N-PROTONATED AZOMETHINE YLIDES WITH A LEAVING GROUP AS SYNTHETIC EQUIVALENTS FOR NONSTABILIZED NITRILE YLIDES
- 5 September 1985
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 14 (9), 1411-1414
- https://doi.org/10.1246/cl.1985.1411
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Generation of azomethine ylides via the desilylation reaction of immonium saltsThe Journal of Organic Chemistry, 1984
- One-pot synthesis of N-[(trimethylsilyl)methyl]imines and (trimethylsilyl)methyl-substituted heterocumulenes from (trimethylsilyl)methyl azideThe Journal of Organic Chemistry, 1984
- 1,3-Dipolar cycloaddition leading to N-alkylpyrrolidines.CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
- Thioimidate methylides by the desilylation method: an improved synthesis of pyrrolines and pyrrolesThe Journal of Organic Chemistry, 1983
- An expedient synthetic approach to the physostigmine alkaloids via intramolecular formamidine ylide cycloadditionsThe Journal of Organic Chemistry, 1983
- 1,3-Dipolar cycloaddition leading to N-acylated pyrrolidines and 2,5-dihydropyrroles.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- A new trimethylsilyl triflate-catalyzed 1,3-dipolar cycloaddition leading to pyrrolidinesTetrahedron Letters, 1982
- Stereospecific synthesis of retronecine by imidate methylide cycloadditionJournal of the American Chemical Society, 1980
- Photochemische Cycloadditionen von 3‐phenyl‐2h‐azirinen mit Aldehyden. 31. Mitteilung über PhotoreaktionenHelvetica Chimica Acta, 1973
- Photochemical transformations of small ring heterocyclic compounds. XLV. Photocycloaddition and photodimerization reactions of arylazirinesThe Journal of Organic Chemistry, 1973