Supporting Information
| Supporting Information File 1: Detailed experimental procedures of chiral ligands L2, L5, and L6. | ||
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Cite the Following Article
Rational design of cyclopropane-based chiral PHOX ligands for intermolecular asymmetric Heck reaction
Marina Rubina, William M. Sherrill, Alexey Yu. Barkov and Michael Rubin
Beilstein J. Org. Chem. 2014, 10, 1536–1548.
https://doi.org/10.3762/bjoc.10.158
How to Cite
Rubina, M.; Sherrill, W. M.; Barkov, A. Y.; Rubin, M. Beilstein J. Org. Chem. 2014, 10, 1536–1548. doi:10.3762/bjoc.10.158
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- Xie, J.; Liang, R.-X.; Jia, Y. Recent Advances of Catalytic Enantioselective Heck Reactions and Reductive-Heck Reactions. Chinese Journal of Chemistry 2021, 39, 710–728. doi:10.1002/cjoc.202000464
- Shintani, R.; Ohzono, A.; Shirota, K. Phosphinative cyclopropanation of allyl phosphates with lithium phosphides. Chemical communications (Cambridge, England) 2020, 56, 11851–11854. doi:10.1039/d0cc04854b
- Larock, R. C.; Zeni, G. Comprehensive Organic Transformations; Wiley, 2018; pp 1–49. doi:10.1002/9781118662083.cot02-001
- Edwards, A. J.; Rubina, M.; Rubin, M. Directed RhI‐Catalyzed Asymmetric Hydroboration of Prochiral 1‐Arylcycloprop‐2‐Ene‐1‐Carboxylic Acid Derivatives. Chemistry (Weinheim an der Bergstrasse, Germany) 2017, 24, 1394–1403. doi:10.1002/chem.201704443
- Song, C.; Dang, Y.; Tao, Y.; Wang, Z.-X. DFT Mechanistic Study of Functionalizations of ω-Ene-Cyclopropanes and Alkylidenecyclopropanes via Allylic C–H and C–C Bond Cleavage Facilitated by a Zirconocene Complex. Organometallics 2015, 34, 5233–5244. doi:10.1021/acs.organomet.5b00650
- Edwards, A. J.; Ryabchuk, P.; Barkov, A. Y.; Rubina, M.; Rubin, M. Preparative resolution of bromocyclopropylcarboxylic acids. Tetrahedron: Asymmetry 2014, 25, 1537–1549. doi:10.1016/j.tetasy.2014.10.017
- Lauer, M. G.; Thompson, M. K.; Shaughnessy, K. H. Controlling olefin isomerization in the heck reaction with neopentyl phosphine ligands. The Journal of organic chemistry 2014, 79, 10837–10848. doi:10.1021/jo501840u
