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Oxidation. --- Addition reaction --- Alkylation --- Catalysis --- Reduction (chemistry) --- Transition state structure --- Addition reaction --- Alkylation --- Catalysis --- Reduction (chemistry) --- Transition state structure
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Chemical kinetics. --- Epoxy resins --- Isocyanates --- Nuclear magnetic resonance --- Spectroscopic analysis --- Amines --- Addition reaction --- Epoxy resins --- Isocyanates --- Nuclear magnetic resonance --- Spectroscopic analysis --- Amines --- Addition reaction
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Physical organic chemistry --- Chimie organique physique --- Addition reaction --- Cycloaddition reaction --- Elimination reaction --- Spectroscopy
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ASYMMETRIC SYNTHESIS --- HYDROGENATION --- ALKENES --- ISOMERIZATION --- TRANSITION METAL COMPLEXES --- CARBONYL COMPLEXES --- ADDITION REACTION --- PROSTAGLANDINS --- CATALYSIS --- REACTIONS --- PREPARATION --- ASYMMETRIC SYNTHESIS --- HYDROGENATION --- ALKENES --- ISOMERIZATION --- TRANSITION METAL COMPLEXES --- CARBONYL COMPLEXES --- ADDITION REACTION --- PROSTAGLANDINS --- CATALYSIS --- REACTIONS --- PREPARATION
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Descriptive organic chemistry --- Organic compounds --- Synthesis --- Chemistry, Organic. --- Synthesis. --- Hydrogenation. --- Organic compounds. --- Oxidation. --- Organic compounds - Synthesis --- Addition reaction --- Deuteration --- Halogenation --- Rearrangement (chemistry) --- Substitution
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This volume presents exciting new developments in preparative heterocyclic chemistry with a special emphasis on the stereoselective synthesis of - or with the aid of - heterocycles. A wide range of modern methods and strategies for the construction and synthetic elaboration of versatile heterocycles is surveyed in depth by leading researchers in this field. Due to the high quality and up-to-date coverage of each chapter, this volume provides a valuable overview of the different aspects discussed and will at the same time be highly inspiring for the expert synthetic organic chemist as well as the non-specialist reader.
Heterocyclic compounds. --- Stereochemistry. --- Heterocyclic compounds --- Synthesis. --- Chemistry. --- Organic chemistry. --- Organic Chemistry. --- Organic chemistry --- Chemistry --- Heterocyclic compounds - Synthesis. --- HETEROCYCLIC COMPOUNDS --- RING OPENING --- NUCLEOPHILIC ADDITION REACTION --- CHIRAL SYNTHONS --- STEREOSELECTIVE SYNTHESIS (NATURAL PRODUCTS CHEMISTRY) --- PREPARATION
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Chemical reactions. --- Chemistry, Organic. --- Solution (Chemistry) --- Basic Sciences. Chemistry --- Organic Chemistry --- Solution (Chemistry). --- Organic Chemistry. --- ORGANIC COMPOUNDS --- SOLUTIONS --- WATER --- ORGANOMETALLIC COMPOUNDS --- CYCLOADDITION REACTION --- NUCLEOPHILIC ADDITION REACTION --- OXIDATION --- REDUCTION --- REACTIONS --- PROPERTIES
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fysicochemie --- Organic reaction mechanisms and kinetics --- Addition reactions --- Ring formation (Chemistry) --- Stereochemistry --- #WSCH:LOSH --- 541.124:547 --- 541.124:547 Chemical dynamics in general. Reaction mechanism in general-:-Organic chemistry --- 541.124:547 Limits of reactions-:-Organic chemistry --- Chemical dynamics in general. Reaction mechanism in general-:-Organic chemistry --- Limits of reactions-:-Organic chemistry --- Atoms --- Molecular asymmetry --- Chemical structure --- Chemistry --- Isomerism --- Polarization (Light) --- Cyclization (Chemistry) --- Cycloaddition --- Exo-condensation --- Chemical reactions --- Space arrangement --- Organic cyclic compounds --- Cycloaddition reaction --- Ene addition reaction --- Rearrangement (chemistry)
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This Special Issue on carboranes is dedicated to Prof. Alan Welch on the occasion of his retirement and his outstanding contributions to the field of carborane chemistry. Polyhedral carboranes lie at the interface of organic and inorganic chemistry. One of their most attractive and important features is the variety and beauty of their chemical structures. They have found applications as diverse as catalysis, in Boron Neutron Capture Therapy, as liquid crystals and as semiconductors. This Special Issue illustrates the very comprehensive world of heteroborane chemistry, from liquid crystals to BNCT agents, di-halogen bonding to quantum chemical calculations of tetrel complexes of the carbonium ylide CB11H11, nickellacarboranes as potential acid–base sensors to revealing how the selective formations of metallacarborane diastereomers can arise and metallacarboranes as function as radical cation salts with dielectric or semiconductor properties.
