Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Joseph E. Banning"'
Autor:
Edward F. C. Byrd, Jesse J. Sabatini, Joshua A. Orlicki, Lucille A. Wells, Joseph E Banning, Rosario C. Sausa, Eric C. Johnson, David E. Chavez
Publikováno v:
ChemPlusChem. 85:237-239
The synthesis and crystal structure of the heterocyclic explosive bis(nitroxymethylisoxazolyl) furoxan, C10 H6 N6 O10 , are described. In addition, we report its physical properties and theoretical performance. This material was found to exhibit stan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::973465f26fe7cdee928d6ff6b7f2b35d
https://doi.org/10.1002/cplu.201900710
https://doi.org/10.1002/cplu.201900710
Publikováno v:
Propellants, Explosives, Pyrotechnics. 39:670-676
A new method for the preparation of tetranitroglycoluril (TNGU, Sorguyl) is described, in which imidazo-[4,5-d]-imidazoles are nitrated with the elimination of N2O to generate TNGU. This method of TNGU synthesis results in material that is less sensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fcfa44f4b0179b53f312f24ea991957
https://doi.org/10.1002/prep.201400041
https://doi.org/10.1002/prep.201400041
Two ether-linked nitramines explosives have been synthesized. The reactivity of ether-linked nitramines has been probed and it was found that with heating, it is possible to perform a ring contraction to a methylene-linked nitramines that may be suit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95e3bcf23e5575bf0c3ab1d614e95e68
https://doi.org/10.21236/ad1012048
https://doi.org/10.21236/ad1012048
Publikováno v:
Organic Letters. 12:3968-3971
A chemo- and diastereoselective protocol for the formal nucleophilic substitution of 2-bromocyclopropylcarboxamides with secondary amides is described. This method allows for convergent and highly selective synthesis of trans-β-aminocyclopropane car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18af759c86afaa07d7c1b74d26294bb5
https://doi.org/10.1021/ol101228k
https://doi.org/10.1021/ol101228k
Publikováno v:
Organic Letters. 12:1488-1491
A new, general, and chemoselective protocol for the formal nucleophilic substitution of 2-bromocyclopropylcarboxamides is described. A wide range of alcohols and phenols can be employed as pronucleophiles in this transformation, providing expeditious
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e92d1060bc800106f1b98d9cba11615
https://doi.org/10.1021/ol100187c
https://doi.org/10.1021/ol100187c
Autor:
Joseph E. Banning, William M. Sherrill
A new, spherical morphology of tetranitroglycoluril (TNGU) has been prepared from the solvent, anti-solvent interaction of nitric acid and dichloromethane. This spherical morphology is significantly less sensitive to impact, friction, and static disc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30d741251d21aeab683b4a88a41591c9
https://doi.org/10.21236/ada602266
https://doi.org/10.21236/ada602266
Autor:
Joseph E. Banning, Marina Rubina, Michael Rubin, Andrew Rogers, Ivan A. Babkov, Andrew J. Edwards, Andrew Holtzen, Anthony R. Prosser, Pavel Ryabchuk, Jacob Gentillon
Publikováno v:
ChemInform. 44
The formation of cyclopropanes catalyzed by 18-crown-6 gives products with high diastereoselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ff9e7c54b60055a0d92c583337d9489
https://doi.org/10.1002/chin.201351055
https://doi.org/10.1002/chin.201351055
Autor:
Ivan A. Babkov, Jacob Gentillon, Marina Rubina, Anthony R. Prosser, Pavel Ryabchuk, Michael Rubin, Joseph E. Banning, Andrew J. Edwards, Andrew Holtzen, Andrew Rogers
Publikováno v:
The Journal of organic chemistry. 78(15)
A highly chemo- and diastereoselective protocol toward amino-substituted donor−acceptor cyclopropanes via the formal nucleophilic displacement in bromocyclopropanes is described. A wide range of N-nucleophiles, including carboxamides, sulfonamides,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cef141a6289209856e509fc6a1d6e5e3
https://pubmed.ncbi.nlm.nih.gov/23845068
https://pubmed.ncbi.nlm.nih.gov/23845068
Autor:
Jason Smarker, Michael Rubin, Joseph E. Banning, Marina Rubina, Anthony R. Prosser, Bassam K. Alnasleh
Publikováno v:
ChemInform. 42
The reaction of bromocyclopropanes with oxygen nucleophiles selectively provides trans- or cis-functionalized derivatives depending on the number and nature of cyclopropane substituents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6ac8993a2d390e29de607b88ec6916
https://doi.org/10.1002/chin.201133046
https://doi.org/10.1002/chin.201133046
Autor:
Michael Rubin, Marina Rubina, Bassam K. Alnasleh, Anthony R. Prosser, Jason Smarker, Joseph E. Banning
Publikováno v:
The Journal of organic chemistry. 76(10)
A diastereoconvergent formal nucleophilic substitution of bromocyclopropanes with oxygen- and sulfur-based nucleophiles is described. The reaction proceeds via in situ formation of a highly reactive cyclopropene intermediate and subsequent diastereos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c726c140cc76fd4638df1d3c9d351202
https://pubmed.ncbi.nlm.nih.gov/21462995
https://pubmed.ncbi.nlm.nih.gov/21462995