Stereoselective Formation of a Chiral Ether by Intramolecular O–H Insertion Reaction of a Metal Carbenoid Generated from Diazoacetoacetate
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference38 articles.
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3. Catalytic Enantioselective O−H Insertion Reactions
4. Enantiopure α-Silyl-Substituted α-Hydroxyacetic Acids Using O-H Insertion Methodology and Boron-Based Asymmetric Reductions
5. .alpha.-Hydroxy esters as chiral auxiliaries in asymmetric cyclopropanations by rhodium(II)-stabilized vinylcarbenoids
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1. Rh2(esp)2: An Efficient Catalyst for O-H Insertion Reactions of Carboxylic Acids into Acceptor/Acceptor Diazo Compounds;European Journal of Organic Chemistry;2016-03-09
2. Regioselective Synthesis of Highly Functionalized Furans Through the RuII-Catalyzed [3+2] Cycloaddition of Diazodicarbonyl Compounds;European Journal of Organic Chemistry;2014-04-17
3. Rhodium(ii) catalyzed synthesis of macrocycles incorporating oxindole via O–H/N–H insertion reactions;Org. Biomol. Chem.;2014
4. Combined C–H functionalization/O–H insertion reaction to form tertiary β-alkoxy substituted β-aminophosphonates catalyzed by [Cu(MeCN)4]PF6;Organic & Biomolecular Chemistry;2013
5. Remote stereocontrol of intramolecular rhodium carbene addition driven by a small and flexible chiral 2,4-pentanediol tether;Tetrahedron;2012-05
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