Rh(I)-Catalyzed Transformation of Propargyl Vinyl Ethers into (E,Z)-Dienals: Stereoelectronic Role of trans Effect in a Metal-Mediated Pericyclic Process and a Shift from Homogeneous to Heterogeneous Catalysis During a One-Pot Reaction-Reference-Cited by-同舟云学术

Rh(I)-Catalyzed Transformation of Propargyl Vinyl Ethers into (E,Z)-Dienals: Stereoelectronic Role of trans Effect in a Metal-Mediated Pericyclic Process and a Shift from Homogeneous to Heterogeneous Catalysis During a One-Pot Reaction

Published:2013-12-13 Issue:1 Volume:79 Page:352-364
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Vidhani Dinesh V.¹,Krafft Marie E.¹,Alabugin Igor V.¹

Affiliation:

1. Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306, United States

Funder

National Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo402505f

Reference149 articles.

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2. Acid catalysis of the Claisen rearrangement. 2. Formation of the benzofurobenzopyran and benzofuro[3,2-b]benzofuran skeletons from 1,4-bis(aryloxy)-2-butynes

3. Regioselective Synthesis of Coumarin‐Annulated Polyheterocycles by [3,3] Sigmatropic Rearrangement

4. Regioselective synthesis of pentacyclic polyheterocycles: Sequential [3,3] sigmatropic rearrangement of 4-(4′-aryloxybut-2′-ynyloxy)-1-phenyl-1,8-naphthyridin-2(1H)-ones

5. Regioselective synthesis of biologically interesting pentacyclic polyheterocycles by sequential thio-Claisen and AlCl3 catalyzed oxy-Claisen rearrangement of 4-(4′-aryloxybut-2′-ynylthio)-1-phenyl-1,8-naphthyridin-2(1H)-one

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