Some scientific research about tert-Butyl (3-aminobicyclo[1.1.1]pentan-1-yl)carbamate

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 1638767-25-5. SDS of cas: 1638767-25-5.

Chemistry is an experimental science, SDS of cas: 1638767-25-5, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1638767-25-5, Name is tert-Butyl (3-aminobicyclo[1.1.1]pentan-1-yl)carbamate, molecular formula is C10H18N2O2, belongs to amides-buliding-blocks compound. In a document, author is Gressies, Steffen.

An interrupted Schmidt rearrangement/Hosomi-Sakurai reaction of N-tosyl and S-substituted vinyl azides is reported. With BF3 center dot Et2O as a Lewis acid promoter, the denitrogenative fragmentation of vinyl azides facilitates the generation of the N/S-stabilized carbocations, which further undergo nucleophilic addition by allyl/propargylsilanes for C-C bond formation. As a result, a variety of homoallylic/allenylic amines can be afforded in good yields under mild reaction conditions with well-defined functional-group tolerance.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 1638767-25-5. SDS of cas: 1638767-25-5.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics