Anionic Annulations in Organic Synthesis

- A Versatile and Prolific Class of Ring-Forming Reactions

  • Format
  • Bog, paperback
  • Engelsk

Beskrivelse

Anionic Annulations in Organic Synthesis: A Versatile and Prolific Class of Ring-Forming Reactions is a comprehensive review of the main annulations for the construction of cyclic structures and their use in the total synthesis of functional molecules. The book explores in detail the Hauser, Robinson, Sammes, and Myers annulations, all of which are beneficial to constructing substrates with complex molecular structures suitable for pharmaceutical purposes. This volume begins with an in-depth introduction on the history and perspectives of annulations. It then covers different categories of annulation in each chapter, examining their application to drug synthesis for a range of different medicinal compounds. Anionic Annulations in Organic Synthesis delivers a thorough analysis of the topic and provides the tools necessary to master anionic organic chemistry. It is a valuable resource for chemists, researchers, and students seeking a complete and detailed understanding of anionic annulations.

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  • Vægt750 g
  • coffee cup img
    10 cm
    book img
    15,2 cm
    22,9 cm

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    History Synthesis Anthraquinones Definitions Donors Importance Classifications Total Synthesis Setbacks Anthracyclines 4-Naphthoquinones 4-Quinones Annulations Angucyclines Aryne annulation annulation Aquayamycin Benzylic Anionic Aromatic polyketides Arynes Averufin C3-nucleofugal phthalides Apex reaction Chlorocyclinone A Chen annulation Chi annulation Dötz annulation Cycloalkenone acceptors Competing reactions Clausevatine D Euplectin Condensed aromatics and heterocyclics Coriandrin synthesis Hauser-Leusen annulation Danheiser Annulation Hibarimicinone Deslongchamps [4 + 2] annulation Hauser annulation Homophthalic anhydrides β-Methoxy unsaturated ester and ketone acceptors α-Naphthols Landomycin A Leusen annulation Larock annulation Friedlӓnder annulation Linearly fused polycyclic aromatics Fredericamycin A N-Heterocyclic carbenes Nonactivated phthalides Myers annulation Nair annulation Naphthols Phthalides o-Toluates Imines and nitroethenes acceptors γ-Citromycinone Phthalide cyanide Phthalides without a C3-nucleofuge Sammes annulation Selective tranformations reaction conditions Lateral lithiation Sulfoxide/sulfone activated o-toluate/o-tolualdehyde donors Lupton annulation Padwa annulation Staunton-Weinreb annulation Tamura [4 + 2] annulation Transannulation Tri-O-methylolivin Uncialamycin Wadsworth-Emmons cyclopropanation Mal annulation Nonactivated o-toluate donors Thiophthalides Phthalide sulfone Naphthoquinones McCoy cyclopropanation Polyaromatic phenols Trioxacarcin A Tetracyclines and carbazoles Viridicatumtoxin B

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