Dibenzofuran Synthesis: Decarbonylative Intramolecular C−H Arylation of Aromatic Esters-Reference-Cited by-同舟云学术

Dibenzofuran Synthesis: Decarbonylative Intramolecular C−H Arylation of Aromatic Esters

Published:2018-06-06 Issue:7 Volume:7 Page:1358-1361
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Okita Toshimasa¹^ORCID,Komatsuda Masaaki¹,Saito Ami N.¹,Hisada Tomoya¹,Takahara Tomoaki T.¹,Nakayama Keito P.¹,Isshiki Ryota¹,Takise Ryosuke²,Muto Kei¹^ORCID,Yamaguchi Junichiro¹^ORCID

Affiliation:

1. Department of Applied Chemistry; Waseda University, 3-4-1 Ohkubo; Shinjuku Tokyo 169-8555 Japan

2. Graduate School of Science; Nagoya University; Chikusa Nagoya 464-8602 Japan

Publisher

Wiley

Subject

Organic Chemistry

Reference60 articles.

1. Potent and Selective Structure-Based Dibenzofuran Inhibitors of Transthyretin Amyloidogenesis: Kinetic Stabilization of the Native State

2. Novel CDK inhibition profiles of structurally varied 1-aza-9-oxafluorenes

3. Psoralen analogues: synthesis, inhibitory activity of growth of human tumor cell lines and computational studies

4. Improved Synthesis of the Two-Photon Caging Group 3-Nitro-2-Ethyldibenzofuran and Its Application to a Caged Thymidine Phosphoramidite

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