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Mackay, M. F., Sadek, M., Culvenor, C. C. J. (1984) Crispatine monohydrate, C16H23NO5.H2O, a pyrrolizidine alkaloid. Acta Crystallographica Section C Crystal Structure Communications, 40 (3) 470-472 doi:10.1107/s0108270184004534

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Reference TypeJournal (article/letter/editorial)
TitleCrispatine monohydrate, C16H23NO5.H2O, a pyrrolizidine alkaloid
JournalActa Crystallographica Section C Crystal Structure Communications
AuthorsMackay, M. F.Author
Sadek, M.Author
Culvenor, C. C. J.Author
Year1984 (March 15)Volume40
Issue3
PublisherInternational Union of Crystallography (IUCr)
DOIdoi:10.1107/s0108270184004534Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID223029Long-form Identifiermindat:1:5:223029:4
GUID0
Full ReferenceMackay, M. F., Sadek, M., Culvenor, C. C. J. (1984) Crispatine monohydrate, C16H23NO5.H2O, a pyrrolizidine alkaloid. Acta Crystallographica Section C Crystal Structure Communications, 40 (3) 470-472 doi:10.1107/s0108270184004534
Plain TextMackay, M. F., Sadek, M., Culvenor, C. C. J. (1984) Crispatine monohydrate, C16H23NO5.H2O, a pyrrolizidine alkaloid. Acta Crystallographica Section C Crystal Structure Communications, 40 (3) 470-472 doi:10.1107/s0108270184004534
In(1984, March) Acta Crystallographica Section C Crystal Structure Communications Vol. 40 (3) International Union of Crystallography (IUCr)

See Also

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Mackay, M. F., Sadek, M., Culvenor, C. C. J., Smith, L. W. (1984) Dehydromonocrotaline, C16H21NO6: active metabolite of the pyrrolizidine alkaloid monocrotaline. Acta Crystallographica Section C Crystal Structure Communications, 40 (3) 473-476 doi:10.1107/s0108270184004546
Mackay, M. F., Sadek, M., Culvenor, C. C. J. (1984) α- and β-epoxides from monocrotaline, a pyrrolizidine alkaloid: 1,2-dihydro-1α,2α-epoxymonocrotaline, C16H23NO7, and 1,2-dihydro-1β,2β-epoxymonocrotaline monohydrate, C16H23NO7.H2O. Acta Crystallographica Section C Crystal Structure Communications, 40 (12) 2064-2068 doi:10.1107/s0108270184010647
Mackay, M. F., Mitrprachachon, P., Culvenor, C. C. J. (1985) Hygrophylline, C18H27NO6: a pyrrolizidine alkaloid. Acta Crystallographica Section C Crystal Structure Communications, 41 (3) 395-397 doi:10.1107/s0108270185004036
Mackay, M. F., Culvenor, C. C. J. (1983) Grantaline, C18H25NO6, a pyrrolizidine alkaloid. Acta Crystallographica Section C Crystal Structure Communications, 39 (9) 1227-1230 doi:10.1107/s0108270183008021
Mackay, M. F., Sadek, M., Culvenor, C. C. J., Smith, L. W. (1983) Dehydrosenecionine, C18H23NO5: active metabolite of the pyrrolizidine alkaloid senecionine. Acta Crystallographica Section C Crystal Structure Communications, 39 (9) 1230-1233 doi:10.1107/s0108270183008033
Mackay, M. F., Sadek, M., Culvenor, C. C. J. (1984) Ethanol–water solvates of anacrotine and madurensine, C18H25NO6.1/2C2H6O.1/2H2O. Isomeric pyrrolizidine alkaloids. Acta Crystallographica Section C Crystal Structure Communications, 40 (6) 1073-1077 doi:10.1107/s0108270184006831
Mackay, M. F., Sadek, M., Culvenor, C. C. J. (1983) Lycopsamine and intermedine, C15H25NO5: diastereoisomeric pyrrolizidine alkaloids. Acta Crystallographica Section C Crystal Structure Communications, 39 (6) 785-788 doi:10.1107/s0108270183006320
Gable, R. W., Mackay, M. F., Culvenor, C. C. J. (1988) Echinatine, C15H25NO5, a pyrrolizidine alkaloid. Acta Crystallographica Section C Crystal Structure Communications, 44 (8) 1478-1481 doi:10.1107/s0108270188004792
Mackay, M. F., Culvenor, C. C. J. (1982) Structure of senecionine, a pyrrolizidine alkaloid. Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 38 (10) 2754-2758 doi:10.1107/s056774088200987x
Hay, D. G., Mackay, M. F., Culvenor, C. C. J. (1982) The structure of lasiocarpine: a pyrrolizidine alkaloid. Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 38 (1) 155-159 doi:10.1107/s0567740882002271
Mackay, M. F., Mitrprachachon, P., Oliver, P. J., Culvenor, C. C. J. (1985) Supinine, C15H25NO4, and heleurine, C16H27NO4, pyrrolizidine alkaloids. Acta Crystallographica Section C Crystal Structure Communications, 41 (5) 722-725 doi:10.1107/s0108270185005261
 
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