Literature DB >> 33870390

Transition metal-free approach to azafluoranthene scaffolds by aldol condensation/[1+2+3] annulation tandem reaction of isocyanoacetates with 8-(alkynyl)-1-naphthaldehydes.

Penghui Dong1, Kashif Majeed, Lingna Wang, Zijian Guo, Fengtao Zhou, Qiuyu Zhang.   

Abstract

A transition metal-free aldol condensation/[1+2+3] annulation reaction of isocyanoacetates with 8-(alkynyl)-1-naphthaldehydes has been developed for the general synthesis of azafluoranthenes. This domino reaction enables successive formation of three new bonds and two rings from readily accessible starting materials in a single operation. Furthermore, this methodology can also be utilized to construct chromeno[4,3-c]pyridines and benzo[c][2,6]naphthyridines in moderate yields.

Entities:  

Year:  2021        PMID: 33870390     DOI: 10.1039/d1cc01015h

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Rapid Access to Hydroxyfluoranthenes via a Domino Suzuki-Miyaura/Intramolecular Diels-Alder/Ring-Opening Reactions Sequence.

Authors:  Dilgam Ahmadli; Yesim Sahin; Eylul Calikyilmaz; Onur Şahin; Yunus E Türkmen
Journal:  J Org Chem       Date:  2022-04-07       Impact factor: 4.198

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.