134927-79-0Relevant academic research and scientific papers
Do reaction conditions affect the stereoselectivity in the staudinger reaction?
Wang, Yikai,Liang, Yong,Jiao, Lei,Du, Da-Ming,Xu, Jiaxi
, p. 6983 - 6990 (2006)
The stereochemistry is one of the critical issues in the Staudinger reaction. We have proposed the origin of the stereoselectivity recently. The effects of solvents, additives, and pathways of ketene generation on the stereoselectivity were investigated b
A telescopic one-pot synthesis of β-lactam rings using amines as a convenient source of imines
Rajam?ki, Suvi H. M.,De Luca, Lidia,Capitta, Francesca,Porcheddu, Andrea
, p. 38553 - 38557 (2016/06/01)
A facile synthetic approach to substituted β-lactams was designed, using secondary benzylic amines and acid chlorides as starting materials. The reactions proceeded smoothly and all the products were obtained in good yields.
Electrochemical generation and reactions of acyloxytriphenylphosphonium ions
Ohmori, Hidenobu,Maeda, Hatsuo,Kikuoka, Masayuki,Maki, Toshihide,Masui, Masaichiro
, p. 767 - 776 (2007/10/02)
Constant-current electrolysis, in an undivided cell, of Ph3P in the presence of a carboxylic acid in CH2Cl2 containing 2,6-lutidinium perchlorate as the supporting electrolyte was shown to generate the corresponding acyloxyphosphonium ion, Ph3P+-OCOR, which was converted in situ to esters, amides, and β-lactams under mild conditions.
