reference/28906520

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/28906520

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endingPage	2813
issn	0022-3263 1520-6904
issueIdentifier	8
pageRange	2807-2813
publicationName	The Journal of Organic Chemistry
startingPage	2807
bibliographicCitation	Yao Y, Fan W, Li W, Ma X, Zhu L, Xie X, Zhang Z. Synthesis of (S)-7-amino-5-azaspiro[2.4]heptane via highly enantioselective hydrogenation of protected ethyl 1-(2-aminoaceto)cyclopropanecarboxylates. J Org Chem. 2011 Apr 15;76(8):2807–13. doi: 10.1021/jo2002165. PMID: 21413753.
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date	2011-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/21413753 https://doi.org/10.1021/jo2002165
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Synthesis of (S)-7-Amino-5-azaspiro[2.4]heptane via Highly Enantioselective Hydrogenation of Protected Ethyl 1-(2-Aminoaceto)cyclopropanecarboxylates
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Total number of triples: 54.