Nucleophilic ring opening of trans -2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity

Lee, Michelle; Lamb, Jessica R.; Sanford, Maria J.; LaPointe, Anne M.; Coates, Geoffrey W.

doi:10.1039/C8CC07200K

Title: Nucleophilic ring opening of trans -2,3-disubstituted epoxides to β-amino alcohols with catalyst-controlled regioselectivity

Journal Article · Thu Nov 15 00:00:00 EST 2018 · ChemComm

DOI:https://doi.org/10.1039/C8CC07200K· OSTI ID:1480555

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Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, USA

We report the nucleophilic ring opening of unsymmetrical trans -epoxides to β-amino alcohols with catalyst-controlled regioselectivity.

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Sponsoring Organization:: USDOE

Grant/Contract Number:: FG02-05ER15687

OSTI ID:: 1480555

Journal Information:: ChemComm, Journal Name: ChemComm Vol. 54 Journal Issue: 92; ISSN 1359-7345

Publisher:: Royal Society of Chemistry (RSC)Copyright Statement

Country of Publication:: United Kingdom

Language:: English

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Cited by: 23 works

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