Facile Synthesis of 1,1′-Binaphthyl-2-carboxylates via Nucleophilic Aromatic Substitution of 1-Methoxy-2-naphthoic Esters by 1-Naphthyl Grignard Reagents-Reference-Cited by-同舟云学术

Facile Synthesis of 1,1′-Binaphthyl-2-carboxylates via Nucleophilic Aromatic Substitution of 1-Methoxy-2-naphthoic Esters by 1-Naphthyl Grignard Reagents

Published:1990-01 Issue:1 Volume:19 Page:143-144
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Hotta Hiroki,Suzuki Takatsugu,Miyano Sotaro

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/19/1/19_1_143/_pdf

Reference9 articles.

1. Preparation and application of axially chiral biaryls to asymmetric reactions.

2. Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-transition-metal complexes. 6. Practical asymmetric synthesis of 1,1'-binaphthyls via asymmetric cross-coupling with a chiral [(alkoxyalkyl)ferrocenyl]monophosphine/nickel catalyst

3. Optical Resolution of 2′-Methoxy-1,1′-binaphthyl-2-carboxylic Acid, and Application to Chiral Derivatizing Agent for HPLC Separation of Enantiomeric Alcohols and Amines

4. Use of Axially Chiral 2′-Methoxy-1,1′-binaphthyl-2-carboxylic Acid as Chiral Derivatizing Agent for Discrimination of Enantiomeric Alcohols and Amines by1H NMR

5. Practical Synthesis of 1,1′-Binaphthyl-2-carboxylic Acids via Side Chain Oxidation of 2-Methyl-1,1′-binaphthyls

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