Enantioselective N-heterocyclic carbene-catalyzed synthesis of indenopyrones-Reference-Cited by-同舟云学术

Enantioselective N-heterocyclic carbene-catalyzed synthesis of indenopyrones

Published:2015 Issue:24 Volume:13 Page:6694-6697
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Chen Kun-Quan¹²³⁴⁵,Zhang Han-Ming⁵⁶⁷⁸⁹,Wang Dong-Ling¹²³⁴⁵,Sun De-Qun¹²³⁴,Ye Song⁵⁶⁷⁸⁹

Affiliation:

1. Marine College

2. Shangdong University at Weihai

3. Weihai 264209

4. China

5. Beijing National Laboratory for Molecular Sciences

6. CAS Key Laboratory of Molecular Recognition and Function

7. Institute of Chemistry

8. Chinese Academy of Sciences

9. Beijing 100190

Abstract

Chiral disubstituted indenopyrones were synthesized in high yields with exclusive cis-selectivity and excellent enantioselectivity via N-heterocyclic carbene catalysis.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB00859J

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1. Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors

2. Design, Synthesis, and Structure−Activity Relationships of a Series of 3-[2-(1-Benzylpiperidin-4-yl)ethylamino]pyridazine Derivatives as Acetylcholinesterase Inhibitors

3. Correlations between Cytotoxicity and Topography of Some 2-Arylidenebenzocycloalkanones Determined by X-ray Crystallography

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5. Synthesis of Cytotoxic Indenoisoquinoline Topoisomerase I Poisons

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