The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
Catalytic asymmetric allylic alkylation employing heteroatom nucleophiles: a powerful method for C–X bond formation
Abstract
Metal catalyzed asymmetric allylic alkylation (AAA) reactions have been an extensively studied and fruitful area of research in organic chemistry. The use of heteroatom-centered nucleophiles in this reaction is a powerful method for asymmetric C–X (X = heteroatom) bond formation. This perspective summarizes developments and applications of metal catalyzed AAA reactions employing heteroatom nucleophiles.
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Cites
The Atom Economy—A Search for Synthetic Efficiency
Trost, B. (1991) · Science · doi:10.1126/science.1962206 · Cited by 4,798
Self-citationAsymmetric Transition Metal-Catalyzed Allylic Alkylations
Trost, B. M., & Vranken, D. L. V. (1996) · Chemical Reviews · doi:10.1021/cr9409804 · Cited by 3,205
Self-citationAsymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
Trost, B. M., & Crawley, M. L. (2003) · Chemical Reviews · doi:10.1021/cr020027w · Cited by 2,845
Self-citationShaikh, A.-A. G., & Sivaram, S. (1996) · Chemical Reviews · doi:10.1021/cr950067i · Cited by 1,381
von Matt, P., & Pfaltz, A. (1993) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199305661 · Cited by 665
Trost, B. M., Machacek, M. R., & Aponick, A. (2006) · Accounts of Chemical Research · doi:10.1021/ar040063c · Cited by 535
Self-citationTogni, A., Burckhardt, U., Gramlich, V., Pregosin, P. S., & Salzmann, R. (1996) · Journal of the American Chemical Society · doi:10.1021/ja953031g · Cited by 288
Total Syntheses of Furaquinocin A, B, and E
Trost, B. M., Thiel, O. R., & Tsui, H. (2003) · Journal of the American Chemical Society · doi:10.1021/ja0364118 · Cited by 158
Self-citationTrost, B. M., & Oslob, J. D. (1999) · Journal of the American Chemical Society · doi:10.1021/ja983617d · Cited by 110
Self-citationNelson, S. G., Bungard, C. J., & Wang, K. (2003) · Journal of the American Chemical Society · doi:10.1021/ja037655v · Cited by 106
Cited by
Catalytic Transformations of Functionalized Cyclic Organic Carbonates
Guo, W., Gómez, J. E., Cristòfol, À., Xie, J., & Kleij, A. W. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201805009 · Cited by 371
All-carbon quaternary centers in natural products and medicinal chemistry: recent advances
Ling, T., & Rivas, F. (2016) · Tetrahedron · doi:10.1016/j.tet.2016.09.002 · Cited by 312
Metadata
- Authors
- Trost, B. M., Zhang, T., & Sieber, J. D.
- Venue
- Chemical Science
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2010
- Volume
- 1
- Issue
- 4
- Pages
- 427
- ISSN
- 2041-6520 (ISSN-L)
- 2041-6539
- OpenAlex
- W2156818195
- Cited by
- 386
- References
- 15
- FWCI
- 15.94
- Type
- journal article
- Language
- en
- Open access
- closed
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- Trost, B. M., Zhang, T., & Sieber, J. D. (2010). Catalytic asymmetric allylic alkylation employing heteroatom nucleophiles: a powerful method for C–X bond formation. Chemical Science. https://doi.org/10.1039/c0sc00234h
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