119216-44-3Relevant academic research and scientific papers
A New and Efficient Strategy for Non-stabilized Azomethine Ylide via Photoinduced Electron Transfer (PET) Initiated Sequential Double Desilylation
Pandey, Ganesh,Lakshmaiah, G.,Kumaraswamy, G.
, p. 1313 - 1314 (1992)
A practical approach for generating non-stabilized azomethine ylide by PTE initiation is generated.
Sequential two-electron oxidation of α,α′-disilylmethylamines to generate non-stabilized azomethine ylide: An ideal approach for the construction of substituted and fused pyrrolidine ring systems
Pandey, Ganesh,Lakshmaiah,Gadre, Smita R.
, p. 91 - 98 (2007/10/03)
α,α′-Di(trimethylsilylmethyl)amines undergo sequential double desilylation processes, by two-electron oxidation initiated either by photoinduced electron transfer (PET) or Ag(I)F, to produce non-stabilized azomethine ylides efficiently which upon trapping with appropriate dipolarophiles give the corresponding pyrrolidines. Application of this strategy to cyclic analogue for the rapid construction of biologically important 1-azabicyclo[m,3.0]alkane framework is discussed.
SYNTHESIS OF 3-PYRROLINES VIA A -ANNULATION STRATEGY
Padwa, Albert,Norman, Bryan H.
, p. 3041 - 3044 (2007/10/02)
The reaction of amines with 2,3-diphenylsulfonyl-1,3-butadiene produces 3-pyrrolines which are readily oxidized to 3-phenylsulfonyl pyrroles.
