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J Am Chem Soc. 2009 Nov 18;131(45):16525-8. doi: 10.1021/ja906480w.

C-H bond functionalization via hydride transfer: direct coupling of unactivated alkynes and sp(3) C-H bonds catalyzed by platinum tetraiodide.

Author information

1
Department of Chemistry, Columbia University, 3000 Broadway, New York, New York 10027, USA.

Abstract

We report a catalytic intramolecular coupling between terminal unactivated alkynes and sp(3) C-H bonds via through-space hydride transfer (HT-cyclization of alkynes). This method enables one-step preparation of complex heterocyclic compounds by alpha-alkenylation of readily available cyclic ethers and amines. We show that PtI(4) is an effective Lewis acid catalyst for the activation of terminal alkynes for hydride attack and subsequent C-C bond formation. In addition, we have shown that the activity of neutral platinum salts (PtX(n)) can be modulated by the halide ligands. This modulation in turn allows for fine-tuning of the platinum center reactivity to match the reactivity and stability of selected substrates and products.

PMID:
19852462
PMCID:
PMC2971677
DOI:
10.1021/ja906480w
[Indexed for MEDLINE]
Free PMC Article

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