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Enantioselective synthesis of cyclopropylcarboxamides using s-BuLi-sparteine-mediated metallation.
Chem Commun (Camb). 2008 Nov 14CC

Abstract

Enantioselective synthesis of cyclopropylcarboxamides is possible by asymmetric metallation of prochiral starting cyclopropanes using s-BuLi-sparteine.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Lauru S
School of Chemistry, The University of Nottingham, University Park, Nottingham, UK.
Simpkins NS
No affiliation info available
Gethin D
No affiliation info available
Wilson C
No affiliation info available

MeSH

AmidesCatalysisCrystallography, X-RayCyclopropanesLithiumModels, MolecularMolecular StructureSparteineStereoisomerism

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

18985220

Citation

Lauru, Stephanie, et al. "Enantioselective Synthesis of Cyclopropylcarboxamides Using s-BuLi-sparteine-mediated Metallation." Chemical Communications (Cambridge, England), 2008, pp. 5390-2.
Lauru S, Simpkins NS, Gethin D, et al. Enantioselective synthesis of cyclopropylcarboxamides using s-BuLi-sparteine-mediated metallation. Chem Commun (Camb). 2008.
Lauru, S., Simpkins, N. S., Gethin, D., & Wilson, C. (2008). Enantioselective synthesis of cyclopropylcarboxamides using s-BuLi-sparteine-mediated metallation. Chemical Communications (Cambridge, England), (42), 5390-2. https://doi.org/10.1039/b810441g
Lauru S, et al. Enantioselective Synthesis of Cyclopropylcarboxamides Using s-BuLi-sparteine-mediated Metallation. Chem Commun (Camb). 2008 Nov 14;(42)5390-2. PubMed PMID: 18985220.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Enantioselective synthesis of cyclopropylcarboxamides using s-BuLi-sparteine-mediated metallation. AU - Lauru,Stephanie, AU - Simpkins,Nigel S, AU - Gethin,David, AU - Wilson,Claire, Y1 - 2008/09/16/ PY - 2008/11/6/pubmed PY - 2009/1/24/medline PY - 2008/11/6/entrez SP - 5390 EP - 2 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) IS - 42 N2 - Enantioselective synthesis of cyclopropylcarboxamides is possible by asymmetric metallation of prochiral starting cyclopropanes using s-BuLi-sparteine. SN - 1359-7345 UR - https://www.unboundmedicine.com/medline/citation/18985220/Enantioselective_synthesis_of_cyclopropylcarboxamides_using_s_BuLi_sparteine_mediated_metallation_ L2 - https://doi.org/10.1039/b810441g DB - PRIME DP - Unbound Medicine ER -