A Domino Strategy for the Synthesis of 2H -Pyrans from Propargyl Vinyl Ethers-Reference-Cited by-同舟云学术

A Domino Strategy for the Synthesis of 2H -Pyrans from Propargyl Vinyl Ethers

Published:2019-02-11 Issue:8 Volume:2019 Page:1784-1790
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Tejedor David¹^ORCID,Delgado-Hernández Samuel¹²,Diana-Rivero Raquel¹²,Díaz-Díaz Abián¹²,García-Tellado Fernando¹^ORCID

Affiliation:

1. Instituto de Productos Naturales y Agrobiología; Consejo Superior de Investigaciones Científicas, Astrofísico Francisco Sánchez 3, 38206 La Laguna, Tenerife; Spain

2. Doctoral and Postgraduate School; Universidad de La Laguna; Spain

Funder

Ministerio de Economía, Industria y Competitividad, Gobierno de España

European Regional Development Fund

Canarian Agency for Research, Innovation and the Information Society

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201801847/fullpdf

Reference43 articles.

1. Preparation of Substituted 2H-Pyrans via a Cascade Reaction from Methyl Coumalate and Activated Methylene Nucleophiles

2. Amine-Catalyzed Asymmetric (3 + 3) Annulations of β′-Acetoxy Allenoates: Enantioselective Synthesis of 4H-Pyrans

3. DABCO-catalyzed synthesis of 3-bromo-/3-iodo-2H-pyrans from propargyl alcohols, dialkyl acetylene dicarboxylates, and N-bromo-/N-iodosuccinimides

4. No Acid Required: 4π and 6π Electrocyclization Reactions of Dienyl Diketones for the Synthesis of Cyclopentenones and 2H-Pyrans

5. Sequential Catalyst Phosphine/Secondary Amine Promoted [1+4]/Rearrangement Domino Reaction for the Construction of (2H)-Pyrans and 2-Oxabicyclo[2.2.2]oct-5-ene Skeletons

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