Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B<sub>2</sub>(dan)<sub>2</sub>)

The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B<sub>2</sub>(dan)<sub>2</sub>) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-10-25
DOI
https://doi.org/10.1021/acs.joc.4c01939
Citations
3
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.75
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article

Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B2(dan)2)

Taiga Yasuda, Shinichi Saito, Yusuke Yoshigoe, Yuki Ito et al.
3 citations
The Journal of Organic Chemistry
Organoboron and organosilicon chemistry
0.75
article

Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B2(dan)2)

Taiga Yasuda, Shinichi Saito, Yusuke Yoshigoe, Yuki Ito, Yuma Koizumi
article en
3 citations

Abstract

The diboration of alkynes by 1,8-diaminonaphthalene-protected diboronic acid (B<sub>2</sub>(dan)<sub>2</sub>) proceeded smoothly in the presence of a platinum catalyst, and 1,2-diborylalkenes were isolated in up to 94% yield. The use of an appropriate solvent and ligand was critical for the progress of the reaction. The derivatization of 1,2-diborylalkenes was briefly examined.

The Journal of Organic ChemistryVol. 89(22)
Tokyo University of Science (JP)
Clean water and sanitation
Openalex Percentile: Top 32%
Organoboron and organosilicon chemistry
0.75
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Platinum-Catalyzed Diboration of Alkynes by 1,8-Diaminonaphthalene-Protected Diboronic Acid (B<sub>2</sub>(dan)<sub>2</sub>) — Taiga Yasuda, Shinichi Saito, et al. · The Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS