DOI QR코드

DOI QR Code

Synthesis of (-)-Pyrenophorol

  • Oh, Hong-Se (Department of Chemistry, Chungbuk National University) ;
  • Kang, Han-Young (Department of Chemistry, Chungbuk National University)
  • 투고 : 2011.03.02
  • 심사 : 2011.03.29
  • 발행 : 2011.08.20

초록

키워드

참고문헌

  1. Kis, Z.; Furger, P.; Sigg, H. P. Experientia 1969, 25, 123-124. https://doi.org/10.1007/BF01899073
  2. Grove, J. F. J. Chem. Soc., C. 1971, 2261-2263. https://doi.org/10.1039/j39710002261
  3. Nozoe, S.; Hirai, K.; Tsuda, K.; Ishibashi, K.; Shirasaka, M. Tetrahedron Lett. 1965, 6, 4675-4677. https://doi.org/10.1016/S0040-4039(01)84033-8
  4. Noda, A.; Aoyagi, S.; Machinaga, N.; Kibayashi, C. Tetrahedron Lett. 1994, 35, 8237-8240. https://doi.org/10.1016/0040-4039(94)88291-6
  5. MacMillan, J.; Simpson, T. J. J. Chem. Soc. Perkin I 1973, 1487-1493. https://doi.org/10.1039/p19730001487
  6. Krohn, K.; Farooq, U.; Florke, U.; Schulz, B.; Draeger, S.; Pescitelli, G.; Salvadori, P.; Antus, S.; Kurtan, T. Eur. J. Org. Chem. 2007, 3206-3211.
  7. Zhang, W.; Krohn, K.; Egold, H.; Draeger, S.; Schulz, B. Eur. J. Org. Chem. 2008, 4320-4328.
  8. Machinaga, N.; Kibayashi, C. Tetrahedron Lett. 1993, 34, 841-844. https://doi.org/10.1016/0040-4039(93)89027-N
  9. Dommerholt, F. J.; Thijs, L.; Zwanenburg, B. Tetrahedron Lett. 1991, 32, 1495-1498. https://doi.org/10.1016/0040-4039(91)80367-F
  10. Dommerholt, F. J.; Thijs, L.; Zwanenburg, B. Tetrahedron Lett. 1991, 32, 1499-1502. https://doi.org/10.1016/0040-4039(91)80368-G
  11. Yadav, J. S.; Subba Reddy, U. V.; Subba Reddy, B. V. Tetrahedron Lett. 2009, 50, 5984-5986. https://doi.org/10.1016/j.tetlet.2009.07.047
  12. Lee, D.-M.; Kang, H.-Y. Bull. Korean Chem. Soc. 2008, 29, 1671-1672. https://doi.org/10.5012/bkcs.2008.29.9.1671
  13. Csuk, R.; Prell, E.; Reißmann, S. Tetrahedron 2008, 64, 9417-9422. https://doi.org/10.1016/j.tet.2008.07.089
  14. Sharma, G. V. M.; Mallesham, S.; Mouli, C. C. Tetrahedron: Asymmetry 2009, 20, 2513-2529. https://doi.org/10.1016/j.tetasy.2009.10.030

피인용 문헌

  1. A Chemoenzymatic Synthesis of Hept-6-ene-2,5-diol Stereomers: Application to Asymmetric Synthesis of Decarestrictine L, Pyrenophorol, and Stagonolide E vol.79, pp.17, 2014, https://doi.org/10.1021/jo5012575
  2. Stereoselective total synthesis of (−)-(5S,8R,13S,16R)-pyrenophorol vol.146, pp.8, 2015, https://doi.org/10.1007/s00706-014-1406-3
  3. Asymmetric Hydroformylation-Initiated Tandem Sequences for Syntheses of (+)-Patulolide C, (−)-Pyrenophorol, (+)-Decarestrictine L, and (+)-Prelog Djerassi Lactone vol.80, pp.1, 2015, https://doi.org/10.1021/jo502301k
  4. Stereoselective total synthesis of (−)-pyrenophorol pp.1336-9075, 2018, https://doi.org/10.1007/s11696-017-0331-4
  5. An alternative stereoselective total synthesis of (-)-pyrenophorol pp.1478-6427, 2018, https://doi.org/10.1080/14786419.2018.1499636
  6. Asymmetric Catalytic Alkynylation of Acetaldehyde: Application to the Synthesis of (+)‐Tetrahydropyrenophorol vol.124, pp.27, 2011, https://doi.org/10.1002/ange.201203035
  7. Asymmetric Catalytic Alkynylation of Acetaldehyde: Application to the Synthesis of (+)‐Tetrahydropyrenophorol vol.51, pp.27, 2011, https://doi.org/10.1002/anie.201203035
  8. Stereoselective total synthesis of C2-symmetric natural products pyrenophorol and its derivatives vol.34, pp.15, 2020, https://doi.org/10.1080/14786419.2019.1577843