Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Laurence G. Cool"'
Publikováno v:
Magnetic Resonance in Chemistry. 59:23-33
The connectivity, conformation, tautomeric form, and dynamics of a new depsidone (perisalazinic acid) were characterized using one-bond 13 C13 C NMR scalar couplings (1 JCC ) obtained from the INADEQUATE experiment. Characterization of perisalazin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c723f947d358f9b1823701d8dbf3903a
https://doi.org/10.1002/mrc.5077
https://doi.org/10.1002/mrc.5077
Publikováno v:
Natural product research.
Individuals of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b4a156ebc33d977958c02bb0ceea505f
https://pubmed.ncbi.nlm.nih.gov/35156862
https://pubmed.ncbi.nlm.nih.gov/35156862
Individuals of Usnea fulvoreagens (Parmeliaceae, lichenised Ascomycota), a shrubby corticolous species that is widespread in Europe, East Asia and North America, produce medullary lichen acids in several distinct chemotypic patterns. One such chemoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8725c276bd2f4c6d6b46027a0bf5d4c4
Publikováno v:
Magnetic Resonance in Chemistry. 59:5-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85e59f8902c1c95be6628e0c11f0d3b5
https://doi.org/10.1002/mrc.5080
https://doi.org/10.1002/mrc.5080
Publikováno v:
The Journal of organic chemistry. 83(10)
A carbocation cyclization/rearrangement mechanism for the biosynthesis of isothapsadiene and β-isothapsenol is shown to be energetically viable on the basis of density functional theory (DFT) calculations. In addition, for both isothapsadiene and β
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1543aa0a220c94253a1838d4c46f80f
https://pubmed.ncbi.nlm.nih.gov/29684282
https://pubmed.ncbi.nlm.nih.gov/29684282
Autor:
Laurence G. Cool
Publikováno v:
Phytochemistry. 66:249-260
Ten sesquiterpenes, many with unusual carbon skeletons, were identified in foliage of Cupressus macrocarpa. These are (-)-10-epi-beta-acoradiene; ent-widdra-2,4(14)-diene; (E)-iso-gamma-bisabolene, i.e., (4E)-4-(1,5-dimethylhex-5-enylidene)-1-methylc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee84f242a068283307f48c710b1b82a
https://doi.org/10.1016/j.phytochem.2004.11.002
https://doi.org/10.1016/j.phytochem.2004.11.002
Publikováno v:
Phytochemistry Letters. 4:158-160
The root essential oil of Ligusticum grayi Coult. & Rose (Apiaceae) was found to contain three volatile non-terpenoid hydrocarbons: the known C11 compound viridene, whose structure is hereby corrected to 1-[(2Z)-pent-2-en-1-yl]cyclohexa-1,3-diene; an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ee0b322075fab358ab3e921f243cda9
https://doi.org/10.1016/j.phytol.2011.02.006
https://doi.org/10.1016/j.phytol.2011.02.006
Autor:
Laurence G. Cool
Publikováno v:
Phytochemistry. 58:969-972
One new ent-daucadiene and enantiomers of four previously reported daucadienes or acoradienes were identified in foliage of the hybrid cypress species xCupressocyparis leylandii. The major compound is (+)-dauca-5,8-diene; minor congeners are (-)-dauc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::778bfda8aa7e6ee1f127a140cc828eca
https://doi.org/10.1016/s0031-9422(01)00342-9
https://doi.org/10.1016/s0031-9422(01)00342-9
Publikováno v:
Journal of Chemical Ecology. 27:1449-1479
Soldier defense secretions from samples of Reticulitermes collected in California, Nevada, Arizona, New Mexico, and Georgia were characterized and correlated with cuticular hydrocarbon phenotypes. Twenty-seven cuticular hydrocarbon phenotypes have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22b5bebe7b07f73c2b9f11fa9768a50e
https://doi.org/10.1023/a:1010325511844
https://doi.org/10.1023/a:1010325511844
Publikováno v:
Biochemical Systematics and Ecology. 26:899-913
Foliage of trees from five Chinese Cupressus species was analysed for volatile monoterpenoids, sesquiterpenoids and diterpenoids. Multivariate analysis of the terpenoid data indicated that C. gigantea is most distinct, but otherwise no obvious chemot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcb0129ab9d4d9a4b8fffa01b4c4faa0
https://doi.org/10.1016/s0305-1978(98)00037-4
https://doi.org/10.1016/s0305-1978(98)00037-4