1346240-94-5Relevant articles and documents
Aerobic synthesis of pyrroles and dihydropyrroles from imines: Palladium(II)-catalyzed intramolecular C-H dehydrogenative cyclization
Shi, Zhuangzhi,Suri, Mamta,Glorius, Frank
supporting information, p. 4892 - 4896 (2013/06/04)
sp3ectacularly mild! An efficient PdII-catalyzed intramolecular dehydrogenative cyclization of imines affords (dihydro)pyrrole products using molecular oxygen as the sole oxidant. This mild formal sp 3-C-H functionalization allows rapid and atom-economical assembly of (dihydro)pyrrole rings from inexpensive and readily available allylamines and ketones. A broad range of functional groups are tolerated. Copyright
A simple and efficient protocol to 1,2,4-substituted pyrroles via a sonogashira coupling-acid-catalyzed cyclization
Zhu, Da,Zhao, Jie,Wei, Yuxiu,Zhou, Hongwei
supporting information; experimental part, p. 2185 - 2186 (2011/10/09)
A facile and efficient protocol for the synthesis of 1,2,4-substituted pyrrole derivatives was developed. As a result of the ready availability of materials and the simple operation, this type of reaction should have potential utility in organic synthesis. Georg Thieme Verlag Stuttgart · New York.