Eu(fod)3-Catalyzed Rearrangement of Allylic Methoxyacetates-Reference-Cited by-同舟云学术

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Eu(fod)3-Catalyzed Rearrangement of Allylic Methoxyacetates

Published:1996-01-01 Issue:46 Volume:118 Page:11690-11691
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Shull Brian K.¹,Sakai Takashi¹,Koreeda Masato¹

Affiliation:

1. Department of Chemistry, The University of Michigan Ann Arbor, Michigan 48109-1055

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja962718d

Reference20 articles.

1. (b) Wipf, P. ref 1a; pp. 827−873.

2. (c) Ziegler, F. E. in ref 1a; pp 875−898.

3. Chemistry and stereochemistry of the ion pair derived from trans-5-cyclodecen-1-yl p-nitrobenzoate

4. Stereochemistry of allylic rearrangements. XV. Ion-pair return associated with the solvolysis of trans-.alpha.-methyl-.gamma.-phenylallyl-p-nitrobenzoate in aqueous acetone

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2. Palladium(0)‐Catalyzed Rearrangement of Allylic Esters;ChemistrySelect;2020-02-26

3. Quinine-Promoted, Enantioselective Boron-Tethered Diels–Alder Reaction by Anomeric Control of Transition-State Conformation;The Journal of Organic Chemistry;2018-05-01

4. Formation of Nitriles, Carboxylic Acids, and Derivatives by Rearrangements;Comprehensive Organic Transformations;2018-02-28

5. Palladium-catalysed alkene chain-running isomerization;Chemical Communications;2017

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