94252-16-1Relevant academic research and scientific papers
Organocatalytic Enantioselective Michael-Addition of Malonic Acid Half-Thioesters to β-Nitroolefins: From Mimicry of Polyketide Synthases to Scalable Synthesis of γ-Amino Acids
Bae, Han Yong,Some, Surajit,Lee, Jae Heon,Kim, Ju-Young,Song, Myoung Jong,Lee, Sungyul,Zhang, Yong Jian,Song, Choong Eui
supporting information; experimental part, p. 3196 - 3202 (2012/02/01)
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs) to a variety of nitroolefins, affording the optically active γ-amino acid precursors, were developed by employing the Cinchona-based squaramides (up to >
