29107-26-4Relevant academic research and scientific papers
A mild and efficient bisaldolization of ketones and its application towards spirocyclic 1,3-dioxanes and novel 1,3,5-trioxocanes
Srinivas, Nagarapu,Marrapu, Vijay K.,Bhandari, Kalpana
experimental part, p. 1346 - 1350 (2009/10/19)
Bisaldolization of aryl alkyl ketones as well as cyclic ketones with paraformaldehyde in the presence of a catalytic amount of L-proline and low concentration of aqueous sodium hydroxide has been developed in excellent yields. Further, these bisaldols are
Enantioselective enzymatic desymmetrization of prochiral 1,3-diols and enzymatic resolution of monoprotected 1,3-diols based on α-tetralone and related multifunctional scaffolds
Mahapatra, Tridib,Das, Tapas,Nanda, Samik
experimental part, p. 2497 - 2507 (2009/04/11)
Novel multifunctional chemotypes based on α-tetralone, α-indanone, and chromanone have been synthesized by a chemo-enzymatic approach by applying an enzymatic irreversible transesterification strategy. The scaffolds synthesized can be further elaborated with subsequent enzymatic as well as chemical transformations for the generation of new sets of structurally related organic molecules.
