Nickel-catalyzed, ligand-free, diastereoselective synthesis of 3-methyleneindan-1-ols-Reference-Cited by-同舟云学术

Nickel-catalyzed, ligand-free, diastereoselective synthesis of 3-methyleneindan-1-ols

Published:2018 Issue:87 Volume:54 Page:12389-12392
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Panchal Heena¹²³⁴⁵,Clarke Christopher¹²³⁴⁵,Bell Charles¹²³⁴⁵,Karad Somnath Narayan¹²³⁴⁵,Lewis William⁶²⁷⁴⁵^ORCID,Lam Hon Wai¹²³⁴⁵^ORCID

Affiliation:

1. The GlaxoSmithKline Carbon Neutral Laboratories for Sustainable Chemistry

2. University of Nottingham

3. Jubilee Campus

4. Nottingham

5. UK

6. School of Chemistry

7. University Park

Abstract

Nickel-catalyzed, highly diastereoselective annulations between activated allenes and 2-acetylarylboronic acid or 2-formylarylboronic acids to give 3-methyleneindan-1-ols are reported.

Funder

H2020 Marie Skłodowska-Curie Actions

Engineering and Physical Sciences Research Council

University of Nottingham

GlaxoSmithKline

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC06388E

Reference39 articles.

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2. Enantioselective syntheses of indanes: from organocatalysis to C–H functionalization

3. RECENT ADVANCES IN THE SYNTHESIS OF INDAN SYSTEMS. A REVIEW

4. Palladium catalyzed intramolecular nucleophilic addition of allylic species, generated from allene, to aryl aldehydes and ketones

5. Preparation of Alkylidene Indane and Related Scaffolds and Their Further Elaboration to Novel Chemotypes

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