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l‑Proline as a Valuable Scaffold for the Synthesis of Novel..:
Israel Bonilla-Landa (10036566)
;
Ulises Cuapio-Muñoz (10036569)
;
Axel Luna-Hernández (10036572)
...
https://figshare.com/articles/journal_contribution/l_Proline_as_a_Valuable_Scaffold_for_the_Synthesis_of_Novel_Enantiopure_Neonicotinoids_Analogs/13645842. , 1753
Link:
https://doi.org/10.1021/acs.jafc.0c05997.s001
RT Journal T1
l‑Proline as a Valuable Scaffold for the Synthesis of Novel Enantiopure Neonicotinoids Analogs
UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_13645842&Exemplar=1&LAN=DE A1 Israel Bonilla-Landa (10036566) A1 Ulises Cuapio-Muñoz (10036569) A1 Axel Luna-Hernández (10036572) A1 Alfonso Reyes-Luna (10036575) A1 Alfredo Rodríguez-Hernández (10036578) A1 Arturo Ibarra-Juarez (10036581) A1 Gabriel Suarez-Mendez (10036584) A1 Felipe Barrera-Méndez (10036587) A1 Nadia Caram-Salas (1963165) A1 J. Francisco Enríquez-Medrano (10036590) A1 Ramón E. Díaz de León (10036593) A1 José Luis Olivares-Romero (10036596) YR 1753 K1 Biochemistry K1 Neuroscience K1 Pharmacology K1 Infectious Diseases K1 Biological Sciences not elsewhere classified K1 Chemical Sciences not elsewhere classified K1 Information Systems not elsewhere classified K1 compound 9 K1 insecticide K1 Novel Enantiopure Neonicotinoids An K1 l-proline K1 dinotefuran K1 neonicotinoid JF https://figshare.com/articles/journal_contribution/l_Proline_as_a_Valuable_Scaffold_for_the_Synthesis_of_Novel_Enantiopure_Neonicotinoids_Analogs/13645842 LK http://dx.doi.org/https://doi.org/10.1021/acs.jafc.0c05997.s001 DO https://doi.org/10.1021/acs.jafc.0c05997.s001 SF ELIB - SuUB Bremen
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