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 well as ethyl 2,6-dihydro-6-(prop-2-ynyl)furo(2,3-c)pyridine-3-carboxylate 6.The

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Control of leaf development in the water fern Ceratopteris richardii by the auxin efflux transporter CrPINMa in the CRISPR/Cas9 analysis

Abstract Background PIN-FORMED genes (PINs) are crucial in plant development as they determine the directionality of auxin flow.They are present in almost all land plants and even in green algae.However, their role DETANGLER in fern development has not yet been determined.This study aims to investigate the function of CrPINMa in the quasi-model wat

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