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Jiang, X. et al.: 2021 Science of Synthesis, 2021/1: Knowledge Updates 2021/1 DOI: 10.1055/sos-SD-132-00285
Knowledge Updates 2021/1

32.3.7.2 1-(Organochalcogeno)-2-(organooxy)alkenes (Update 2021)

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Book

Editors: Jiang, X.; Marek, I.; Marschner, C.; Montchamp, J.-L.; Reissig, H.-U.; Wang, M.

Authors: Błażewska, K.; Feng, X. M.; Grimmer, J.; Gudat, D. ; Hlina, J. A. ; Justyna, K.; Kashemirov, B. A.; Krieg, S.-C.; Li, W.; Liu, X. H.; Lyu, J.; Manolikakes, G. ; McKenna, C. E.; Singh, F. V. 

Title: Knowledge Updates 2021/1

Print ISBN: 9783132441958; Online ISBN: 9783132441972; Book DOI: 10.1055/b000000476

1st edition © 2021 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

Science of Synthesis Knowledge Updates



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: 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.

Type: Multivolume Edition

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Abstract

This is an update to the earlier Science of Synthesis contribution (Section 32.3.7) covering the synthesis and use of 1-(organochalcogeno)-2-(organooxy)alkenes. It focuses on the literature published in the period 2006 to 2019.

Key words

alkenes - sulfur compounds - microwaves - radical vinylation - rearrangements - multicomponent reactions - ring-closing metathesis - dehydrogenation
 
  • 1 Tejedor D, Méndez-Abt G, García-Tellado F. Chem.–Eur. J. 2010; 16: 428
    PubMed
  • 2 Delgado E, Hernández E, Nievas Á, Martín A, Recio MJ. J. Organomet. Chem. 2010; 695: 446
  • 3 Villuendas P, Ruiz S, Vidossich P, Lledós A, Urriolabeitia EP. Chem.–Eur. J. 2018; 24: 13 124
  • 4 Evans PA, Manangan T. J. Org. Chem. 2000; 65: 4523
    PubMed
  • 5 Chéry F, Desroses M, Tatibouët A, De Lucchi O, Rollin P. Tetrahedron 2003; 59: 4563
  • 6 Berlin S, Ericsson C, Engman L. J. Org. Chem. 2003; 68: 8386
    PubMed
  • 7 Kimura T, Nakata T. Tetrahedron: Asymmetry 2010; 21: 1389
  • 8 Yan Z, Kahn M, Qabar M, Urban J, Kim H.-O, Blaskovich MA. Bioorg. Med. Chem. Lett. 2003; 13: 2083
  • 9 Waters MS, Onofiok E, Tellers DM, Chilenski JR, Song ZJ. Synthesis 2006; 3389
  • 10 Morgans GL, Ngidi EL, Madeley LG, Khanye SD, Michael JP, de Koning CB, van Otterlo WAL. Tetrahedron 2009; 65: 10 650
  • 11 Wang T, Gao Z.-H, Ye S. Adv. Synth. Catal. 2017; 359: 3479
  • 12 Montermini F, Lacôte E, Malacria M. Org. Lett. 2004; 6: 921
    PubMed
  • 13 Chéry F, Cabianca E, Tatibouët A, De Lucchi O, Rollin P. Tetrahedron 2012; 68: 544
  • 14 Sugimura H, Kusakabe K. Synlett 2013; 24: 69
  • 15 Chavan SP, Chittiboyina AG, Ramakrishna G, Tejwani RB, Ravindranathan T, Kamat SK, Rai B, Sivadasan L, Balakrishnan K, Ramalingam S, Deshpande VH. Tetrahedron 2005; 61: 9273
  • 16 Klose I, Misale A, Maulide N. J. Org. Chem. 2016; 81: 7201
    PubMed
  • 17 Virolleaud M.-A, Sridharan V, Mailhol D, Bonne D, Bressy C, Chouraqui G, Commeiras L, Coquerel Y, Rodriguez J. Tetrahedron 2009; 65: 9756
  • 18 Rasool N, Rashid MA, Reinke H, Fischer C, Langer P. Tetrahedron 2007; 63: 11 626
  • 19 Heredia AA, Soria-Castro SM, Bouchet LM, Oksdath-Mansilla G, Barrionuevo CA, Caminos DA, Bisogno FR, Argüello JE, Peñéñory AB. Org. Biomol. Chem. 2014; 12: 6516
    PubMed
  • 20 Kitagaki S, Kawamura T, Shibata D, Mukai C. Tetrahedron 2008; 64: 11 086
  • 21 Hsueh N.-C, Hsiao Y.-T, Chang M.-Y. Tetrahedron 2017; 73: 4398
  • 22 Yu H, Han J, Chen J, Deng H, Shao M, Zhang H, Cao W. Eur. J. Org. Chem. 2012; 3142