✦ LIBER ✦

Nucleophilic substitution reaction of 2,6-difluorobenzonitrile

✍ Scribed by Yong-da Lin; Zhang-ting Li; Ching-sung Chi

Publisher: Elsevier Science
Year: 1991
Tongue: English
Weight: 38 KB
Volume: 54
Category: Article
ISSN: 0022-1139
DOI: 10.1016/s0022-1139(00)83614-3

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

2,6-Difluorobenzonitrile

✍ Britton, Doyle 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 173 KB

Microwave Spectrum of 2,6-Difluorobenzon

Microwave Spectrum of 2,6-Difluorobenzonitrile

✍ S.D. Sharma; S. Doraiswamy 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 204 KB

The molecule 2,6-difluorobenzonitrile has been analyzed in the frequency ranges from 8 to 12 GHz and from 31 to 40 GHz at dry ice temperature using a conventional 100 kHz and a Hewlett-Packard 33 kHz Stark-modulated microwave spectrometer, respectively. The rotational and centrifugal distortion cons

Preparation of 6-fluorobenzisothiazoles

Preparation of 6-fluorobenzisothiazoles via a regioselective nucleophilic aromatic substitution reaction

✍ David M. Fink; Joseph T. Strupczewski 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 232 KB

An unusual nucleophilic aromatic substit

An unusual nucleophilic aromatic substitution reaction

✍ Kenneth B. Tomer; Agneta Weisz 📂 Article 📅 1976 🏛 Elsevier Science 🌐 French ⚖ 105 KB

Highly Regioselective DABCO-Catalyzed Nu

Highly Regioselective DABCO-Catalyzed Nucleophilic Aromatic Substitution (SNAr) Reaction of Methyl 2,6-Dichloronicotinate with Phenols.

✍ Yao-Jun Shi; Guy Humphrey; Peter E. Maligres; Robert A. Reamer; J. Michael Willi 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 20 KB 👁 1 views

Highly Regioselective DABCO-Catalyzed Nu

Highly Regioselective DABCO-Catalyzed Nucleophilic Aromatic Substitution (SNAr) Reaction of Methyl 2,6-Dichloronicotinate with Phenols

✍ Yao-Jun Shi; Guy Humphrey; Peter E. Maligres; Robert A. Reamer; J. Michael Willi 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 78 KB

## Abstract Exclusive formation of 6‐aryloxy ethers **9** from an S~N~Ar reaction of methyl 2,6‐dichloronicotinate (**2**) with phenols **7** catalyzed by 1,4‐diazabicyclo[2.2.2]octane (DABCO) in the presence of stoichiometric triethylamine is described. The reaction proceeds __via__ the regioselec