Reaction of Terminal Alkynes with Hydrazines To Give Nitriles

José Luis Mata-Mata , J. Alfredo Gutiérrez , M. Angeles Paz-Sandoval , Amira R. Madrigal , Antonio Martínez-Richa. Journal of Polymer Science Part A: Polymer ...

Pavel Kočovský, Victoria Dunn, Adolf Gogoll, and Vratislav Langer. The Journal of Organic ... Ei-ichi Negishi, Denis Y. Kondakov, and David E. Van Horn.

Addition of dialkyl disulfides to terminal alkynes is catalyzed by a rhodium−phosphine complex and trifluoromethanesulfonic acid giving (Z)-bis(alkylthio)olefins ...

[email protected]. Received January 6, 2001. ABSTRACT. Addition of dialkyl disulfides to terminal alkynes is catalyzed by a rhodium−phosphine ...

For examples of bisphosphonate prodrugs, see: (a) Ezra, A.; Hoffman, A.; Breuer, E.; Alferiev, I. S.; Mönkkönen, J.; Hanany-Rozen, N. E.; Weiss, G.; Stepensky, D.

tion of terminal alkynes with organic halides in the presence of a catalytic ... the desired coupling reaction to proceed, but the product yield was decreased ...

Terminal alkynes react with allylamine in the presence of a RhCl(PPh3)3 catalyst to give (E)-3-alkylidene-3,4-dihydro-2H-pyrroles. The products consist of two ...

A Quantum Chemical Study of the Monomers: Ag2X, AgX, AgX2, and AgX3 (X = F, ... Chemistry - A European Journal 2016 22 (10), 3485-3490 .... Ligand-free copper(Ι)-catalyzed Sonogashira-type coupling of arylboronic acids ... of aryl iodides with termi

Dec 2, 2005 - Hypophosphorous Acid and Its Salts as Reagents in Organophosphorus Chemistry. Aurelia Visa , Bianca Maranescu , Gheorghe Ilia. 2016 ...

Sep 2, 2006 - Terminal alkynes react with allylamine in the presence of a RhCl(PPh3)3 catalyst to give (E)-3-alkylidene-3,4-dihydro-2H-pyrroles.