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Enantioselective Friedel-Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline-Cu(OTf)2.
Chem Commun (Camb). 2004 Feb 21CC

Abstract

The cheap and simple (i)Pr-bisoxazoline-Cu(OTf)(2) proves to be an efficient catalyst in the asymmetric Friedel-Crafts reaction of indole with arylidene malonates. In (i)BuOH, the S-enantiomer was obtained in up to 97% ee, while the opposite enantiomer was obtained in up to 78% ee in CH(2)Cl(2) or TTCE.

Authors+Show Affiliations

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, P. R. China.No affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

14765244

Citation

Zhou, Jian, and Yong Tang. "Enantioselective Friedel-Crafts Reaction of Indoles With Arylidene Malonates Catalyzed By IPr-bisoxazoline-Cu(OTf)2." Chemical Communications (Cambridge, England), 2004, pp. 432-3.
Zhou J, Tang Y. Enantioselective Friedel-Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline-Cu(OTf)2. Chem Commun (Camb). 2004.
Zhou, J., & Tang, Y. (2004). Enantioselective Friedel-Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline-Cu(OTf)2. Chemical Communications (Cambridge, England), (4), 432-3.
Zhou J, Tang Y. Enantioselective Friedel-Crafts Reaction of Indoles With Arylidene Malonates Catalyzed By IPr-bisoxazoline-Cu(OTf)2. Chem Commun (Camb). 2004 Feb 21;(4)432-3. PubMed PMID: 14765244.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Enantioselective Friedel-Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline-Cu(OTf)2. AU - Zhou,Jian, AU - Tang,Yong, Y1 - 2004/01/19/ PY - 2004/2/7/pubmed PY - 2004/2/7/medline PY - 2004/2/7/entrez SP - 432 EP - 3 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) IS - 4 N2 - The cheap and simple (i)Pr-bisoxazoline-Cu(OTf)(2) proves to be an efficient catalyst in the asymmetric Friedel-Crafts reaction of indole with arylidene malonates. In (i)BuOH, the S-enantiomer was obtained in up to 97% ee, while the opposite enantiomer was obtained in up to 78% ee in CH(2)Cl(2) or TTCE. SN - 1359-7345 UR - https://www.unboundmedicine.com/medline/citation/14765244/Enantioselective_Friedel_Crafts_reaction_of_indoles_with_arylidene_malonates_catalyzed_by_iPr_bisoxazoline_Cu_OTf_2_ DB - PRIME DP - Unbound Medicine ER -
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