An Expeditious Route to Both Enantiomers of All Carbon Quaternary Stereocenters at C-3 Carbon of Lactams via [3,3]-Sigmatropic Rearrangement: Total Synthesis of (−)-Physostigmine
- DOI
- 10.1021/ol503766y
- Published
- 2015-02-11
- Container
- Organic Letters
- Publisher
- American Chemical Society (ACS)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/ol503766y,
title = {An Expeditious Route to Both Enantiomers of All Carbon Quaternary Stereocenters at C-3 Carbon of Lactams via [3,3]-Sigmatropic Rearrangement: Total Synthesis of (−)-Physostigmine},
author = {Ganesh Pandey and Jagadish Khamrai and Akash Mishra},
year = {2015},
journal = {Organic Letters},
doi = {10.1021/ol503766y},
url = {https://doi.org/10.1021/ol503766y}
}RIS
TY - JOUR TI - An Expeditious Route to Both Enantiomers of All Carbon Quaternary Stereocenters at C-3 Carbon of Lactams via [3,3]-Sigmatropic Rearrangement: Total Synthesis of (−)-Physostigmine AU - Ganesh Pandey AU - Jagadish Khamrai AU - Akash Mishra PY - 2015 JO - Organic Letters DO - 10.1021/ol503766y UR - https://doi.org/10.1021/ol503766y ER -
APA
Pandey, G., Khamrai, J., & Mishra, A. (2015). An Expeditious Route to Both Enantiomers of All Carbon Quaternary Stereocenters at C-3 Carbon of Lactams via [3,3]-Sigmatropic Rearrangement: Total Synthesis of (−)-Physostigmine. Organic Letters. https://doi.org/10.1021/ol503766y
Source records
- crossref · retrieved 2026-09-25T07:03:27.762Z