Literature DB >> 16277337

Arylsulfonate-based nucleophile assisting leaving groups.

Salvatore D Lepore1, Anjan K Bhunia, Pamela Cohn.   

Abstract

[Chemical reaction: See text] The synthesis and unique reactivity of a series of arylsulfonate-based nucleophile assisting leaving groups (NALG) containing oligomeric ether units (including crown ethers) attached to the arylsulfonyl ring in the ortho orientation are described. The reactions of a variety of these ether-containing alkyl sulfonates with metal halides proceeded at substantially greater rates than electronically similar sulfonates. These ether-containing leaving groups also displayed marked selectivity for lithium halides relative to the corresponding sodium and potassium salts in nucleophilic displacement reactions.

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Year:  2005        PMID: 16277337      PMCID: PMC3563673          DOI: 10.1021/jo051241y

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  4 in total

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  4 in total
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1.  Recent advances in heterolytic nucleofugal leaving groups.

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2.  Synthesis of Novel C-Pivot Lariat 18-Crown-6 Ethers and their Efficient Purification.

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3.  Rapid conversion of hindered arylsulfonates to alkyl chlorides with retention of configuration.

Authors:  Salvatore D Lepore; Anjan K Bhunia; Deboprosad Mondal; Pamela C Cohn; Craig Lefkowitz
Journal:  J Org Chem       Date:  2006-04-14       Impact factor: 4.354

4.  Crown Ether Nucleophilic Catalysts (CENCs): Agents for Enhanced Silicon Radiofluorination.

Authors:  Susovan Jana; Mohammed H Al-Huniti; Bo Yeun Yang; Shuiyu Lu; Victor W Pike; Salvatore D Lepore
Journal:  J Org Chem       Date:  2017-02-20       Impact factor: 4.354

5.  Enhanced Nucleophilic Fluorination and Radiofluorination of Organosilanes Appended with Potassium-Chelating Leaving Groups.

Authors:  Mohammed H Al-Huniti; Shuiyu Lu; Victor W Pike; Salvatore D Lepore
Journal:  J Fluor Chem       Date:  2014-02-01       Impact factor: 2.050

6.  Nucleophile assisting leaving groups: a strategy for aliphatic 18F-fluorination.

Authors:  Shuiyu Lu; Salvatore D Lepore; Song Ye Li; Deboprosad Mondal; Pamela C Cohn; Anjan K Bhunia; Victor W Pike
Journal:  J Org Chem       Date:  2009-08-07       Impact factor: 4.354

  6 in total

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