Facile Synthesis of 3-Amido-Dienynes via a Tandem α-Propargylation–Isomerization of Chiral Allenamides and their Applications in Diels–Alder Cycloadditions-Reference-Cited by-同舟云学术

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Facile Synthesis of 3-Amido-Dienynes via a Tandem α-Propargylation–Isomerization of Chiral Allenamides and their Applications in Diels–Alder Cycloadditions

Published:2017-09-01 Issue:20 Volume:28 Page:2906-2912
ISSN:0936-5214
Container-title:Synlett
language:en
Short-container-title:Synlett

Author:

Ma Zhi-Xiong¹^ORCID,Fang Li-Chao,Haugen Bryan¹,Bruckbauer Daniel¹,Feltenberger John¹,Hsung Richard¹

Affiliation:

1. Division of Pharmaceutical Sciences, School of Pharmacy, and Department of Chemistry, University of Wisconsin

Abstract

A series of interesting 3-amido-dienynes was synthesized via tandem α-propargylation–isomerization of chiral allenamides with moderate E/Z ratio. Reactivities of E and Z isomers were examined.

Funder

National Institutes of Health

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1590899.pdf

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent Advances in the Synthesis of Propargyl Derivatives, and Their Application as Synthetic Intermediates and Building Blocks;Molecules;2023-04-11

2. Recent progress in transition-metal-free functionalization of allenamides;RSC Advances;2020

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