Gold(i)-catalyzed Nicholas reaction with aromatic molecules utilizing a bifunctional propargyl dicobalt hexacarbonyl complex-Reference-Cited by-同舟云学术

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Gold(i)-catalyzed Nicholas reaction with aromatic molecules utilizing a bifunctional propargyl dicobalt hexacarbonyl complex

Published:2019 Issue:37 Volume:17 Page:8522-8526
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Okamura Toshitaka¹²³⁴,Fujiki Shogo¹²³⁴,Iwabuchi Yoshiharu¹²³⁴^ORCID,Kanoh Naoki¹²³⁴⁵^ORCID

Affiliation:

1. Graduate School of Pharmaceutical Sciences

2. Tohoku University

3. Sendai 980-8578

4. Japan

5. Institute of Medicinal Chemistry

Abstract

A benchtop-stable reagent for the catalytic Nicholas reaction with aromatic molecules was developed.

Funder

Naito Foundation

Ministry of Education, Culture, Sports, Science and Technology

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB01348B

Reference36 articles.

1. The growing applications of click chemistry

2. The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview

3. Statistical Investigation into the Structural Complementarity of Natural Products and Synthetic Compounds

4. GaCl3-Catalyzed Ortho-Ethynylation of Phenols

5. Gold-Catalyzed Ethynylation of Arenes

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1. Nicholas Reaction;Patai's Chemistry of Functional Groups;2023-10-18

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3. Cycloisomerization of π‐Coupled Heteroatom Nucleophiles by Gold Catalysis: En Route to Regiochemically Defined Heterocycles;The Chemical Record;2021-06

4. Gold-Catalyzed Amide/Carbamate-Linked N,O-Acetal Formation with Bulky Amides and Alcohols;The Journal of Organic Chemistry;2020-12-22

5. Highly Chemoselective gem ‐Difluoropropargylation of Aliphatic Alcohols;Chemistry – A European Journal;2019-11-12

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