The asymmetric Cu(ii)–indolinylmethanol complex catalyzed Diels–Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters: an efficient route to functionalized tetrahydrocarbazoles-Reference-Cited by-同舟云学术

The asymmetric Cu(ii)–indolinylmethanol complex catalyzed Diels–Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters: an efficient route to functionalized tetrahydrocarbazoles

Published:2014 Issue:24 Volume:12 Page:4172-4176
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Ouyang Banlai¹²³⁴,Yu Tingting¹²³⁴,Luo Renshi¹²³⁴,Lu Gui¹²³⁴⁵

Affiliation:

1. Institute of Medicinal Chemistry

2. School of Pharmaceutical Sciences

3. Sun Yat-sen University

4. Guangzhou 510006, P. R. China

5. Institute of Human Virology

Abstract

An efficient asymmetric Diels–Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters for the synthesis of functionalized tetrahydrocarbazoles.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB00196F

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3. Vinca Alkaloids. X1. The Structure of Vindoline

4. Asymmetric Total Synthesis of Vindoline

5. Catalytic Asymmetric Michael Reaction of β-Keto Esters: Effects of the Linker Heteroatom in Linked-BINOL

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