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Alkyne derivatives aldehyde trapping

The alternative building scheme C2 + Q was used by Petasis and Hu [89], who reacted various aldehydes and ketones with alkenyltitanocene derivatives 172 to obtain the corresponding allenes 173 in high chemical yields (Scheme 2.54). The reaction probably proceeds via titanocene vinylidene complexes, which can also be trapped with alkynes and isocyanides to afford allenylketene imines [90],... [Pg.81]

Dehydrobromination of bromotrifluoropropene affords the more expensive trifluoropropyne [237], which was metallated in situ and trapped with an aldehyde in the TIT group s [238]synthesis of 2,6-dideoxy-6,6,6-trifluorosugars (Eq. 77). Allylic alcohols derived from adducts of this type have been transformed into trifluoromethyl lactones via [3,3] -Claisen rearrangements and subsequent iodolactonisation [239]. Relatively weak bases such as hydroxide anion can be used to perform the dehydrobromination and when the alkyne is generated in the presence of nucleophilic species, addition usually follows. Trifluoromethyl enol ethers were prepared (stereoselectively) in this way (Eq. 78) the key intermediate is presumably a transient vinyl carbanion which protonates before defluorination can occur [240]. Palladium(II)-catalysed alkenylation or aryla-tion then proceeds [241]. [Pg.162]

The reaction between lithio TMS-diazomethane and carbonyl compounds, which generates alkyUdenecarbenes, has been studied further. Aliphatic ketones give cyclopentene derivatives, while aldehydes and aryl alkyl ketones give alkynes. The diazoalkene intermediates from aliphatic ketones can be trapped with diisopropylamine, producing... [Pg.1675]

P-Ketophosphonates are valuable intermediates in the realm of Homer-Emmons alkenation methodology. Acyclic variants are difficult to obtain from enol phosphates due to competing alkyne and allene formation. One solution utilized the dianion derived from a-bromo ketones and trapping with diethyl phosphorochloridate however, only moderate yields of P-keto phosphonates were reported. The most efficient procedure utilizes the anion derived from dialkyl methylphosphonate, addition to an aldehyde, followed by oxidation (eq 8). ... [Pg.145]


See other pages where Alkyne derivatives aldehyde trapping is mentioned: [Pg.100]    [Pg.16]    [Pg.100]    [Pg.100]    [Pg.100]    [Pg.314]    [Pg.375]    [Pg.146]    [Pg.88]    [Pg.63]    [Pg.112]    [Pg.184]   
See also in sourсe #XX -- [ Pg.1364 , Pg.1365 ]




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