Synthesis of Highly Enantiomerically Enriched N-Boc-a-amino Ketones from Pseudoephedrine N-Boc-a-amino Acid Amides

dc.contributor.author	Myers, Andrew
dc.contributor.author	Yoon, Taeyoung
dc.date.accessioned	2009-06-26T17:07:09Z
dc.date.issued	1995
dc.identifier.citation	Myers, Andrew G. and Taeyoung Yoon. 1995. Synthesis of highly enantiomerically enriched N-Boc-a-amino ketones from pseudoephedrine N-Boc-a-amino acid amides. Tetrahedron Letters 36(52): 9429-9432.	en
dc.identifier.issn	0040-4039	en
dc.identifier.uri	http://nrs.harvard.edu/urn-3:HUL.InstRepos:3122541
dc.description.abstract	N-Boc-alpha-amino ketones are synthesized efficiently and in high enantiomeric excess by the addition of organolithium and Grignard reagents to pseudoephedrine amides of N-Boc-alpha-amino acids, themselves available by the alkylation of pseudoephedrine glycinamide followed by N-protection.	en
dc.description.sponsorship	Chemistry and Chemical Biology	en
dc.language.iso	en_US	en
dc.publisher	Elsevier	en
dc.relation.isversionof	http://dx.doi.org/10.1016/0040-4039(95)02053-5	en
dc.relation.hasversion	http://www.chem.harvard.edu/groups/myers/pdf_publications/tetlet_1995_36_9429.pdf	en
dash.license	META_ONLY
dc.title	Synthesis of Highly Enantiomerically Enriched N-Boc-a-amino Ketones from Pseudoephedrine N-Boc-a-amino Acid Amides	en
dc.type	Journal Article
dc.description.version	Version of Record
dc.relation.journal	Tetrahedron Letters	en
dash.depositing.author	Myers, Andrew
dash.embargo.until	10000-01-01
dc.identifier.doi	10.1016/0040-4039(95)02053-5	*
dash.contributor.affiliated	Myers, Andrew