Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Richard G. Gillis"'
Publikováno v:
Organic Mass Spectrometry. 26:247-249
Under electron impact, the molecular ions of quinoline N-oxide, carbostyril and 8-hydroxyquinoline lose carbon monoxide giving a fragment ion C8H7N (m/z 117), which was shown by collision-activated dissociation in each case to have the structure of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17722f34f52a0d71823b669dc136e969
https://doi.org/10.1002/oms.1210260412
https://doi.org/10.1002/oms.1210260412
Autor:
Richard G. Gillis
Publikováno v:
Organic Mass Spectrometry. 21:415-418
Under positive ion chemical ionization conditions with ammonla at relatively low pressure, aromatic nitro compounds do not form [M + H]+ ions but often form ionic clusters [M + NH4]+ and [M + N2H7]+. Nitrobenzene forms a cluster [2M + NH4]+ and anili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::217db37d79443db32f561de1aa15ce7e
https://doi.org/10.1002/oms.1210210707
https://doi.org/10.1002/oms.1210210707
Autor:
Richard G. Gillis, Charles C. Price
Publikováno v:
Journal of the American Chemical Society. 75:4750-4753
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::260b23aba6a9370dab681949401ef0ed
https://doi.org/10.1021/ja01115a040
https://doi.org/10.1021/ja01115a040
Autor:
Richard G. Gillis
Publikováno v:
The Journal of Organic Chemistry. 21:805-808
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7db1a1324ec5b12a17bd4e33d15ba69a
https://doi.org/10.1021/jo01113a609
https://doi.org/10.1021/jo01113a609
Autor:
Quentin N. Porter, Richard G. Gillis
Publikováno v:
Organic Mass Spectrometry. 20:82-84
The molecular ion of o-methoxy-d3-benzoic acid can undergo three different rearrangements and hydrogen/deuterium exchange between the functional groups. This can result in 14 isomers of the molecular ion before it decomposes giving fragments at m/z 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e470477c7e3a8fd7eac367b7f44c33b
https://doi.org/10.1002/oms.1210200203
https://doi.org/10.1002/oms.1210200203
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b8158770504398fdea9f3d4a77b276a
https://doi.org/10.1002/chin.197530119
https://doi.org/10.1002/chin.197530119
Publikováno v:
Organic Mass Spectrometry. 19:199-199
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ca6c0fc5817ae978848bc792bacda8c
https://doi.org/10.1002/oms.1210190413
https://doi.org/10.1002/oms.1210190413
Autor:
Richard G. Gillis
Publikováno v:
Journal of Chemical Education. 31:344
Recent investigation has shown conclusively that the diazotization reaction is between free base and a number of Lewis acids, of which one or more be effective at any one time.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4914fd02cb8c17f7a7423a955101624f
https://doi.org/10.1021/ed031p344
https://doi.org/10.1021/ed031p344
Autor:
Richard G. Gillis, Peter F. Nelson
Publikováno v:
Journal of Chemical Education. 31:546
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b83eb00931907b1a97dc216c27dc96a4
https://doi.org/10.1021/ed031p546
https://doi.org/10.1021/ed031p546