Further Utilization of Mucohalic Acids: Palladium-Free, Regioselective Etherification and Amination of α,β-Dihalo γ-Methoxycarbonyloxy and γ-Acetoxy Butenolides-Reference-Cited by-同舟云学术

Further Utilization of Mucohalic Acids: Palladium-Free, Regioselective Etherification and Amination of α,β-Dihalo γ-Methoxycarbonyloxy and γ-Acetoxy Butenolides

Published:2003-12-01 Issue:26 Volume:5 Page:5015-5017
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Blazecka Peter G.¹,Belmont Daniel¹,Curran Tim¹,Pflum Derek¹,Zhang Ji¹

Affiliation:

1. Chemical Research and Development, Pfizer Global Research & Development, Ann Arbor Laboratories, Pfizer, Inc., 2800 Plymouth Road, Ann Arbor, Michigan 48105

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol035994n

Reference26 articles.

1. Organic syntheses by means of noble metal compounds XVII. Reaction of π-allylpalladium chloride with nucleophiles

2. (a) Trost, B. M.; Lee, C. InCatalytic Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; Wiley-VCH: New York, 2000; pp 593−649.

3. New synthetic reactions of allyl alkyl carbonates, allyl .beta.-keto carboxylates, and allyl vinylic carbonates catalyzed by palladium complexes

4. New rules of selectivity: allylic alkylations catalyzed by palladium

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