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Asymmetric organocatalytic Michael addition of anthrone to enone.
Org Biomol Chem. 2010 Jul 21; 8(14):3244-50.OB

Abstract

Catalyzed by the bifunctional tertiary amino-thiourea organocatalyst derived from epicinchona alkaloid, the asymmetric Michael addition of anthrone to enone was achieved in high yield with excellent enantioselectivity.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Wu C
Engineering Research Centre of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Li W
No affiliation info available
Yang J
No affiliation info available
Liang X
No affiliation info available
Ye J
No affiliation info available

MeSH

AnthracenesCatalysisCinchona AlkaloidsCross-Linking ReagentsKetonesStereoisomerismThiourea

Pub Type(s)

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

Language

eng

PubMed ID

20495718

Citation

Wu, Chunlin, et al. "Asymmetric Organocatalytic Michael Addition of Anthrone to Enone." Organic & Biomolecular Chemistry, vol. 8, no. 14, 2010, pp. 3244-50.
Wu C, Li W, Yang J, et al. Asymmetric organocatalytic Michael addition of anthrone to enone. Org Biomol Chem. 2010;8(14):3244-50.
Wu, C., Li, W., Yang, J., Liang, X., & Ye, J. (2010). Asymmetric organocatalytic Michael addition of anthrone to enone. Organic & Biomolecular Chemistry, 8(14), 3244-50. https://doi.org/10.1039/b927421a
Wu C, et al. Asymmetric Organocatalytic Michael Addition of Anthrone to Enone. Org Biomol Chem. 2010 Jul 21;8(14):3244-50. PubMed PMID: 20495718.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Asymmetric organocatalytic Michael addition of anthrone to enone. AU - Wu,Chunlin, AU - Li,Wenjun, AU - Yang,Juanjuan, AU - Liang,Xinmiao, AU - Ye,Jinxing, Y1 - 2010/05/21/ PY - 2010/5/25/entrez PY - 2010/5/25/pubmed PY - 2010/10/12/medline SP - 3244 EP - 50 JF - Organic & biomolecular chemistry JO - Org Biomol Chem VL - 8 IS - 14 N2 - Catalyzed by the bifunctional tertiary amino-thiourea organocatalyst derived from epicinchona alkaloid, the asymmetric Michael addition of anthrone to enone was achieved in high yield with excellent enantioselectivity. SN - 1477-0539 UR - https://www.unboundmedicine.com/medline/citation/20495718/Asymmetric_organocatalytic_Michael_addition_of_anthrone_to_enone_ L2 - https://doi.org/10.1039/b927421a DB - PRIME DP - Unbound Medicine ER -