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Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt.
Org Biomol Chem. 2010 Jun 28; 8(13):3031-6.OB

Abstract

Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by asymmetric catalysis with L-phenylalanine lithium salt, giving gamma-nitroaldehydes in good yields with high enantioselectivity.

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Publisher Full Text (DOI)

Authors+Show Affiliations

Yoshida M
Division of Chemical Process Engineering, Graduate School of Engineering, Hokkaido University, 8, Kita 13-jo Nishi, Kita-ku, 060-8628, Sapporo, Japan. myoshida@eng.hokudai.ac.jp
Sato A
No affiliation info available
Hara S
No affiliation info available

MeSH

AldehydesAlkenesAmino AcidsCatalysisLithiumSalts

Pub Type(s)

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

Language

eng

PubMed ID

20461274

Citation

Yoshida, Masanori, et al. "Asymmetric Michael Addition of Aldehydes to Nitroalkenes Using a Primary Amino Acid Lithium Salt." Organic & Biomolecular Chemistry, vol. 8, no. 13, 2010, pp. 3031-6.
Yoshida M, Sato A, Hara S. Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt. Org Biomol Chem. 2010;8(13):3031-6.
Yoshida, M., Sato, A., & Hara, S. (2010). Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt. Organic & Biomolecular Chemistry, 8(13), 3031-6. https://doi.org/10.1039/c003940c
Yoshida M, Sato A, Hara S. Asymmetric Michael Addition of Aldehydes to Nitroalkenes Using a Primary Amino Acid Lithium Salt. Org Biomol Chem. 2010 Jun 28;8(13):3031-6. PubMed PMID: 20461274.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt. AU - Yoshida,Masanori, AU - Sato,Atsushi, AU - Hara,Shoji, Y1 - 2010/05/12/ PY - 2010/5/13/entrez PY - 2010/5/13/pubmed PY - 2010/9/18/medline SP - 3031 EP - 6 JF - Organic & biomolecular chemistry JO - Org Biomol Chem VL - 8 IS - 13 N2 - Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by asymmetric catalysis with L-phenylalanine lithium salt, giving gamma-nitroaldehydes in good yields with high enantioselectivity. SN - 1477-0539 UR - https://www.unboundmedicine.com/medline/citation/20461274/Asymmetric_Michael_addition_of_aldehydes_to_nitroalkenes_using_a_primary_amino_acid_lithium_salt_ L2 - https://doi.org/10.1039/c003940c DB - PRIME DP - Unbound Medicine ER -