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Journal ArticleDOI

Oxazolines. XI. Synthesis of functionalized aromatic and aliphatic acids. Useful protecting group for carboxylic acids against Grignard and hydride reagents

Albert I. Meyers, +3 more
- 01 Sep 1974 - 
- Vol. 39, Iss: 18, pp 2787-2793
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This article is published in Journal of Organic Chemistry.The article was published on 1974-09-01. It has received 161 citations till now. The article focuses on the topics: Protecting group & Hydride.

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Phosphinoaryl- and phosphinoalkyloxazolines as new chiral ligands for enantioselective catalysis: Very high enantioselectivity in palladium catalyzed allylic substitutions

TL;DR: Chiral phosphinoaryl-and phosphinoalkyloxazolines, a new class of chelate ligands, were prepared via convenient routes as mentioned in this paper, and Palladium complexes of the new ligands have proved to be highly effective catalysts for allylic substitution reactions.
Patent

Substituted 2-anilinopyrimidines useful as protein kinase inhibitors

TL;DR: The src-family protein kinase inhibitors as mentioned in this paper are selective inhibitors of protein kinases, and are of use in the prophylaxis and treatment of immune diseases, hyperproliferative disorders and other diseases in which inappropriate kinase action is believed to have a role.
Journal ArticleDOI

Recent developments in methods for the esterification and protection of the carboxyl group

TL;DR: Some of the more recent innovations and techniques which have been developed in the past 10-15 years around these features of carboxyl group chemistry are discussed in this article, with a review.
Journal ArticleDOI

Sulfonyl‐1,2,3‐Triazoles: Convenient Synthones for Heterocyclic Compounds

TL;DR: It is reported that Rh–azavinyl carbenes react with aldehydes to give adducts that undergo an intramolecular cyclization instead of a 1,3-dipolar cycloaddition, which results in homochiral 3-sulfonyl-4-oxazolines 4, which are produced in excellent yield and with high enantioselectivity.
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