Awesome Chemistry Experiments For tert-Butyl 4-formylpiperidine-1-carboxylate

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A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Safety of tert-Butyl 4-formylpiperidine-1-carboxylate, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 137076-22-3, Name is tert-Butyl 4-formylpiperidine-1-carboxylate, molecular formula is C11H19NO3. In a Article, authors is Gao, Shang，once mentioned of 137076-22-3

Cu-catalyzed stereoselective synthesis of (E)-delta-silyl-anti-homoallylic alcohols from 1,3-dienylsilane was developed. Mechanistic studies revealed that the borocupration of dienylsilane proceeded through a 1,2-addition pathway to give an allylcopper intermediate with Cu distal to the silyl group. However, the subsequent aldehyde allylation proceeded via Curtin-Hammett control to give (E)-delta-silyl-anti-homoallylic alcohols with high diastereoselectivities. This method was applied to the synthesis of the C1-9 fragment of a polyketide natural product, mycinolide IV.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 137076-22-3, help many people in the next few years.Safety of tert-Butyl 4-formylpiperidine-1-carboxylate

Reference：
Piperidine – Wikipedia,
Piperidine | C5H16399N – PubChem