Towards EPC-syntheses of the structural class of cochleamycins and macquarimicins. Part 1: EPC-synthesis of the hydrindene subunit of the cochleamycins

Dehydrogenation Dehydrohalogenation and Elimination of Alkyl Halides 1,1‐Dihalides 1,2‐Dihalides 1,3‐Dihalides Trihaloalkanes β‐Halo Ethers Halohydrins Halo Aldehydes and Ketones Halo Carboxylic Acids Halo Esters β‐Halo Sulfonates Amines β‐Halo Amines and Derivatives Amine Oxides (Cope Elimination) Quaternary Ammonium Salts N ‐Alkyl‐ N , N ‐Disulfonimides N ‐Nitrosocarboxamides Nitro Compounds Diazo Compounds β‐Substituted Azides Ethers β‐Substituted Ethers Sulfides α‐Halosulfides β‐Halosulfides β‐Hydroxysulfides Sulfoxides β‐Alkoxy‐ and Hydroxy‐Sulfoxides Sulfones α‐Halosulfones (Ramberg—Bäcklund Reaction) β‐Hydroxysulfones β‐Acyloxysulfones Other β‐Substituted Sulfones Disulfones Sulfonyl Halides β‐Oxyselenides Selenoxides Tellurides Organosilanes β‐Halosilanes β‐Oxysilanes and ‐Stannanes β‐Aminosilanes Dehydration of Alcohols Sulfonate Esters Sulfates Phosphates and Thiophosphates Xanthates Thiocarbonates Carbamates N ‐Methyl‐4‐alkoxypyridinium Iodides 1,2‐Diols and Derivatives 1,2‐Disulfonates 1,3‐Diols Acetals Dithioacetals Aldehydes and Ketones Lactols Carboxylic Acids Acid Halides Acid Anhydrides Esters and Lactones Amides and Lactams Nitriles Miscellaneous Reactions

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Formation of Alkenes by Diels–Alder Reactions

Larock

2018

Comprehensive Organic Transformations

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General Reviews Regioselectivity Exo / Endo Selectivity Asymmetric Diels–Alder Reaction Mechanism Use of High Pressure Microwave Irradiation Infrared Irradiation Mechanical Ball Milling Ultracentrifugation Use of Ultrasound Catalysis Solvent Effects Cavity Effects Retro‐Diels–Alder Reaction Intramolecular Diels–Alder Reaction Inverse Electron‐Demand Diels–Alder Reaction Radical Cation Diels–Alder Reaction Ionic Diels–Alder Reaction Use of Heterodienophiles Use of Heteroatom‐Containing “Dienes” Use of Substituted 1,3‐Dienes o ‐Quinodimethanes and Heterocyclic Analogues Arynes and Hetarynes Some Other Dienophiles Dienophile Equivalents Transition Metal Carbenes as Dienophiles

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Towards EPC-syntheses of the structural class of cochleamycins and macquarimicins. Part 1: EPC-synthesis of the hydrindene subunit of the cochleamycins

Cited by 6 publications

References 140 publications

2,4,6-Triisopropylbenzenesulfonylhydrazide

2,4,6-Triisopropylbenzenesulfonylhydrazide

Formation of Alkenes by Elimination

Formation of Alkenes by Diels–Alder Reactions

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