III.1 Some Reactions of Bis-(trifluoromethyl)-amine, (CF3)2NH2 ... Yu , Whiting N. Shepard , James A. Magnuson , Richard A. Porter , and Jean'ne M. Sh...
Fluorocarbon Nitrogen Compounds. III.1 Some Reactions of Bis-(trifluoromethyl)-amine, (CF3)2NH2. John A. Young ... Click to increase image size Free first page. View: PDF | PDF w/ Links ... Hg[P(CF3)2]2. Joseph Grobe , Reinhard Demuth. Angewandte Che
Fluorocarbon Nitrogen Compounds. III.1 Some Reactions ...https://pubs.acs.org/doi/pdfplus/10.1021/ja01547a030by JA Young - â1958 - âCited by 55 - âRelated articles.ilthough hydrocarbon alkyls of nitrogen form only one series of compounds, the a
O F CHEMICAL ENGINEERING, UNIVERSITY OF FLORIDA] ... which (CHs)zNCOCl gives the best yield. ... fragmentation, the best yield of ti e perfluoro car-.
1 hour since most of the carbinol was recovered unchanged. ... minutes at room temperature was raised to boiling over 1 minute .... A perfluoroamino acid, ( CFa)2NCFzCOOH, has been synthesized by the ..... Fraction 6, b.p. 22 to 26", mol. wt.
WILLIAM S. DURRELL,~ JOHN A. YOUNG, AXD RICHARD D. DRESDNER. Departments of Chemistry and Chemical Engineering, Il'nizlersit y of Florida, ...
John A. Young and Robert L. Dressler. Chemical Division, Denver Research Institute, University of Denver, Denver, Colorado. Received October 19, 1966.
Fluorocarbon nitrogen compounds. XI. Functionally active perfluoroalkyl-substituted s-triazines. John Adams Young, and Robert L. Dressler. J. Org. Chem.
123. Preparation and reactions of bis(aminoboryl) oxides. M. Komorowska, K. Niedenzu, and W. Weber. Inorg. Chem. , 1990, 29 (2), pp 289â294. DOI: 10.1021/ ...
Jan 1, 1990 - 123. Preparation and reactions of bis(aminoboryl) oxides. M. Komorowska, K. ... and Application to Concise Synthesis of Defucogilvocarcin M.
Selective cyclisation of 2, 3, 4, 5-tetra-O-acetyl-galactaric acid bis-[Alkylthio(thiocarbonyl)]hydrazide to Saccharide 1, 3, 4-Oxadiazole, Thiadiazole, and ...
.ilthough hydrocarbon alkyls of nitrogen form ably above room temperature in order to drive off only one series of compounds, the amines (RNHr, the amine completely. I