4.8 Article

Unprecedented Synthesis of Alkynylphosphine-boranes through Room-Temperature Oxidative Alkynylation

Journal

ORGANIC LETTERS
Volume 15, Issue 17, Pages 4592-4595

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol402197d

Keywords

-

Funding

  1. Universite Libre de Bruxelles
  2. Universite de Versailles Saint-Quentin-en-Yvelines
  3. CNRS
  4. FNRS [F.4530.13]
  5. Region Basse-Normandie
  6. European Union (FEDER Funds)
  7. COST ACTION [CM0802]
  8. Ministere de la Recherche and the Fonds pour la formation a la Recherche dans l'Industrie et dans l'Agriculture (F.R.I.A.)

Ask authors/readers for more resources

An original and user-friendly synthesis of alkynylphosphine-boranes, useful building blocks in organic synthesis, based on an oxidative P-alkynylation reaction with readily available copper acetylides is reported. The ability of a secondary phosphine protected with a borane to undergo oxidative coupling without oxidation of the P-moiety is demonstrated for the first time. The reaction, which proceeds at room temperature, is applicable to the preparation of enantioenriched and structurally complex alkynylphosphine-boranes.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available