Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines
- DOI
- 10.1021/jo202580y
- Published
- 2012-02-29
- Container
- The Journal of Organic Chemistry
- Publisher
- American Chemical Society (ACS)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/jo202580y,
title = {Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines},
author = {Damien Campolo and Anouk Gaudel-Siri and Shovan Mondal and Didier Siri and Eric Besson and Nicolas Vanthuyne and Malek Nechab and Michèle P. Bertrand},
year = {2012},
journal = {The Journal of Organic Chemistry},
doi = {10.1021/jo202580y},
url = {https://doi.org/10.1021/jo202580y}
}RIS
TY - JOUR TI - Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines AU - Damien Campolo AU - Anouk Gaudel-Siri AU - Shovan Mondal AU - Didier Siri AU - Eric Besson AU - Nicolas Vanthuyne AU - Malek Nechab AU - Michèle P. Bertrand PY - 2012 JO - The Journal of Organic Chemistry DO - 10.1021/jo202580y UR - https://doi.org/10.1021/jo202580y ER -
APA
Campolo, D., Gaudel-Siri, A., Mondal, S., Siri, D., Besson, E., Vanthuyne, N., Nechab, M., & Bertrand, M. P. (2012). Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines. The Journal of Organic Chemistry. https://doi.org/10.1021/jo202580y
Source records
- crossref · retrieved 2026-09-25T06:20:46.406Z