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Cyclopropenes in Metallacycle-Mediated Cross-Coupling with Alkynes: Convergent Synthesis of Highly Substituted Vinylcyclopropanes.
O'Rourke, Natasha F; Micalizio, Glenn C.
Affiliation
  • O'Rourke NF; Department of Chemistry, Burke Laboratory, Dartmouth College , Hanover, New Hampshire 03755, United States.
  • Micalizio GC; Department of Chemistry, Burke Laboratory, Dartmouth College , Hanover, New Hampshire 03755, United States.
Org Lett ; 18(6): 1250-3, 2016 Mar 18.
Article in En | MEDLINE | ID: mdl-26987882
ABSTRACT
Stereodivergent metallacycle-mediated cross-coupling reactions are described for the synthesis of densely functionalized vinylcyclopropanes from the union of alkynes with cyclopropenes. Strategies explored include hydroxyl-directed and nondirected processes, with the latter of these delivering vinylcyclopropanes with exquisite levels of regio- and stereoselectivity. Challenges inherent to these coupling reactions include diastereoselectivity (with respect to the cyclopropene) and regioselectivity (with respect to both coupling partners).
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Vinyl Compounds / Cyclopropanes / Alkynes Language: En Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Vinyl Compounds / Cyclopropanes / Alkynes Language: En Year: 2016 Type: Article