Banert, K. et al.: 2015 Science of Synthesis, 2014/4: Knowledge Updates 2014/4 DOI: 10.1055/sos-SD-101-00499
Knowledge Updates 2014/4

5.2.17.9 Acylstannanes (Including S, Se, and Te Analogues) (Update 2014)

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Book

Editors: Banert, K.; Hall, D. G.; Joule, J. A.; Moloney, M. G.; Reissig, H.-U.; Schaumann, E.

Authors: Bredenkamp, A.; Heimgartner, H.; Kantlehner, W.; Kirsch, S. F.; Kwiecień, H.; Lacôte, E.; Mlostoń, G.; Vallet, A.-L.; Wyatt, P. B.

Title: Knowledge Updates 2014/4

Print ISBN: 9783131763211; Online ISBN: 9783131975614; Book DOI: 10.1055/b-003-125861

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: Carreira, E. M.; Decicco, C. P.; Fürstner, A.; Molander, G. A.; Schaumann, E.; Shibasaki, M.; Thomas, E. J.; Trost, B. M.

Type: Multivolume Edition

 


Abstract

This chapter is an update to the earlier Science of Synthesis contribution (Section 5.2.17) describing synthetic methods that involve acylstannanes and analogues incorporating heavier chalcogens. This update focuses on applications of acylstannanes reported in the period 2000–2013. These include cross-coupling reactions with carbon electrophiles and transition-metal-catalyzed additions to carbon-carbon multiple bonds.

 
  • 5 Shirakawa E, Yamamoto Y, Nakao Y, Tsuchimoto T, Hiyama T. Chem. Commun. (Cambridge) 2001; 1926