Literature DB >> 22593036

A mild benzannulation through directed cycloaddition reactions.

James D Kirkham1, Roger J Butlin, Joseph P A Harrity.   

Abstract

Simple as ABC: Alkynyl borane cycloadditions can be substrate-directed to assemble aromatic difluoroboranes within an extremely mild and efficient reaction manifold compared to that of traditional methods (see scheme). The aromatic boranes are readily transformed into a range of useful products.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 22593036     DOI: 10.1002/anie.201200917

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  5 in total

Review 1.  Synthesis of polysubstituted arenes through organocatalytic benzannulation.

Authors:  Qian Zhao; Cheng Peng; Gu Zhan; Bo Han
Journal:  RSC Adv       Date:  2020-11-10       Impact factor: 4.036

2.  Direct access to multi-functionalized benzenes via [4 + 2] annulation of α-cyano-β-methylenones and α,β-unsaturated aldehydes.

Authors:  Qianfa Jia; Yunfei Lan; Xin Ye; Yinhe Lin; Qiao Ren
Journal:  RSC Adv       Date:  2020-08-06       Impact factor: 4.036

3.  A Mild and Regioselective Route to Fluoroalkyl Aromatic Compounds via Directed Cycloaddition Reactions.

Authors:  David L Cousins; Yee Hwee Lim; Joseph P A Harrity
Journal:  J Org Chem       Date:  2022-07-08       Impact factor: 4.198

4.  Arylethynyltrifluoroborate Dienophiles for on Demand Activation of IEDDA Reactions.

Authors:  Zbigniew Zawada; Zijian Guo; Bruno L Oliveira; Claudio D Navo; He Li; Pedro M S D Cal; Francisco Corzana; Gonzalo Jiménez-Osés; Gonçalo J L Bernardes
Journal:  Bioconjug Chem       Date:  2021-07-15       Impact factor: 4.774

5.  Lewis base directed cycloaddition reactions of 2-pyrones and alkynylaluminum reagents.

Authors:  Damien F Crépin; Joseph P A Harrity
Journal:  Org Lett       Date:  2013-08-05       Impact factor: 6.005

  5 in total

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