Merritt, Eleanor A.; Bagley, Mark C. published the artcile< Convergent synthesis of the central heterocyclic domain of micrococcin P1>, Application In Synthesis of 6136-93-2, the main research area is thiazolylpyridine micrococcin P1 core preparation; aminopentadienone Bohlmann Rahtz intramol cyclodehydration; keto ester ammonium acetate amination microwave.
The heterocyclic domain I of micrococcin P1 was prepared from N-Boc-(2S,3R)-threonine in 15 steps and 9% overall yield utilizing a microwave-assisted enamine formation in mono- or multimode instruments, Bohlmann-Rahtz pyridine synthesis to form the 2,3,6-trisubstituted pyridine motif, and two-directional elaboration of the 3- and 6-thiazole substituents.
Synlett published new progress about Amination. 6136-93-2 belongs to class nitriles-buliding-blocks, and the molecular formula is C6H11NO2, Application In Synthesis of 6136-93-2.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts