Synthesis of sterically hindered 4,5-diarylphenanthrenes via acid-catalyzed bisannulation of benzenediacetaldehydes with alkynes-Reference-Cited by-同舟云学术

Synthesis of sterically hindered 4,5-diarylphenanthrenes via acid-catalyzed bisannulation of benzenediacetaldehydes with alkynes

Published:2019 Issue:21 Volume:10 Page:5470-5475
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Li Yuanming¹²³⁴^ORCID,Yagi Akiko¹²³⁴⁵,Itami Kenichiro¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Transformative Bio-Molecules (WPI-ITbM)

2. Nagoya University

3. Nagoya 464-8602

4. Japan

5. Graduate School of Science

Abstract

Acid-catalyzed bisannulation of benzenediacetaldehydes with alkynes provided a rapid access to sterically hindered 4,5-diarylphenanthrenes and multisubstituted phenanthrenes regioselectively.

Funder

Japan Science and Technology Corporation

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/SC/C9SC00334G

Reference51 articles.

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4. Antimalarial arylaminopropanols

5. C8c–C15 monoseco-analogues of the phenanthroquinolizidine alkaloids julandine and cryptopleurine exhibiting potent anti-angiogenic properties

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