7126-47-8Relevant academic research and scientific papers
Substrate Controlled Regioselective Bromination of Acylated Pyrroles Using Tetrabutylammonium Tribromide (TBABr3)
Gao, Shuang,Bethel, Travis K.,Kakeshpour, Tayeb,Hubbell, Grace E.,Jackson, James E.,Tepe, Jetze J.
, p. 9250 - 9255 (2018/07/15)
Electrophilic bromination of pyrroles bearing carbonyl substituents at C-2 typically results in a mixture of the 4- and 5-brominated species, generally favoring the 4-position. Herein, we describe a substrate-controlled regioselective bromination in which
N,N-Dimethyl-1H-pyrrole-2-carboxamide
Linden, Anthony,Wright, Anthony D.,Koenig, Gabriele M.
, p. 744 - 747 (2007/10/02)
The low-temperature X-ray crystal structure of N,N-dimethyl-1H-pyrrole-2-carboxamide, C7H10N2O, was determined.The molecular geometry indicates that the carbonyl ? system interacts preferentially with the lone-pair electrons of the amide N atom rather than with the ? system of the pyrrole ring.Intermolecular hydrogen bonds link the molecules into centrosymmetric dimers.
3-Substituted-5,6,7,8-tetrahydropyrrolo[1,2-a]-pyridine-and 6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]-azepine carboxylic acid derivatives useful as blood platelet aggregation inhibitors
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, (2008/06/13)
Novel 3-substituted-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylic acid and 3-substituted-6,7,8,9-tetrahydro[1,2-a]azepine-9-carboxylic acid compounds represented by the formula STR1 and the pharmaceutically acceptable, non-toxic esters and salts t
