147369-09-3Relevant academic research and scientific papers
Microbial Baeyer-Villiger oxidation applied to the synthesis of the N-protected (1R,5R)-Geisman-Waiss lactone
Luna, Amparo,Gutierrez, Maria-Concepcion,Furstoss, Roland,Alphand, Veronique
, p. 2521 - 2524 (2007/10/03)
Using whole cell Baeyer-Villiger biooxidation as a key step and depending on the choice of the biocatalyst {E. coli TOP10[pQR239] or Acinetobacter TD63}, the synthesis of nearly enantiopure N-protected (1R,5R)-(-)-Geisman-Waiss lactone (92% ee) or its (1R
Cycloaddition Reaction of Cyclic Enecarbamates and Enamides With Ketenes. A Short and Efficient Synthesis of the Geissman-Waiss Lactone.
Faria, Antonio R. de,Matos, Carlos Roberto R.,Correia, Carlos Roque D.
, p. 27 - 30 (2007/10/02)
The synthesis of several 2-aza-bicycloheptan-6-ones has been achieved in a regiospecific manner through a cycloaddition reaction between five-membered cyclic enecarbamates and enamides and free ketenes.The synthetic potential of this new meth
