Nucleophilic ring opening of trans -2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity
Abstract
We report the nucleophilic ring opening of unsymmetrical trans -epoxides to β-amino alcohols with catalyst-controlled regioselectivity.
- Authors:
-
- Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, USA
- Publication Date:
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1480555
- Grant/Contract Number:
- FG02-05ER15687
- Resource Type:
- Journal Article: Publisher's Accepted Manuscript
- Journal Name:
- ChemComm
- Additional Journal Information:
- Journal Name: ChemComm Journal Volume: 54 Journal Issue: 92; Journal ID: ISSN 1359-7345
- Publisher:
- Royal Society of Chemistry (RSC)
- Country of Publication:
- United Kingdom
- Language:
- English
Citation Formats
Lee, Michelle, Lamb, Jessica R., Sanford, Maria J., LaPointe, Anne M., and Coates, Geoffrey W. Nucleophilic ring opening of trans -2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity. United Kingdom: N. p., 2018.
Web. doi:10.1039/C8CC07200K.
Lee, Michelle, Lamb, Jessica R., Sanford, Maria J., LaPointe, Anne M., & Coates, Geoffrey W. Nucleophilic ring opening of trans -2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity. United Kingdom. https://doi.org/10.1039/C8CC07200K
Lee, Michelle, Lamb, Jessica R., Sanford, Maria J., LaPointe, Anne M., and Coates, Geoffrey W. 2018.
"Nucleophilic ring opening of trans -2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity". United Kingdom. https://doi.org/10.1039/C8CC07200K.
@article{osti_1480555,
title = {Nucleophilic ring opening of trans -2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity},
author = {Lee, Michelle and Lamb, Jessica R. and Sanford, Maria J. and LaPointe, Anne M. and Coates, Geoffrey W.},
abstractNote = {We report the nucleophilic ring opening of unsymmetrical trans -epoxides to β-amino alcohols with catalyst-controlled regioselectivity.},
doi = {10.1039/C8CC07200K},
url = {https://www.osti.gov/biblio/1480555},
journal = {ChemComm},
issn = {1359-7345},
number = 92,
volume = 54,
place = {United Kingdom},
year = {Thu Nov 15 00:00:00 EST 2018},
month = {Thu Nov 15 00:00:00 EST 2018}
}
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Cited by: 23 works
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