The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
Abstract
A facile access to optically active 2-indolyl-1-nitro derivatives, which can be easily transformed into highly valuable compounds such as tryptamines and 1,2,3,4-tetrahydro-β-carbolines, is provided by the first catalytic enantioselective Friedel–Crafts alkylation of indoles with nitroalkenes (see scheme; e.g. R1=R2=H, R3=Ph).
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Cites
The Nitro Group in Organic Synthesis
Ono, N. (2001) · Wiley eBooks · doi:10.1002/0471224480 · Cited by 1,616
Okino, T., Hoashi, Y., & Takemoto, Y. (2003) · Journal of the American Chemical Society · doi:10.1021/ja036972z · Cited by 1,430
Metal-free organocatalysis through explicit hydrogen bonding interactions
Schreiner, P. R. (2003) · Chemical Society Reviews · doi:10.1039/b107298f · Cited by 1,276
Okino, T., Hoashi, Y., Furukawa, T., Xu, X., & Takemoto, Y. (2005) · Journal of the American Chemical Society · doi:10.1021/ja044370p · Cited by 1,061
Sigman, M. S., & Jacobsen, E. N. (1998) · Journal of the American Chemical Society · doi:10.1021/ja980139y · Cited by 910
New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction
Bandini, M., Melloni, A., & Umani‐Ronchi, A. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200301679 · Cited by 702
Hydrogen bond-directed cocrystallization and molecular recognition properties of diarylureas
Etter, M. C., Urbanczyk-Lipkowska, Z., Zia-Ebrahimi, M., & Panunto, T. W. (1990) · Journal of the American Chemical Society · doi:10.1021/ja00179a028 · Cited by 507
H-Bonding Additives Act Like Lewis Acid Catalysts
Schreiner, P. R., & Wittkopp, A. (2002) · Organic Letters · doi:10.1021/ol017117s · Cited by 475
Wittkopp, A., & Schreiner, P. R. (2003) · Chemistry – A European Journal · doi:10.1002/chem.200390042 · Cited by 414
Enantioselective Aza-Henry Reaction Catalyzed by a Bifunctional Organocatalyst
Okino, T., Nakamura, S., Furukawa, T., & Takemoto, Y. (2004) · Organic Letters · doi:10.1021/ol0364531 · Cited by 380
Cited by
Asymmetric Catalysis by Chiral Hydrogen‐Bond Donors
Taylor, M. S., & Jacobsen, E. N. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200503132 · Cited by 1,906
Augmenting large language models with chemistry tools
M. Bran, A., Cox, S., Schilter, O., Baldassari, C., White, A. D., & Schwaller, P. (2024) · Nature Machine Intelligence · doi:10.1038/s42256-024-00832-8 · Cited by 794
Metadata
- Authors
- Herrera, R. P., Sgarzani, V., Bernardi, L., & Ricci, A.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2005-10-07
- Volume
- 44
- Issue
- 40
- Pages
- 6576-6579
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W1964666522
- Cited by
- 465
- References
- 16
- FWCI
- 19.65
- Type
- journal article
- Language
- en
- Open access
- closed
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- Herrera, R. P., Sgarzani, V., Bernardi, L., & Ricci, A. (2005). Catalytic Enantioselective Friedel–Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200500227
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