Preparation of 3,4,5-Trisubstituted Oxazolones by Pd-Catalyzed Coupling of N-Alkynyl tert-Butyloxycarbamates with Aryl Halides and Related Electrophiles-Reference-Cited by-同舟云学术

Preparation of 3,4,5-Trisubstituted Oxazolones by Pd-Catalyzed Coupling of N-Alkynyl tert-Butyloxycarbamates with Aryl Halides and Related Electrophiles

Published:2012-10-15 Issue:21 Volume:77 Page:9871-9877
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lu Zenghui¹,Cui Weijian¹,Xia Siyuan¹,Bai Yihui¹,Luo Fang¹,Zhu Gangguo¹

Affiliation:

1. Department of Chemistry, Zhejiang Normal University, 688 Yingbin Road, Jinhua 321004, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo301794w

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1. Highly efficient chiral 2-oxazolidinone auxiliaries derived from methylcyclopentadienes and 2-oxazolone

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3. Oxazolone Cycloadducts as Heterocyclic Scaffolds for Alkaloid Construction: Synthesis of (±)-2-epi-Pumiliotoxin C

4. Highly diastereoselective route to trans-5-substituted 2-hydroxymethylpyrrolidine derivatives by radical cyclisation

5. Chemoenzymatic synthesis of the morphine skeleton via radical cyclization and a C10C11 closure

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