107393-03-3Relevant articles and documents
Prek, Benjamin,Po?kaj, Marta,Kantlehner, Willi,Stanovnik, Branko
, p. 501 - 513 (2018)
Biosynthesis inspired Diels-Alder route to pyridines: synthesis of the 2,3-dithiazolylpyridine core of the thiopeptide antibiotics.
Moody, Christopher J,Hughes, Rachael A,Thompson, Stewart P,Alcaraz, Lilian
, p. 1760 - 1761 (2007/10/03)
Reaction of serine derived 1-alkoxy-2-azadienes with dehydroalanine derived dienophiles results in Diels-Alder reaction and aromatisation to give 2,3,6-trisubstituted pyridines, thereby establishing the viability of the proposed biosynthetic route to the
α-PHENYLISOCINCHOMERONIC AND 4-AZAFLUORENONE 3-CARBOXYLIC ACIDS
Prostakov, N. S.,Sakha Shibu Rani,Mikhailova, N. M.,Sergeeva, N. D.
, p. 529 - 532 (2007/10/02)
3,6-Dimethyl-2-phenylpyridine, obtained on phenylation of 2,5-lutidine, has been used in the synthesis of α-phenylisocinchomeronic acid, derivatives of it, and also for the preparation of 4-azafluorenone 3-carboxylic acid.It was established that 4-hydroxy-3,6-dimethyl-2-phenylpyridine was formed on phenylation of 2,5-lutidine.