Literature DB >> 31403311

Annulative π-Extension of Unactivated Benzene Derivatives through Nondirected C-H Arylation.

Jae Bin Lee1, Min Ho Jeon1, Jeong Kon Seo2, Gert von Helden3, Jan-Uwe Rohde4, Bum Suk Zhao4, Jongcheol Seo5, Sung You Hong1.   

Abstract

Annulative π-extension chemistry provides a concise synthetic route to polycyclic arenes. Herein, we disclose a nondirected annulation approach of unactivated simple arenes. The palladium-catalyzed 2-fold C-H arylation event facilitates tandem C-C linkage relays to furnish fully benzenoid triphenylene frameworks using cyclic diaryliodonium salts. The inseparable regioisomeric mixture of 1- and 2-methyltriphenylenes is identified by the combined analysis of ion mobility-mass spectrometry, gas-phase infrared spectroscopy, and molecular simulation studies.

Entities:  

Year:  2019        PMID: 31403311     DOI: 10.1021/acs.orglett.9b02583

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Rapid access to polycyclic N-heteroarenes from unactivated, simple azines via a base-promoted Minisci-type annulation.

Authors:  Jae Bin Lee; Gun Ha Kim; Ji Hwan Jeon; Seo Yeong Jeong; Soochan Lee; Jaehyun Park; Doyoung Lee; Youngkook Kwon; Jeong Kon Seo; Joong-Hyun Chun; Seok Ju Kang; Wonyoung Choe; Jan-Uwe Rohde; Sung You Hong
Journal:  Nat Commun       Date:  2022-05-03       Impact factor: 17.694

2.  Small organic molecules with tailored structures: initiators in the transition-metal-free C-H arylation of unactivated arenes.

Authors:  Zhenghui Liu; Peng Wang; Yu Chen; Zhenzhong Yan; Suqing Chen; Wenjun Chen; Tiancheng Mu
Journal:  RSC Adv       Date:  2020-04-09       Impact factor: 4.036

  2 in total

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