Scandium-Catalyzed Propargylation of 1,3-Diketones with Propargyl Alcohols Bearing Sulfur or Selenium Functional Groups: Useful Transformation to Furans and Pyrans-Reference-Cited by-同舟云学术

Scandium-Catalyzed Propargylation of 1,3-Diketones with Propargyl Alcohols Bearing Sulfur or Selenium Functional Groups: Useful Transformation to Furans and Pyrans

Published:2010 Issue:9 Volume:58 Page:1180-1186
ISSN:0009-2363
Container-title:Chemical and Pharmaceutical Bulletin
language:en
Short-container-title:CHEMICAL & PHARMACEUTICAL BULLETIN

Author:

Ohta Katsuki¹,Kobayashi Taira¹,Tanabe Genzoh²,Muraoka Osamu²,Yoshimatsu Mitsuhiro¹

Affiliation:

1. Department of Chemistry, Faculty of Education, Gifu University

2. School of Pharmacy, Kinki University

Publisher

Pharmaceutical Society of Japan

Subject

Drug Discovery,General Chemistry,General Medicine

Link

http://www.jstage.jst.go.jp/article/cpb/58/9/58_9_1180/_pdf

Reference48 articles.

1. Developments in Furan Syntheses

2. FeCl3-Catalyzed Nucleophilic Substitution of Propargylic Acetates with Enoxysilanes

3. An Easy Route to Acylfurans and Dihydrofurans by Intramolecular Cyclization of Substituted 1,3-Diketones

4. Yb(OTf)3-catalyzed propargylation and allenylation of 1,3-dicarbonyl derivatives with propargylic alcohols: one-pot synthesis of multi-substituted furocoumarin

5. Brønsted Acid Mediated Heterogeneous Addition Reaction of 1,3-Dicarbonyl Compounds to Alkenes and Alcohols

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