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I. Namboothiri - One of the best experts on this subject based on the ideXlab platform.
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BAER–FISCHER Amino Sugar Synthesis to BURTON Aromatic Trifluoromethylation
Organic Syntheses Based on Name Reactions, 2012Co-Authors: Alfred Hassner, I. NamboothiriAbstract:This article contains brief overviews, mechanisms and practical details for organic synthesis named reactions and processes beginning with the letter ‘B’. Reactions included in this section are: BAER–FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER–DREWSON Indoxyl Synthesis; BAEYER Oxindole Synthesis; BAEYER–VILLIGER Aromatic Tritylation; BAEYER–VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER–VENKATARAMAN Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY–SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD–STEVENS Tosylhydrazone Decomposition; BARBAS–LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER–WIELAND Ester Chain Degradation; BARDHAN–SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination Reagent; BARTON Arylation; BARTON Deamination; BARTON Decarboxylation; BARTON Nitrite Photolysis; BARTON–KELLOG Olefination; BARTON–McCOMBIE Alcohol Deoxygenation; BART–SCHELLER Aromatic Arsonylation; BAUDISCH Nitrosophenol Synthesis; BECHAMP Phenol, Aniline Arsonilation; BECKMANN Oxime Rearrangement or Fragmentation; BELLER Multicomponent Amino Acid Synthesis; BENARY Conjugated Aldehyde Synthesis; BERCHTOLD Enamine Homologation; BERGMAN Cycloaromatization; BERNTHSEN Acridine Synthesis; BERTRAND–STEPHAN Metal-free Bond Activation; BESTMANN Cumulene Ylides; BIGINELLI Pyrimidone Synthesis; BIRCH Na-NH 3 Reduction; BISCHLER Benzotriazine Synthesis; BISCHLER–MOHLAU Indole Synthesis; BISCHLER–NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC–QUELLET Chloroalkylation; BLICKE–PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX–CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels–Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE – BEECH Aromatic Aldehyde Synthesis; BOULTON–KATRITZKY Heterocyclic Rearrangement; BOUVEAULT Aldehyde Synthesis; BOUVEAULT–LOCQUIN Amino Acid Synthesis; BOUVEAULT–BLANC Ester Reduction; BOYLAND–SIMS o-Hydroxyaniline Synthesis; BRADSHER Isoquinolinium Cycloaddition; BRADSHER Aromatic Cyclization; BRANDI – GUARNA Spirocyclopropane Rearrangement; BRECKPORT β -Lactam Synthesis; BREDERECK Imidazole Synthesis; Brook Silaketone Rearrangement; von BRAUN Amine Degradation; BROWN Acetylene Zipper Reaction; BROWN Anti Aldol via B -enolate; BROWN Asymmetric Allylation; BROWN Functional Groups via Hydroboration; BROWN Ketone Synthesis by Hydroboration; BROWN Stereoselective Reducing Agents; BROWN Asymmetric Ketone Reduction; BRUYLANT S Aldehyde Aminoalkylation; BUCHERER–BERGS Hydantoin Synthesis; BUCHERER–LE PETIT Naphthol (Naphthylamine) Synthesis; BUCHNER–CURTIUS C O Homologation; BUCHWALD Heterocyclization; BUCHWALD – HARTWIG Aryl Halide Amination; BURGESS Alcohol Dehydrating Reagent; BURTON Aromatic Trifluoromethylation
Alfred Hassner - One of the best experts on this subject based on the ideXlab platform.
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BAER–FISCHER Amino Sugar Synthesis to BURTON Aromatic Trifluoromethylation
Organic Syntheses Based on Name Reactions, 2012Co-Authors: Alfred Hassner, I. NamboothiriAbstract:This article contains brief overviews, mechanisms and practical details for organic synthesis named reactions and processes beginning with the letter ‘B’. Reactions included in this section are: BAER–FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER–DREWSON Indoxyl Synthesis; BAEYER Oxindole Synthesis; BAEYER–VILLIGER Aromatic Tritylation; BAEYER–VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER–VENKATARAMAN Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY–SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD–STEVENS Tosylhydrazone Decomposition; BARBAS–LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER–WIELAND Ester Chain Degradation; BARDHAN–SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination Reagent; BARTON Arylation; BARTON Deamination; BARTON Decarboxylation; BARTON Nitrite Photolysis; BARTON–KELLOG Olefination; BARTON–McCOMBIE Alcohol Deoxygenation; BART–SCHELLER Aromatic Arsonylation; BAUDISCH Nitrosophenol Synthesis; BECHAMP Phenol, Aniline Arsonilation; BECKMANN Oxime Rearrangement or Fragmentation; BELLER Multicomponent Amino Acid Synthesis; BENARY Conjugated Aldehyde Synthesis; BERCHTOLD Enamine Homologation; BERGMAN Cycloaromatization; BERNTHSEN Acridine Synthesis; BERTRAND–STEPHAN Metal-free Bond Activation; BESTMANN Cumulene Ylides; BIGINELLI Pyrimidone Synthesis; BIRCH Na-NH 3 Reduction; BISCHLER Benzotriazine Synthesis; BISCHLER–MOHLAU Indole Synthesis; BISCHLER–NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC–QUELLET Chloroalkylation; BLICKE–PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX–CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels–Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE – BEECH Aromatic Aldehyde Synthesis; BOULTON–KATRITZKY Heterocyclic Rearrangement; BOUVEAULT Aldehyde Synthesis; BOUVEAULT–LOCQUIN Amino Acid Synthesis; BOUVEAULT–BLANC Ester Reduction; BOYLAND–SIMS o-Hydroxyaniline Synthesis; BRADSHER Isoquinolinium Cycloaddition; BRADSHER Aromatic Cyclization; BRANDI – GUARNA Spirocyclopropane Rearrangement; BRECKPORT β -Lactam Synthesis; BREDERECK Imidazole Synthesis; Brook Silaketone Rearrangement; von BRAUN Amine Degradation; BROWN Acetylene Zipper Reaction; BROWN Anti Aldol via B -enolate; BROWN Asymmetric Allylation; BROWN Functional Groups via Hydroboration; BROWN Ketone Synthesis by Hydroboration; BROWN Stereoselective Reducing Agents; BROWN Asymmetric Ketone Reduction; BRUYLANT S Aldehyde Aminoalkylation; BUCHERER–BERGS Hydantoin Synthesis; BUCHERER–LE PETIT Naphthol (Naphthylamine) Synthesis; BUCHNER–CURTIUS C O Homologation; BUCHWALD Heterocyclization; BUCHWALD – HARTWIG Aryl Halide Amination; BURGESS Alcohol Dehydrating Reagent; BURTON Aromatic Trifluoromethylation
