Results 121 to 130 of about 6,255 (178)

Addition of Azomethine Ylides: Fulleropyrrolidines

ChemInform, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
MAGGINI, MICHELE, MENNA, ENZO
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Azomethine Ylides

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
L. M. Harwood, R. J. Vickers
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Synergistic Catalysis with Azomethine Ylides

Chinese Journal of Chemistry, 2020
AbstractAzomethine 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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1,7‐Electrocyclizations of Stabilized Azomethine Ylides.

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Nyerges, Miklos, Viranyi, Andrea, Pinter, Aron, Toke, Laszlo   +3 more
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Azomethine Ylides in Organic Synthesis

Current Organic Chemistry, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Carmen Najera, Jose M. Sansano
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The azomethine ylide strategy for β-lactam synthesis. An evaluation of alternative pathways for azomethine ylide generation

Journal of the Chemical Society, Perkin Transactions 1, 2001
Following the generation of azomethine ylide 3 from the β-lactam-based oxazolidinone 1, a series of alternative entries to this and related 1,3-dipoles have been explored. The first approach is based on the use of monocyclic azetidinones 6–12 and 14 carrying a leaving group at C(4) and an activated (acidic) proton adjacent to the ring nitrogen ...
Brown, D, Martel, SR, Wisedale, R, Charmant, JPH, Hales, NJ, Fishwick, CWG, Gallagher, TC   +6 more
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Azomethine Ylides

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
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Oxazoline route to azomethine ylides

Journal of the American Chemical Society, 1986
Etude 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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Synthesis and Use of a Trifluoromethylated Azomethine Ylide Precursor

The Journal of Organic Chemistry, 2012
The presence of fluorous substituents can impart a dramatic effect on the efficacy of molecules used for a range of applications in society. Here, we describe the preparation and use of a new trifluoromethylated azomethine ylide precursor, which leads to a series of fluorinated pyrrolidine, 3-pyrroline, and pyrrole building blocks.
Gaël, Tran, Robin, Meier, Lawrence, Harris, Duncan L, Browne, Steven V, Ley   +4 more
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Enantioselective Cycloadditions of Azomethine Ylides

2008
The 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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