Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Domitila Aparicio"'
Publikováno v:
ARKIVOC, Vol 2005, Iss 9, Pp 405-414 (2005)
Externí odkaz:
https://doaj.org/article/8e75588a0836448c92ec33f1162c6298
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 153-161 (2005)
Externí odkaz:
https://doaj.org/article/c8bcb789c7684cca9ecde67d9b3ce034
Autor:
Pedro Romón, Juan Carlos Iturrondobeitia, Arturo Goldarazena, Francisco Palacios, Thierry Hance, Domitila Aparicio
Publikováno v:
Journal of Insect Science, Vol. 15, no.5, p. 1–6 (2017)
Journal of Insect Science
Journal of Insect Science
Concentrations of four monoterpenes were determined in needles of Pinus radiata (D.Don) (Pinales: Pinaceae) trees that were attacked or nonattacked by Tomicus piniperda (L.) (Coleoptera: Scolytinae). Compounds were identified and quantified by gas ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2773e2c3386f3bc937ca1ad7345fcd30
https://hdl.handle.net/2078.1/227782
https://hdl.handle.net/2078.1/227782
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 186:735-741
An efficient method for the synthesis of phosphorated 1,2-oxazabuta-1,3-dienes derived from phosphine oxides and phosphonates has been developed by means of base-mediated dehydrohalogenation of readily available α-halooximes. New functionalized α-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99e17de11dd3f1230bfe95672d37e83e
https://doi.org/10.1080/10426507.2010.522632
https://doi.org/10.1080/10426507.2010.522632
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 186:638-643
The synthesis of α-iminophosphonates derived from ketones has been achieved by aza-Wittig reaction of P-trimethylphosphazenes with acylphosphonates. These unstable compounds can be used for the synthesis of chiral α-aminophosphonate derivatives thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14b4b2ac1e4d8d864973ec4b2b84ea2e
https://doi.org/10.1080/10426507.2010.521211
https://doi.org/10.1080/10426507.2010.521211
Publikováno v:
The Journal of Organic Chemistry. 74:452-455
Aza-Michael reaction of ammonia, aliphatic, aromatic and optically active amines to an α,β-unsaturated imine derived from α-aminophosphonate affords α-dehydroaminophosphonates with a γ-stereogenic center bearing an amino group. Resulting γ-amin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::697bf0bf1024a8b2a6119abb74ee7350
https://doi.org/10.1021/jo8022022
https://doi.org/10.1021/jo8022022
Autor:
Paolino Filippone, Fabio Mantellini, Francisco Palacios, Roberto Ignacio, Simona Nicolini, Jesús M. de los Santos, Domitila Aparicio, Samuele Lillini, Orazio A. Attanasi
Publikováno v:
Tetrahedron. 64:9264-9274
The synthesis of substituted 2,3-dihydro-1,4-thiazines, fused cycloalkyl-1,4-thiazines, 1,4-benzothiazines and fused cycloalkyl-1,4-benzothiazines by 1,4-addition of 1,2-aminothiols to 1,2-diaza-1,3-dienes bearing carboxylate, carboxamide, or phospho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ad08bef4511406ea4efa9bffd3ab986
https://doi.org/10.1016/j.tet.2008.07.030
https://doi.org/10.1016/j.tet.2008.07.030
Publikováno v:
Tetrahedron Letters. 48:6747-6750
α,β-Unsaturated sulfinylimines derived from α-amino acids undergo aza-Diels–Alder reaction with electron rich dienophiles such as enolethers and enamines. Subsequent elimination of sulfinyl and amine or alkoxy moiety on the resulting cycloadduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43b669c949ad35ebb57fd577c3521ef6
https://doi.org/10.1016/j.tetlet.2007.07.101
https://doi.org/10.1016/j.tetlet.2007.07.101
Publikováno v:
The Journal of Organic Chemistry. 72:2682-2685
An efficient synthesis of α,β-unsaturated imines derived from α-aminophosphonates is achieved through aza-Wittig reaction of P-trimethyl phosphazenes with β,γ-unsaturated α-ketophosphonates. Selective 1,2-reduction of such 1-azadienes affords
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b8f230b55a1aedbcf18af38c1b2eb71
https://doi.org/10.1021/jo062609+
https://doi.org/10.1021/jo062609+
Publikováno v:
European Journal of Organic Chemistry. 2006:2843-2850
A very simple and efficient synthesis of 3-amino-1,5-dihydro-2H-pyrrol-2-ones is reported. These cyclic dehydro-amino acid derivatives with a stereogenic center at the 5-position were obtained by the addition of two equivalents of amine to β,γ-unsa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f40dc7cdb2824687f8ed6317aec758f6
https://doi.org/10.1002/ejoc.200600092
https://doi.org/10.1002/ejoc.200600092