164801-58-5Relevant academic research and scientific papers
Palladium(II)-catalyzed cycloisomerization of functionalized 1,5-hexadienes
Nelson, Bjoern,Hiller, Wolf,Pollex, Annett,Hiersemann, Martin
, p. 4438 - 4441 (2011/10/08)
Scope and limitations of the Pd(II)-catalyzed cycloisomerization of functionalized 1,5-hexadienes have been studied. In situ NMR experiments indicate a challenging competition between various reaction pathways. A careful balance between substrate structur
Silylated cyclohexadienes in radical chain hydrosilylations
Amrein, Stephan,Studer, Armido
, p. 3559 - 3574 (2007/10/03)
A new method for the mild radical hydrosilylation of alkenes and alkynes is described. Silylated cyclohexadienes that can be readily prepared on large scale are used as radical hydrosilylating reagents. Nonactivated alkenes and alkynes are hydrosilylated in high yields. The reaction can be combined with C-C bond formation, as demonstrated for the preparation of silylated cycloalkanes from the corresponding dienes. Furthermore, radical hydrosilylations in combination with β-fragmentation reactions for the synthesis of allylsilanes and hydrosilylations of aldehydes and ketones providing protected alcohols can be readily performed by this strategy.
Sequential Homoaldolization-Cuprate Rearrangement in a Stereoselective Synthesis of Stannyl Dienes: Application to the Synthesis of the Western C10-C15 Subunit of (+/-)-Tylosin Aglycon
Menez, Patrick Le,Fargeas, Valerie,Berque, Isabelle,Poisson, Jacques,Ardisson, Janick,et al.
, p. 3592 - 3599 (2007/10/02)
A stereospecific synthesis of stannyl diene 5, corresponding to the C10-C15 fragment of (+/-)-tylosin aglycon 2, was reported.Silyl carbamate 16, submitted to the Hoppe homoaldolization conditions with propanal, gave the anti aldol product 17 in 89percent yield.Further treatment including oxidation of the silyl group led to lactone 21.The corresponding dihydrofuran 23 was then transformed into vinylstannane 25, via an efficient Kocienski rearrangement.An iodide exchange was performed on 25 and followed by a Stille coupling reaction with tributylstannyl acetylide.Stannyl cupration of the resulting silylated enyne 27 led in 44percent yield to a 1:1 mixture of the desired (E,E)-stannyl diene 5b and the unexpected (E,Z) isomer 29.The same reaction performed on desilylated enyne 28 delivered in 85percent yield the pure (E,E)-stannyl diene 5.
