Double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Kinetic lactonization of 4,6-dimethyl- and 2,4,6,8-tetramethyl-5-hydroxyazelaic acids: ground state conformational control
2. Diastereotopic selectivity at prochiral carbon centers: functionalization of differentiated hydroxymethyl groups provides access to either stereoisomeric configuration
3. Double diastereoselection in the iodolactonization of 1,6-heptadiene-4-carboxylic acids
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1. Intramolecular [3 + 2] Cycloaddition Reactions of Unsaturated Nitrile Oxides. A Study from the Perspective of Bond Evolution Theory (BET);The Journal of Physical Chemistry A;2018-08-24
2. WITHDRAWN: One-pot three-component synthesis of pyrano[3,2-d]isoxazoles catalyzed by N,N,N,N-tetramethylguanidinium formate [TMG][HCO2] as mild basic ionic liquid under mild conditions;Tetrahedron;2013-08
3. Oxidative tandem alkoxide conjugate addition to nitroalkenes/radical 5-exo cyclizations—a versatile synthesis of functionalized 3-nitrotetrahydrofurans;Tetrahedron;2012-02
4. A Straightforward Approach towards Isoxazoline Amino Acid Esters by Domino Michael Additions/Nitrile Oxide Cycloadditions;European Journal of Organic Chemistry;2011-05-18
5. ChemInform Abstract: Double Diastereoselectivity in the Intramolecular Nitrile Oxide-Olefin Cycloaddition (INOC) Reaction.;ChemInform;2010-08-22
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