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Propargyltitanium reagents

P-Acetylenic alcohols (11, 378). The propargyltitanium reagent derived from 1-trimethylsilyl-3-(tetrahydropyranyloxy)propyne (1) reacts with crotonaldehydes to afford the P-acetylenic alcohol 2 with high stereoselectivity. This alcohol was used in a stcr-eocontrolled synthesis of the natural antibiotic ( )-asperlin (6). [Pg.353]

In organic synthesis, propargyltitanium(rV) complexes are unique among the organometallic reagents in that they perform efficient addition of either alkynic or allenic residues to carbonyl compounds. [Pg.165]

Since this topic will be covered extensively in Part 1 Volume 2, only the main references concerning their preparation and their more significant synthetic applications are recalled at this point. - Hetero-substituted propargyltitanium(IV) reagents are also very useful in the synthesis of natural products. [Pg.165]


See other pages where Propargyltitanium reagents is mentioned: [Pg.336]    [Pg.52]    [Pg.336]    [Pg.92]    [Pg.336]    [Pg.52]    [Pg.336]    [Pg.92]    [Pg.165]    [Pg.165]   
See also in sourсe #XX -- [ Pg.378 ]




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Propargyltitanium

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