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brevifoliol/taxus wallichiana
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A brevifoliol analogue from the Himalyan yew Taxus wallichiana.
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The needles of Taxus wallichiana gave a new brevifoliol derivative whose structure was established by spectral data.
Minor taxoids from Taxus wallichiana.
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The needles of Taxus wallichiana afforded a new analogue of taxinine M [1a] and two derivatives of brevifoliol [2a, 3a]. The conformation of 3a was investigated by nmr spectroscopy with the aid of variable-temperature experiments and in situ reactions.
Wallifoliol, a taxol congener with a novel carbon skeleton, from Himalayan Taxus wallichiana.
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A new taxoid, wallifoliol [3], has been isolated, along with five known taxoids (taxol, cephalomannine, 10-deacetylbaccatin III, brevifoliol, 2-acetoxy brevifoliol = taxchinin A) from extracts of the needles of Himalayan Taxus wallichiana. The structure of wallifoliol has been assigned primarily
Brevifoliol and its Analogs: A New Class of Antitubercular Agents
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Brevifoliol is an abeo-taxane isolated from the Taxus wallichiana needles, eighteen semi-synthetic esters derivatives of brevifoliol were prepared by Steglich esterification and screened for their anti-tubercular potential against Mycobacterium tuberculosis H37Ra avirulent strain. The 3-[chloro (7)]
Analysis of taxol and major taxoids in Himalayan yew, Taxus wallichiana.
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A reversed-phase column liquid chromatography method for the analysis of taxol, 10-deacetylbaccatin III, baccatin IV, 1-hydroxybaccatin I, 2-acetoxybrevifoliol, brevifoliol, 2'-deacetoxydecinnamoyltaxinine J and 2'-deacetoxytaxinine J in yew needles has been developed using a Nova-Pak Phenyl column
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