Enantiospecific sp2–sp3 coupling of secondary and tertiary boronic esters-Reference-Cited by-同舟云学术

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Enantiospecific sp2–sp3 coupling of secondary and tertiary boronic esters

Published:2014-06-08 Issue:7 Volume:6 Page:584-589
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nature Chem

Author:

Bonet Amadeu,Odachowski Marcin,Leonori Daniele,Essafi Stephanie,Aggarwal Varinder K.

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

http://www.nature.com/articles/nchem.1971.pdf

Reference50 articles.

1. Suzuki, A. Cross-coupling reactions of organoboranes: an easy way to construct C–C bonds (Nobel Lecture). Angew. Chem. Int. Ed. 50, 6722–6737 (2011).

2. Miyaura, N. & Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 95, 2457–2483 (1995).

3. Molander, G. A. & Wisniewski, S. R. Stereospecific cross-coupling of secondary organotrifluoroborates: potassium 1-(benzyloxy)alkyltrifluoroborates. J. Am. Chem. Soc. 134, 16856–16868 (2012).

4. Awano, T., Ohmura, T. & Suginome, M. Inversion or retention? Effects of acidic additives on the stereochemical course in enantiospecific Suzuki–Miyaura coupling of α-(acetylamino)benzylboronic esters. J. Am. Chem. Soc. 133, 20738–20741 (2011).

5. Ohmura, T., Awano, T. & Suginome, M. Stereospecific Suzuki−Miyaura coupling of chiral α-(acylamino)benzylboronic esters with inversion of configuration. J. Am. Chem. Soc. 132, 13191–13193 (2010).

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