Stereoretentive Pd-catalysed Stille cross-coupling reactions of secondary alkyl azastannatranes and aryl halides
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemical Engineering,General Chemistry
Link
http://www.nature.com/articles/nchem.1652.pdf
Reference47 articles.
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2. Netherton, M. R. & Fu, G. C. in Topics in Organometallic Chemistry: Palladium in Organic Synthesis (ed. Tsuji, J.) 85–108 (Springer, 2005).
3. Rudolph, A. & Lautens, M. Secondary alkyl halides in transition metal-catalyzed cross-coupling reactions. Angew. Chem. Int. Ed. 48, 2656–2670 (2009).
4. Chemler, S. R., Trauner, D. & Danishefsky, S. J. The β-alkyl Suzuki–Miyaura cross-coupling reaction: development, mechanistic study, and applications in natural product synthesis. Angew. Chem. Int. Ed. 40, 4544–4568 (2001).
5. Luo, X. et al. Superior effect of a π-acceptor ligand (phosphine-electron-deficient olefin ligand) in the Negishi coupling involving alkylzinc reagents. Org. Lett. 9, 4571–4574 (2007).
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