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Multistrategic retrosynthetic analysis

The application of multistrategic retrosynthetic analysis to the target perhydro-histrionicotoxin is outlined in Section 6.3 of Part One. [Pg.136]

The multistrategic retrosynthetic analysis of retigeranic acid, which led to the synthesis outlined below, has been described in Section 6.6 of Part One. [Pg.215]

Forskolin is an activator of the enzyme adenylate cyclase which has therapeutic utility. Outlined below are stereocontrolled routes to racemic and natural chiral forms of forskolin derived by multistrategic retrosynthetic analysis. [Pg.248]

See other pages where Multistrategic retrosynthetic analysis is mentioned: [Pg.81]    [Pg.81]    [Pg.81]    [Pg.83]    [Pg.83]    [Pg.83]    [Pg.84]    [Pg.86]    [Pg.89]    [Pg.440]    [Pg.3]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.92]    [Pg.92]    [Pg.92]    [Pg.93]    [Pg.95]    [Pg.98]    [Pg.81]    [Pg.81]   
See also in sourсe #XX -- [ Pg.15 , Pg.91 ]



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Analysis retrosynthetic

Multistrategic Retrosynthetic Analysis of Gibberellic Acid

Multistrategic Retrosynthetic Analysis of Ginkgolide

Multistrategic Retrosynthetic Analysis of Porantherine

Multistrategic Retrosynthetic Analysis of Retigeranic Acid

Retrosynthetic

Strategy multistrategic retrosynthetic analysis

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