Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Aristolane

Ji N-Y, Li X-M, Ding L-P, Wang B-G (2007) Aristolane Sesquiterpenes and Highly Brominated Indoles from the Marine Red Alga Laurencia similis (Rhodomelaceae). Helv Chim Acta 90 385... [Pg.440]

Addition of vinylmagnesium bromide to tricyclononenone 10, prepared in three steps from cycloheptatriene, results in the formation of a 4 1 epimeric mixture of allylic alcohol 11, which undergoes oxy-Cope rearrangement to give tricyclic enone 12, the ring system of the aristolane sesquiterpene10715. [Pg.379]

Ji NY, Li XM, Ding LP, Wang BG (2007) Aristolane sesquiterpenes and highly brominated indoles from the marine red alga Laurencia similis Rhodomelaceae). Helv Chim Acta 90 385-391... [Pg.41]

Tanitsu MA, Takaya Y, Akasaka M, Niwa M, Oshima Y (2002) Guaiane- and aristolane-type sesquiterpenoids of Nardostachys chinensis roots. Phytochemistry 59 845-849... [Pg.3064]

Two bisabolane and aristolane sesquiterpenes substituted with unusual nitrile and thioqranate groups have recently been characterized in Axinyssa isabela from Mexico (Figure... [Pg.977]

Do, M.N. and Erickson, KL. (1983) Aristolane sesquiterpenoid from seapen Scytalium splendent. ]. Org. Chem., 48,4410-4413. [Pg.1374]

See other pages where Aristolane is mentioned: [Pg.106]    [Pg.75]    [Pg.338]    [Pg.106]    [Pg.46]    [Pg.121]    [Pg.122]    [Pg.461]    [Pg.120]    [Pg.120]    [Pg.405]    [Pg.902]    [Pg.912]    [Pg.925]    [Pg.926]    [Pg.87]    [Pg.33]    [Pg.920]    [Pg.751]    [Pg.743]    [Pg.1]    [Pg.15]    [Pg.15]    [Pg.15]    [Pg.268]    [Pg.224]    [Pg.343]    [Pg.1804]    [Pg.1807]    [Pg.1878]   
See also in sourсe #XX -- [ Pg.46 ]

See also in sourсe #XX -- [ Pg.15 ]



SEARCH



Aristolanes

© 2024 chempedia.info