Copper-catalysed enantioselective intramolecular etherification of propargylic esters: synthetic approach to chiral isochromans-Reference-Cited by-同舟云学术

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Copper-catalysed enantioselective intramolecular etherification of propargylic esters: synthetic approach to chiral isochromans

Published:2019 Issue:33 Volume:9 Page:18918-18922
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Liu Shiyao¹²³⁴⁵,Nakajima Kazunari⁶²³⁴⁵^ORCID,Nishibayashi Yoshiaki¹²³⁴⁵^ORCID

Affiliation:

1. Department of Systems Innovation

2. School of Engineering

3. The University of Tokyo

4. Bunkyo-ku

5. Japan

6. Frontier Research Centre for Energy and Resources

Abstract

The first example for direct synthesis of chiral terminal alkynyl isochromans.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Science and Technology Agency

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/RA/C9RA03880A

Reference40 articles.

1. Isochroman structures in lignin: a new β-1 pathway

2. A New Antifungal Metabolite from Penicillium expansum

3. (1R,3S)-1-(Aminomethyl)-3,4-dihydro-5,6-dihydroxy-3-phenyl-1H-2-benzopyran: a potent and selective D1 agonist

4. Furo[3,2-h]isochroman, furo[3,2-h]isoquinoline, isochroman, phenol, pyranone, and pyrone derivatives from the sea fan-derived fungus Penicillium sp. PSU-F40

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