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1,7‐Electrocyclizations of Stabilized Azomethine Ylides.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Nyerges, Miklos +3 more
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Synergistic Catalysis with Azomethine Ylides
Chinese Journal of Chemistry, 2020AbstractAzomethine ylides are useful intermediates for the rapid construction of chiral N‐containing compounds. However, its synthetic potential has not been fully developed due to the limited reaction models. In combination with synergistic catalysis and azomethine ylide chemistry, we have developed several types of novel catalytic system including Cu/
Liang Wei, Chun‐Jiang Wang
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Oxazoline route to azomethine ylides
Journal of the American Chemical Society, 1986Etude de la generation de N-alhylidene ammonioethylenolates a partir d'oxazolines-4; les betaines sont piegees par cycloadditions avec le butynedioate de dimethyle ou l'acrylate de ...
Edwin. Vedejs, Janet Wisniewski. Grissom
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Azomethine Ylides in Organic Synthesis
Current Organic Chemistry, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Carmen Najera, Jose M. Sansano
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Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides
Chemical Reviews, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
Iain, Coldham, Richard, Hufton
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ChemInform Abstract: N‐Metalated Azomethine Ylides
ChemInform, 1993AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
S. KANEMASA, O. TSUGE
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Enantioselective Copper‐Catalyzed [3+3] Cycloaddition of Azomethine Ylides with Azomethine Imines
Angewandte Chemie, 2013Enantioselective copper-catalyzed [3+3] cycloaddition of azomethine ylides with azomethine ...
Hongchao, Guo +12 more
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Enantioselective Cycloadditions of Azomethine Ylides
2008The asymmetric 1,3-DCR of azomethine ylides, which is generated from the corresponding imino ester and alkenes, is one of the most fascinating transformations because the configuration of the four new stereogenic centers of the finally obtained proline can be absolutely established in only one step with total atom economy.
Carmen Nájera, José M. Sansano
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