Diborylation of Alkynyl MIDA Boronates and Sequential Chemoselective Suzuki–Miyaura Couplings: A Formal Carboborylation of Alkynes-Reference-Cited by-同舟云学术

Diborylation of Alkynyl MIDA Boronates and Sequential Chemoselective Suzuki–Miyaura Couplings: A Formal Carboborylation of Alkynes

Published:2013-12-23 Issue:2 Volume:16 Page:440-443
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hyodo Keita¹,Suetsugu Masato¹,Nishihara Yasushi¹²

Affiliation:

1. Division of Earth, Life, and Molecular Sciences, Graduate School of Nature Science and Technology, Okayama University, 3-1-1 Tsushimanaka, Kita-ku, Okayama 700-8530, Japan

2. Japan Science and Technology Agency, ACT-C, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol403326z

Reference65 articles.

1. Diboron Tetrachloride, B2Cl4, as a Reagent for the Synthesis of Organo-boron Compounds. I. The Reaction of Diboron Tetrachloride with Ethylene1

2. Chemistry of Group 13 element-transition metal linkage — the platinum- and palladium-catalyzed reactions of (alkoxo)diborons

3. Metal-catalyzed reactions of diborons for synthesis of organoboron compounds

4. Synthesis and Reactivity of Silylboranes

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