4.8 Article

Enantioselective Nickel-Catalyzed anti-Carbometallative Cyclizations of Alkynyl Electrophiles Enabled by Reversible Alkenylnickel E/Z Isomerization

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 138, Issue 26, Pages 8068-8071

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b04206

Keywords

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Funding

  1. ERC [258580]
  2. EPSRC [EP/I004769/1, EP/I004769/2]
  3. University of Nottingham
  4. GlaxoSmithKline
  5. EPSRC [EP/I004769/2, EP/I004769/1] Funding Source: UKRI
  6. Engineering and Physical Sciences Research Council [EP/I004769/1, EP/I004769/2, 1498235] Funding Source: researchfish

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Nickel-catalyzed additions of arylboronic acids to alkynes, followed by enantioselective cyclizations of the alkenylnickel species onto tethered ketones or enones, are reported. These reactions are reliant upon the formal anti-carbonickelation of the alkyne, which is postulated to occur by the reversible E/Z isomerization of an alkenylnickel species.

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