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dc.contributor.author | DE LA CRUZ CORDERO, RICARDO ABRAHAM | |
dc.contributor.author | LABASTIDA GALVAN, VICTORIA | |
dc.contributor.author | FERNANDEZ ZERTUCHE, MARIO | |
dc.contributor.author | ORDOÑEZ PALACIOS, JOSE MARIO | |
dc.creator | DE LA CRUZ CORDERO, RICARDO ABRAHAM; 121952 | |
dc.creator | LABASTIDA GALVAN, VICTORIA; 509032 | |
dc.creator | FERNANDEZ ZERTUCHE, MARIO; 15480 | |
dc.creator | ORDOÑEZ PALACIOS, JOSE MARIO; 16485 | |
dc.date.accessioned | 2016-03-16T17:17:29Z | |
dc.date.available | 2016-03-16T17:17:29Z | |
dc.date.issued | 2005 | |
dc.identifier | http://www.redalyc.org/articulo.oa?id=47549404 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11799/39328 | |
dc.description | Reduction of (3S)-N,N-dibenzylamino-2-ketophosphonates 9a-d derived from L-amino acids was carried out with catecholborane at -20 oC to afford the (3S)-N,N-dibenzylamino-(2R)-hydroxy-phosphonates syn-10a-d, whereas the reduction of (3S)-N-benzylamino-2- ketophosphonates 13a-d with Zn(BH4)2 at -78 oC yield (3S)-N-benzylamino-( 2S)-hydroxyphosphonates anti-14a-d. The reduction in both cases was in good chemical yields and with high diastereoselectivity. The hydrolysis and hydrogenolysis of 10a-d and 14a-d afford the (3S)-amino-(2R)-hydroxyphosphonic acids 6 and (3S)-amino-(2S)- hydroxyphosphonic acids 7, respectively, which are analogues of phosphostatine. | |
dc.format | application/pdf | |
dc.language.iso | eng | es |
dc.publisher | Sociedad Química de México | |
dc.relation | http://www.redalyc.org/revista.oa?id=475 | |
dc.rights | openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0 | |
dc.source | Journal of the Mexican Chemical Society (México) Num.4 Vol.49 | |
dc.subject | Química | es |
dc.subject | Phosphostatine | es |
dc.subject | aminophosphonic acids | es |
dc.subject | β-ketophosphonates, | es |
dc.subject | diastereoselective reduction | es |
dc.subject.classification | BIOLOGÍA Y QUÍMICA | |
dc.title | Preparation of Phosphostatine Analogues From L-amino acids | es |
dc.type | Artículo | es |
dc.provenance | Científica | es |
dc.road | Dorada | es |
dc.ambito | Internacional | es |
dc.audience | students | es |
dc.audience | researchers | es |
dc.type.conacyt | article | |
dc.identificator | 2 |
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