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Volumn 10, Issue 6, 2008, Pages 1223-1226

An approach to the core skeleton of lancifodilactone F

Author keywords

[No Author keywords available]

Indexed keywords

LANCIFODILACTONE F; TRITERPENE;

EID: 45549103450     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol800111j     Document Type: Article
Times cited : (56)

References (60)
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    • Isolation of lancifodilactones
    • Isolation of lancifodilactones:
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    • (c) Xiao, W.-L.; Li, R.-T.; Li, S.-H.; Li, X.-L.; Sun, H.-D.; Zheng, Y.-T.; Wang, R.-R.; Lu, Y.; Wang, C.; Zheng, Q.-T. Org. Lett. 2005, 7, 1263-1266; correction: Org. Lett. 2006, 8, 801.
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    • (d) Xiao, W.-L.; Zhu, H.-J.; Shen, Y.-H.; Li, R.-T.; Li, S.-H.; Sun, H.-D.; Zheng, Y.-T.; Wang, R-R.; Lu, Y.; Wang, C.; Zheng, Q.-T. Org. Lett. 2005, 7, 2145-2148; correction: Org. Lett. 2006, 8, 801.
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    • Isolation of micrandilactones
    • Isolation of micrandilactones:
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    • (a) Li, R.-T.; Zhao, Q.-S.; Li, S.-H.; Han, Q.-B.; Sun, H.-D.; Lu, Y.; Zhang, L.-L.; Zheng, Q.-T. Org. Lett. 2003, 5, 1023-1026; correction: Org. Lett. 2006, 8, 801.
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    • (c) Li, R.-T.; Xiao, W.-L.; Shen, Y.-H.; Zhao, Q.-S.; Sun, H.-D. Chem.-Eur. J. 2005, 11, 2989-2996; correction: Chem.-Eur. J. 2005, 11, 6763-6765. Synthetic studies:
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    • Isolation of hendridilactones: Li, R.; Shen, Y.; Xiang, W.; Sun, H.-D. Eur. J. Org. Chem. 2004, 807-811.
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    • Isolation of sphenadilactones: Xiao, W.-L.; Pu, J.-X.; Chang, Y.; Li, X.-L.; Huang, S.-X.; Yang, L.-M.; Li, L.-M.; Lu, Y.; Zheng, Y.-T.; Li, R.-T.; Zheng, Q.-T.; Sun, H.-D. Org. Lett. 2006, 8, 1475-1478; correction: Org. Lett. 2006, 8, 4669.
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    • Isolation of rubriflordilactones: Xiao, W.-L.; Yang, L.-M.; Gong, N.-B.; Wu, L.; Wang, R.-R.; Pu, J.-X.; Li, X.-L.; Huang, S.-X.; Zheng, Y.-T.; Li, R.-T.; Lu, Y.; Zheng, Q.-T.; Sun, H.-D. Org. Lett. 2006, 8, 991-994.
    • Isolation of rubriflordilactones: Xiao, W.-L.; Yang, L.-M.; Gong, N.-B.; Wu, L.; Wang, R.-R.; Pu, J.-X.; Li, X.-L.; Huang, S.-X.; Zheng, Y.-T.; Li, R.-T.; Lu, Y.; Zheng, Q.-T.; Sun, H.-D. Org. Lett. 2006, 8, 991-994.
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    • Cyathane diterpenoids also bear a 5, 6, 7-tricylic core skeleton. For examples of their synthesis, see:
    • Cyathane diterpenoids also bear a 5, 6, 7-tricylic core skeleton. For examples of their synthesis, see:
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    • There has been no report of synthetic studies on buxapentalactone. For isolation of selected Buxus triterpenoids, see:
    • There has been no report of synthetic studies on buxapentalactone. For isolation of selected Buxus triterpenoids, see:
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    • The crystallographic data of 1 published by Sun and co-workers (CCDC-254747) supports the (9R)-configuration instead. However, the anisotropic displacement parameters for most atoms are not acceptable, including 15 of them being non-positive definite. The published data do not contain suitable information for reinterpretation.
    • The crystallographic data of 1 published by Sun and co-workers (CCDC-254747) supports the (9R)-configuration instead. However, the anisotropic displacement parameters for most atoms are not acceptable, including 15 of them being non-positive definite. The published data do not contain suitable information for reinterpretation.
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    • Ellis-Davies, G. C. R.; Gilbert, A.; Heath, P.; Lane, J. C; Warrington, J. V.; Westover, D. L. J. Chem. Soc, Perkin Trans. 2 1984, 1833-1841. There is one exception reported by De Keukeleire and He. Irradiation of a 3-benzyloxymethylcyclopentene derivative at 254 nm in cyclohexane-ethyl acetate (5:1) gave the meta-photocycloaddition product in 42% yield:
    • (d) Ellis-Davies, G. C. R.; Gilbert, A.; Heath, P.; Lane, J. C; Warrington, J. V.; Westover, D. L. J. Chem. Soc, Perkin Trans. 2 1984, 1833-1841. There is one exception reported by De Keukeleire and He. Irradiation of a 3-benzyloxymethyl)cyclopentene derivative at 254 nm in cyclohexane-ethyl acetate (5:1) gave the meta-photocycloaddition product in 42% yield:
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    • Wender and DeLong have found that photolysis of an oxygen-bridged arene-olefin system with Hanovia medium-pressure mercury lamp through Vycor glass in cyclohexane for 2 h provided the desired meta-photocycloaddition products in 68% yield at 60% conversion based on recovered starting material. Prolong irradiation led to product decomposition. DeLong, M. Ph.D. Thesis, Stanford University, 1992
    • Wender and DeLong have found that photolysis of an oxygen-bridged arene-olefin system with Hanovia medium-pressure mercury lamp through Vycor glass in cyclohexane for 2 h provided the desired meta-photocycloaddition products in 68% yield at 60% conversion based on recovered starting material. Prolong irradiation led to product decomposition. DeLong, M. Ph.D. Thesis, Stanford University, 1992.
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    • Review: Mehta, Venkateswaranb R. V . Tetrahedron 2000, 56. 1399-1422.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.