Ni-Catalyzed regio- and stereoselective addition of arylboronic acids to terminal alkynes with a directing group tether-Reference-Cited by-同舟云学术

Ni-Catalyzed regio- and stereoselective addition of arylboronic acids to terminal alkynes with a directing group tether

Published:2017 Issue:27 Volume:53 Page:3894-3897
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Hari Babu Madala¹²³⁴,Ranjith Kumar Gadi¹²³⁴⁵,Kant Ruchir⁶²³⁴,Sridhar Reddy Maddi¹²³⁴⁵^ORCID

Affiliation:

1. MPC Division

2. CSIR-Central Drug Research Institute

3. Lucknow 226031

4. India

5. Academy of Scientific and Innovative Research

6. MSB Division

Abstract

Addition of arylboronic acids to directing group tethered acetylenes in a regio and stereoselective manner using an inexpensive catalytic system is achieved for the first time to access highly sought after allyl/homoallyl alcohol/amine units.

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/2017/CC/C6CC10256E

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4. Novel One-pot Three-component Coupling Reaction with Trimethylsilylmethyl-phosphonate, Acyl Fluoride, and Aldehyde through the Horner–Wadsworth–Emmons Reaction

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