Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Thomas G. Archibald"'
Publikováno v:
Implementation Science, Vol 15, Iss 1, Pp 1-20 (2020)
Abstract Background There is a need to unpack the empirical, practical, and personal challenges within participatory approaches advocated to optimize implementation. The unpredictable, chaotic nature of participatory approaches complicates applicatio
Externí odkaz:
https://doaj.org/article/18e6c0d517564c6bb01521ea8ca20d1c
Autor:
Simon G. Bott, William E. Stevens, Robert L. McKenney, Alan P. Marchand, Thomas G. Floyd, Thomas G. Archibald, G. V. M. Sharma
Publikováno v:
Journal of Energetic Materials. 16:1-22
The synthesis of TNDAZ in four steps by starting with N-t-butyl-3-hydroxymethyl-3-nitroazetidine is described. The structures of TNDAZ and of a precursor, N-t-butyl-3-nitro-3-(N'-t-butyl-3′-nitroazetidin-3′-yl) azetidine, have been established un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe9a6f6c90ddbf21d4f58a6dc0c66e70
https://doi.org/10.1080/07370659808216090
https://doi.org/10.1080/07370659808216090
Publikováno v:
Waste Management. 17:143-146
The original synthesis of TNAZ (1,3,3-trinitroazetidine) was developed by T. G. Archibald in 1983 and was scaled up to produce several hundred kg of TNAZ for evaluation by the DoD. Although the synthesis method utilizes inexpensive starting materials
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d94a9267a8a740346e8c985f3aa8053e
https://doi.org/10.1016/s0956-053x(97)10013-7
https://doi.org/10.1016/s0956-053x(97)10013-7
Autor:
Thomas G. Archibald, Clifford George, D. Tzeng, Richard Gilardi, Kurt Baum, Judith L. Flippen-Anderson
Publikováno v:
ChemInform. 22
1,2-Difluorodinitroethylene was synthesized by flash vacuum pyrolysis of 1,2-difluorotetranitroethane. X-ray crystallography showed that one of the two nitro groups is out of the plane of the rest of molecule and that the C-C double-bond distance in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4b93689d3f6879836140662d769e45c
https://doi.org/10.1002/chin.199131113
https://doi.org/10.1002/chin.199131113
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d44162d2e26e5359bfed5c1e57a0022c
https://doi.org/10.1002/chin.199436134
https://doi.org/10.1002/chin.199436134
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de39441a6614d1b90da18f850b72b78f
https://doi.org/10.1002/chin.199511128
https://doi.org/10.1002/chin.199511128
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84f4636859f70514a246518fa22bf6a9
https://doi.org/10.1002/chin.199550082
https://doi.org/10.1002/chin.199550082
Autor:
Nguyen Nghi Van, Richard Gilardi, Judith L. Flippen-Anderson, Clifford George, Thomas G. Archibald, Kurt Baum, Sean S. Bigelow
Publikováno v:
The Journal of Organic Chemistry. 57:235-241
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::add70dfb39b642cf9982021665ef1fdb
https://doi.org/10.1021/jo00027a042
https://doi.org/10.1021/jo00027a042
Autor:
Thomas G. Archibald, Kurt Baum
Publikováno v:
The Journal of Organic Chemistry. 55:3562-3565
This report describes a facile synthesis of isopropyl 2,2-difluorovinyl ketone and isopropyl 3,3-difluoroacrylate and some unusual addition reactions of these olefins with nitronate anions and β-nitro al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4cd58c656c54934183d46b5526c7f95
https://doi.org/10.1021/jo00298a034
https://doi.org/10.1021/jo00298a034
Publikováno v:
The Journal of Organic Chemistry. 55:2920-2924
1,3,3-Trinitroazetidine (1) was synthesized via a Mannich condensation and its structure elucidated by X-ray crystallography
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82b5f6739e2783691172049fb99c2bd3
https://doi.org/10.1021/jo00296a066
https://doi.org/10.1021/jo00296a066