nicholas KM. Org. React. 2020; 103: 931
    • 1b Kann N. Curr. Org. Chem. 2012; 16: 322
    • 1c Shea JM. In Name Reactions for Homologations, Part 1. Li JJ. Wiley; Hoboken: 2009: 284-298
    • 1d Diaz DD, Betancort JM, Martín VS. Synlett 2007; 343
    • 1e Teobald BJ. Tetrahedron 2002; 58: 4133
    • 1f Green JR. Curr. Org. Chem. 2001; 5: 809
    • 1g Caffyn AJ. M, Nicholas KM. In Comprehensive Organometallic Chemistry II, Vol. 12, Chap. 7.1. Abel EW, Stone FG. A, Wilkinson G. Pergamon; Oxford: 1995
    • 2a Padmanabhan S, Nicholas KM. Tetrahedron Lett. 1982; 23: 2555
    • 2b DiMartino J, Green JR. Tetrahedron 2006; 62: 1402
    • 2c de la Torre MC, Asenjo M, Ramírez-Lopez P, Sierra MA. Eur. J. Org. Chem. 2015; 1054
    • 2d Mahmood A, Ngenzi R, Penner PM, Green JR. Synlett 2016; 27: 1245
    • 3a Shiyuba S, Isobe M. Tetrahedron 1998; 54: 6677
    • 3b Lobo F, Gomez AM, Miranda S, Lopez JC. Chem. Eur. J. 2014; 20: 10492
    • 3c Kolodziej I, Green JR. Org. Biomol. Chem. 2015; 13: 10852
    • 4a Liu T, Liu Y, Guo W. Org. Chem. Front. 2022; 9: 3312
    • 4b Liu Y, Liu T, Yan B, Wei K, Guo W. Adv. Synth. Catal. 2022; 364: 916
    • 4c Mahrwald R, Quint S. Tetrahedron 2000; 56: 7463
    • 5a Mayr H, Heilmann W. Tetrahedron 1986; 42: 6657
    • 5b Giner X, Trillo P, Nájera C. J. Organomet. Chem. 2011; 696: 357
    • 5c Gu H, Sun X, Wang Y, Wu YH, Wu P. RSC Adv. 2018; 8: 1737

      Pd:
    • 6a Kimura M, Horino Y, Mukai R, Tanaka S, Tamaru Y. J. Am. Chem. Soc. 2001; 123: 10401
    • 6b Christie SD. R, Warrington AD, Lunniss CJ. Synthesis 2009; 148

    • Ru:
    • 6c Gruber S, Zaitsev AB, Wӧrle M, Pregosin PS. Organometallics 2008; 27: 3796

    • Fe:
    • 6d Donaldson WA, Chaudhury S. Eur. J. Org. Chem. 2009; 3831
    • 6e Knölker HJ. In Organometallics in Synthesis . Schlosser M. Wiley; Hoboken: 2013: 545-776
    • 8a Schwier T, Rubin M, Gevorgyan V. Org. Lett. 2004; 6: 1999
    • 8b Mahrwald R, Quint A. Tetrahedron Lett. 2001; 42: 1655
    • 8c Teng G, Mo S, Pan J, Wu N, Wanf H, Pan Y. Synthesis 2016; 48: 455
    • 9a Melikyan GG, Anker B. Organometallics 2015; 34: 4194
    • 9b Melikyan GG, Davis R, Anker B, Meron D, Duncan K. Organometallics 2016; 35: 4060
  • 10 For an alternative Nicholas reaction based approach to skipped diynes, see: Guo R, Gibe R, Green JR. Can. J. Chem. 2004; 82: 366
  • 11 Skytte DM, Nielsen SF, Chen M, Zhai L, Olsen CE, Christensen SB. J. Med. Chem. 2006; 49: 436
    • 12a Nguyen T.-H.-T, Pham H.-V.-T, Pham N.-K.-T, Quach N.-D.-P, Pudhom K, Hansen PE, Nguyen K.-P.-P. Bioorg. Med. Chem. Lett. 2015; 25: 2366
    • 12b Li Y.-F, Hu L.-H, Lou F.-C, Hong J.-R, Li J, Shen Q. J. Asian Nat. Prod. Res. 2005; 7: 43
  • 13 Mukai C, Suzuki K, Nagami K, Hanaoka M. J. Chem. Soc., Perkin Trans. 1 1992; 141
  • 14 Eisler S, Chahal N, McDonald R, Tykwinski RR. Chem. Eur. J. 2003; 9: 2542
  • 15 St Onge B, Green JR. Synlett 2017; 28: 2923
    • 16a Mayr H, Kempf B, Ofial AR. Acc. Chem. Res. 2003; 36: 66
    • 16b Tokuyasu T, Mayr H. Eur. J. Org. Chem. 2004; 2791
  • 17 Review: Marciniec B, Maciejewski H, Pietraszuk C, Pawluć P. In Hydrosilylation. A Comprehensive Review on Recent Advances . Marciniec B. Springer; Dordrecht: 2009: 53-86
  • 18 Magre M, Szewczyk M, Rueping M. Org. Lett. 2020; 22: 1594
    • 19a Yu J, Gaunt MJ, Spencer JB. J. Org. Chem. 2002; 67: 4627
    • 19b Schwarz M, Graminski GF, Waters RM. J. Org. Chem. 1986; 51: 260
    • 19c Clark DA, Clark JR, Diver ST. Org. Lett. 2008; 10: 2055
  • 20 Kim IS, Dong GR, Jung YH. J. Org. Chem. 2007; 72: 5424
  • 21 Muresan M. M.Sc. Thesis 2022
  • 22 Still WC, Kahn M, Mitra A. J. Org. Chem. 1978; 43: 2923