21485-45-0Relevant academic research and scientific papers
Sterically-controlled regioselective para-substitutions of aniline
Dyer, Philip W.,Fawcett, John,Griffith, Gerald A.,Hanton, Martin J.,Olivier, Celine,Patterson, Adam R.,Suhard, Samuel
, p. 3835 - 3837 (2005)
Introduction of statically demanding 1-isopropyl-2-methyl-propyl or triisopropylsilyl groups at the nitrogen of aniline allows high-yielding regioselective para-substitution to be achieved using a lithiation/substitution sequence. The Royal Society of Che
Aminodiphenylphosphanes: Isotope-induced chemical shifts 1Δ14/15N(31P), coupling constants 1J(31P,15N), and chemical shifts δ15N and δ31P
Contreras, Rosalinda,Grevy, Jean Michel,Garcia-Hernandez, Zureima,Goeizado-Rodriguez, Marisol,Wrackmeyer, Bernd
, p. 542 - 550 (2007/10/03)
A series of aminodiphenylphosphanes 1 [Ph2P-N(H)tBu (a), -NEt2 (b), -NiPr2 (c)], 2 [Ph2P-NHPh (a), -NH-2-pyridine (b), -NH-3-pyridine (c), -NH-4-pyridine (d), NH-pyrimidine (e), NH-2,6-Me2-C6/su
