Acidic isomerization of vicinally substituted (cis)-acceptor-donor cyclopropanes via an open ring mechanism
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Electrophilic cyclopropanes in organic synthesis
2. 1,5-addition of dialkylcuprate reagents to alkylcyclopropyl ketones
3. Electrophile-initiated selective ring transformations of cyclopropyl ketones
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1. ChemInform Abstract: Acidic Isomerization of Vicinally Substituted (cis)-Acceptor-Donor Cyclopropanes via an Open Ring Mechanism.;ChemInform;2010-08-19
2. Easy access to trans-2,3-disubstituted cyclobutanones, 2,4,5-trisubstituted 3,6-dihydro-2H-pyrans and cis-substituted phenylcyclopropylsulfones by using the highly versatile 1-phenylsulfenyl- or 1-phenylsulfonyl-cyclopropylketones;Organic & Biomolecular Chemistry;2009
3. Hormaomycin Analogues by Precursor-Directed Biosynthesis - Synthesis of and Feeding Experiments with Amino Acids Related to the Unique 3-(trans-2-Nitrocyclopropyl)alanine Constituent;European Journal of Organic Chemistry;2005-03
4. Sequenced elimination–reduction and elimination–cyclopropanation reactions of 2,3-epoxyamides promoted by samarium diiodide. Synthesis of 2,3-dideuterioamides and cyclopropanamides;Tetrahedron;2004-10
5. Synthesis of (E)-α-Hydroxy-β,γ-Unsaturated Amides with High Selectivity fromα,β-Epoxyamides by Using Catalytic Samarium Diiodide or Triiodide;Chemistry - A European Journal;2004-05-17
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