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Asymmetric dearomatization of β-naphthols through an amination reaction catalyzed by a chiral phosphoric acid.
Angew Chem Int Ed Engl. 2015 Jan 07; 54(2):647-50.AC

Abstract

A highly efficient catalytic asymmetric dearomatization of naphthols by means of an electrophilic amination reaction catalyzed by chiral phosphoric acid is presented. This protocol provides a facile access to functionalized β-naphthalenone compounds with a chiral quaternary carbon center in excellent yields and enantioselectivity (up to 99% yield, up to 96% ee).

Authors+Show Affiliations

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032 (China) http://shuliyou.sioc.ac.cn/No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

25414091

Citation

Wang, Shou-Guo, et al. "Asymmetric Dearomatization of Β-naphthols Through an Amination Reaction Catalyzed By a Chiral Phosphoric Acid." Angewandte Chemie (International Ed. in English), vol. 54, no. 2, 2015, pp. 647-50.
Wang SG, Yin Q, Zhuo CX, et al. Asymmetric dearomatization of β-naphthols through an amination reaction catalyzed by a chiral phosphoric acid. Angew Chem Int Ed Engl. 2015;54(2):647-50.
Wang, S. G., Yin, Q., Zhuo, C. X., & You, S. L. (2015). Asymmetric dearomatization of β-naphthols through an amination reaction catalyzed by a chiral phosphoric acid. Angewandte Chemie (International Ed. in English), 54(2), 647-50. https://doi.org/10.1002/anie.201409756
Wang SG, et al. Asymmetric Dearomatization of Β-naphthols Through an Amination Reaction Catalyzed By a Chiral Phosphoric Acid. Angew Chem Int Ed Engl. 2015 Jan 7;54(2):647-50. PubMed PMID: 25414091.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Asymmetric dearomatization of β-naphthols through an amination reaction catalyzed by a chiral phosphoric acid. AU - Wang,Shou-Guo, AU - Yin,Qin, AU - Zhuo,Chun-Xiang, AU - You,Shu-Li, Y1 - 2014/11/20/ PY - 2014/10/04/received PY - 2014/11/22/entrez PY - 2014/11/22/pubmed PY - 2014/11/22/medline KW - amination reaction KW - asymmetric catalysis KW - dearomatization KW - naphthol KW - organocatalysis SP - 647 EP - 50 JF - Angewandte Chemie (International ed. in English) JO - Angew Chem Int Ed Engl VL - 54 IS - 2 N2 - A highly efficient catalytic asymmetric dearomatization of naphthols by means of an electrophilic amination reaction catalyzed by chiral phosphoric acid is presented. This protocol provides a facile access to functionalized β-naphthalenone compounds with a chiral quaternary carbon center in excellent yields and enantioselectivity (up to 99% yield, up to 96% ee). SN - 1521-3773 UR - https://www.unboundmedicine.com/medline/citation/25414091/Asymmetric_dearomatization_of_��_naphthols_through_an_amination_reaction_catalyzed_by_a_chiral_phosphoric_acid_ DB - PRIME DP - Unbound Medicine ER -
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