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Kang Hyun Jung

Kang Hyun Jung. Introduction. Leucascandrolide A ( 1 , Scheme 1) was isolated in 1996 from the calcareous sponge Leucascandra caveolata , collected off the east coast of New Caledonia, by Pietra and co-workers.

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Kang Hyun Jung

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  1. Kang Hyun Jung

  2. Introduction Leucascandrolide A (1, Scheme 1) was isolated in 1996 from the calcareous sponge Leucascandra caveolata, collected off the east coast of New Caledonia, by Pietra and co-workers. - This polyoxygenated 18-membered macrolide features two trisubstituted tetrahydropyran rings, one of which has an unusual oxazole-bearing unsaturated side chain. - Biological studies revealed potent cytotoxic activity against a range of cancer cell lines (IC50¼0.05 and 0.25 mgmL1 against KB oral epidermoid carcinoma and P388 leukemia cell lines, respectively), as well as pronounced antifungal activity.

  3. Retro-Synthetic Analysis

  4. Preparation of Advanced Intermediate 18

  5. Jacobson Asymmetric Hetero Diels-Alder Reaction [1]

  6. HgII-Mediated Hydration of Alkyne [2] - Alkynes are less basic than alkenes, Hg(OAc)2 (Hg+2 is a Lewis acid) is added to ensure complete reaction

  7. 1,5-Anti Stereoindution in the Boron-Mediated Aldol Reaction[3] Org. Lett.,4, 4325-4328, 2002

  8. 1,3-Anti Reduction of β-Hydroxy Ketone[4] J. Am. Chem. Soc., 110, 11, 3560-3578, 1988

  9. Selective Iodine(III)/TEMPO-Mediated Oxidation [5] J. Org. Chem., 62, 6974-6977, 1997

  10. Elaboration to the Macrocyclic Core 24

  11. DIBAL Reduction and in situ Acetylation [6] J. Org. Chem., 61, 8317-8320, 1996

  12. 1,3-Asymmetric redution [7]

  13. Mistunobu Macrolactonization (Esterification)[8] Synthesis, 1, 1981

  14. Preparation of the Oxazole-bearing Side Chain 3

  15. α-Alkylation of Hydrazone and Alkyl halide [9]

  16. Sonogashira Coupling of Functionalized Trifloyl Oxazole [10] Org. Lett.,4, 2485-2488, 2002

  17. Completion of the Total Synthesis of Leucascandrolide A

  18. Lindlar Hydrogenation [11]

  19. Conclusion • In summary, we have completed a highly stereocontrolled synthesis • of the potent cytotoxic macrolide leucascandrolide A, proceeding in • 23 steps from 8 (longest linear sequence) and 5.3% overall yield. Key • features include a Jacobsen asymmetric hetero Diels-Alder reaction • to configure the right-hand tetrahydropyran ring, a 1,5-anti aldol • coupling, control over the C17 hydroxy center, and two sequential • Mitsunobu reactions, to close the 18-membered macrolactone and • append the oxazole-bearing side chain, respectively.

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