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Donohoe, T. J. et al.: 2022 Science of Synthesis, 2022/3: Knowledge Updates 2022/3 DOI: 10.1055/sos-SD-148-00042
Knowledge Updates 2022/3

48.2.3 Cyclopropanes (Update 2022)

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Buch

Herausgeber: Donohoe, T. J.; Huang, Z. ; Marschner, C. ; Oestreich, M. 

Autoren: Jackowski, O. ; Marschner, C. ; Ohmiya, H. ; Perez-Luna, A. ; Pinto, D. C. G. A. ; Rocha, D. H. A. ; dos Santos, C. M. M. ; Silva, V. L. M. ; Sumida, Y. ; Takeda, N. ; Tang, X.; Yoshida, H. 

Titel: Knowledge Updates 2022/3

Print ISBN: 9783132452848; Online ISBN: 9783132452862; Buch-DOI: 10.1055/b000000643

1st edition © 2022 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart

Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie

Science of Synthesis Knowledge Updates



Übergeordnete Publikation

Titel: Science of Synthesis

DOI: 10.1055/b-00000101

Reihenherausgeber: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.

Typ: Mehrbändiges Werk

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Abstract

Cyclopropanes represent an interesting class of strained rings and serve as versatile building blocks in organic synthesis. Furthermore, cyclopropane moieties are also found in many bioactive compounds and natural products. Reviewed herein are synthetic strategies to access mono- and polysubstituted cyclopropyl cores. In particular, the application of visible-light photoredox catalysis in the synthesis of cyclopropanes is introduced.

Schlüsselwörter

cyclopropanes - cycloaddition - 1,3-elimination - decarbonylation - photoredox catalysis - carbenes - cycloisomerization - ring contraction
 
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