Lewis Acid Promoted Hetero [2 + 2] Cycloaddition Reactions of Aldehydes with 10-Propynyl-9(10H)-acridone. A Highly Stereoselective Synthesis of Acrylic Acid Derivatives and 1,3-Dienes Using an Electron Deficient Variant of Ynamine-Reference-Cited by-同舟云学术

Lewis Acid Promoted Hetero [2 + 2] Cycloaddition Reactions of Aldehydes with 10-Propynyl-9(10H)-acridone. A Highly Stereoselective Synthesis of Acrylic Acid Derivatives and 1,3-Dienes Using an Electron Deficient Variant of Ynamine

Published:1999-09-18 Issue:8 Volume:1 Page:1237-1240
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hsung Richard P.¹,Zificsak Craig A.¹,Wei Lin-Li¹,Douglas Christopher J.¹,Xiong Hui¹,Mulder Jason A.¹

Affiliation:

1. Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol990211c

Reference22 articles.

1. UMN Undergraduate Research Participant: 1998−1999. The recipient of 1998 Pharmacia-Upjohn and UMN Department of Chemistry Lando/NSF Program for Summer Research Fellowship.

2. Inverse demand [4+2] cycloaddition reactions of allenamides: Reactivity scopes of an electron deficient variant of allenamines

3. First Stereoselective [4 + 2] Cycloaddition Reactions of 3-Cyanochromone Derivatives with Electron-Rich Dienes: An Approach to the ABC Tricyclic Frame of Arisugacin1

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