Research & information: general --- carboranes --- DFT --- reaction pathways --- boron chemistry --- o-carborane --- sulfa-Michael addition reaction --- cysteine --- boron neutron capture therapy --- o-carborane decapitation --- labeled compound --- 1,1′-bis(o-carborane) --- deboronation --- metalation --- bis(nickelation) --- diastereoisomers --- stereospecific --- boron clusters --- liquid crystals --- fluorescence --- cholesterol --- nido-carborane --- nitrilium derivatives --- nickel(II) half-sandwich complexes --- synthesis --- structure --- Lewis acid --- carborane --- carbonium ylide --- tetrel bond --- quantum chemistry --- electron density --- ELF --- iodo derivatives --- dihalogen bond --- X-ray structure --- quantum chemical calculations --- iron bis(1,2-dicarbollide) --- chromium bis(1,2-dicarbollide) --- tetramethyltetrathiafulvalene --- tetramethyltetraselenafulvalene --- radical-cation salts --- crystal and molecular structure --- electric conductivity --- n/a --- 1,1'-bis(o-carborane)
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This Special Issue on carboranes is dedicated to Prof. Alan Welch on the occasion of his retirement and his outstanding contributions to the field of carborane chemistry. Polyhedral carboranes lie at the interface of organic and inorganic chemistry. One of their most attractive and important features is the variety and beauty of their chemical structures. They have found applications as diverse as catalysis, in Boron Neutron Capture Therapy, as liquid crystals and as semiconductors. This Special Issue illustrates the very comprehensive world of heteroborane chemistry, from liquid crystals to BNCT agents, di-halogen bonding to quantum chemical calculations of tetrel complexes of the carbonium ylide CB11H11, nickellacarboranes as potential acid–base sensors to revealing how the selective formations of metallacarborane diastereomers can arise and metallacarboranes as function as radical cation salts with dielectric or semiconductor properties.
carboranes --- DFT --- reaction pathways --- boron chemistry --- o-carborane --- sulfa-Michael addition reaction --- cysteine --- boron neutron capture therapy --- o-carborane decapitation --- labeled compound --- 1,1′-bis(o-carborane) --- deboronation --- metalation --- bis(nickelation) --- diastereoisomers --- stereospecific --- boron clusters --- liquid crystals --- fluorescence --- cholesterol --- nido-carborane --- nitrilium derivatives --- nickel(II) half-sandwich complexes --- synthesis --- structure --- Lewis acid --- carborane --- carbonium ylide --- tetrel bond --- quantum chemistry --- electron density --- ELF --- iodo derivatives --- dihalogen bond --- X-ray structure --- quantum chemical calculations --- iron bis(1,2-dicarbollide) --- chromium bis(1,2-dicarbollide) --- tetramethyltetrathiafulvalene --- tetramethyltetraselenafulvalene --- radical-cation salts --- crystal and molecular structure --- electric conductivity --- n/a --- 1,1'-bis(o-carborane)
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