ULTRASONIC SYNTHESIS, MOLECULAR STRUCTURE AND MECHANISTIC STUDY OF 1,3-DIPOLAR CYCLOADDITION REACTION OF 1-ALKYNYLPYRIDINIUM-3-OLATE AND ACETYLENE DERIVATIVES

Ultrasonic Synthesis, Molecular Structure and Mechanistic Study of 1,3-Dipolar Cycloaddition Reaction of 1-Alkynylpyridinium-3-olate and Acetylene Derivatives

Regioselectively, ethyl propiolate reacted with 1-(propergyl)-pyridinium-3-olate to give two regioisomers; ethyl 4-oxo-8-(prop-2-ynyl)-8-aza-bicyclo(3.2.1)octa-2,6-diene-6-carboxylate 4, ethyl 2-oxo-8-(prop-2-ynyl)-8-aza-bicyclo(3.2.1)octa-3,6-diene-6-carboxylate 5 as Blunt Wraps well as ethyl 2,6-dihydro-6-(prop-2-ynyl)furo(2,3-c)pyridine-3-carbox

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Residuation in orthomodular lattices

We show that every Originals High Rise Loose idempotent weakly divisible residuated lattice satisfying the double negation law can be transformed into an orthomodular lattice.The converse holds if adjointness is replaced by conditional adjointness.Moreover, we show that every positive right residuated lattice satisfying the double negation law and

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