Propynal Equivalents and Diazopropyne: Synthesis of All Mono??13C Isotopomers
RA Seburg, JA Hodges, RJ McMahon
Index: Seburg, Randal A.; Hodges, Jonathan A.; McMahon, Robert J. Helvetica Chimica Acta, 2009 , vol. 92, # 8 p. 1626 - 1643
Full Text: HTML
Citation Number: 3
Abstract
Abstract Mechanistic and spectroscopic investigations of reactive C 3 H 2 hydrocarbons necessitated the preparation of diazopropyne isotopomers bearing mono-13 C substitution at each of the three unique positions. The diazo compounds and their tosylhydrazone precursors were prepared from the mono-13 C isotopomers of propynal (in the form of either the aldehyde or the diethyl acetal). The introduction of 13 C-labeling at either alkyne ...
Related Articles:
[Stambouli, A.; Chastrette, F.; Amouroux, R.; Chastrette, M.; Mattioda, G.; Blanc, A. Tetrahedron Letters, 1986 , vol. 27, # 35 p. 4149 - 4152]
[Stambouli, A.; Chastrette, F.; Amouroux, R.; Chastrette, M.; Mattioda, G.; Blanc, A. Tetrahedron Letters, 1986 , vol. 27, # 35 p. 4149 - 4152]