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Tandem intramolecular/intermolecular metathesi

Enyne systems are also capable of impressive multiple RRM transformations. For the first such example see Ref. [119]. The reaction of a ruthenium alkyli-dene with an alkyne produces a new vinyl alkylidene, which can participate in further intramolecular or intermolecular metathesis reactions to form fused ring systems. This has led Grubbs to designate alkynes in such systems as relays . In a noteworthy example, Zuercher et al. [ 120] constructed the four fused rings of the steroid backbone 68 in one efficient step using tandem enyne re-... [Pg.113]

A simultaneous intermolecular/intramolecular enyne metathesis process using diynes (e.g., 267) and allylsilane 268 afforded conjugated triene derivatives (e.g., 270). Gyclopropanation was observed as a side-reaction in the tandem enyne metathesis RCM of diene-yne 271. ... [Pg.188]

Grubbs has reported a similar tandem olefin metathesis-carbonyl olelination process for the preparation of cyclic olefins [31]. In this case, treatment of a keto-olefin with the molybdenum alkylidene 1 at 20°C generates an intermediate alkylidene complex. Under these conditions, competing intermolecular olelination does not occur. However, intramolecular carbonyl olelination of the initially formed alkylidene complex can occur and this results in the formation of a cyclic olefin. This tandem sequence is illustrated by the transformation of keto-olefins... [Pg.102]


See other pages where Tandem intramolecular/intermolecular metathesi is mentioned: [Pg.270]    [Pg.270]    [Pg.186]    [Pg.13]    [Pg.485]    [Pg.250]    [Pg.408]    [Pg.3]    [Pg.738]   
See also in sourсe #XX -- [ Pg.270 ]




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