A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using a hetero Diels–Alder/allylboration sequence
- DOI
- 10.1039/b208572k
- Published
- 2002-12-20
- Container
- Chemical Communications
- Publisher
- Royal Society of Chemistry (RSC)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1039/b208572k,
title = {A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using a hetero Diels–Alder/allylboration sequence},
author = {Michael Deligny and François Carreaux and Bertrand Carboni and Loïc Toupet and Gilles Dujardin},
year = {2002},
journal = {Chemical Communications},
doi = {10.1039/b208572k},
url = {https://doi.org/10.1039/b208572k}
}RIS
TY - JOUR TI - A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using a hetero Diels–Alder/allylboration sequence AU - Michael Deligny AU - François Carreaux AU - Bertrand Carboni AU - Loïc Toupet AU - Gilles Dujardin PY - 2002 JO - Chemical Communications DO - 10.1039/b208572k UR - https://doi.org/10.1039/b208572k ER -
APA
Deligny, M., Carreaux, F., Carboni, B., Toupet, L., & Dujardin, G. (2002). A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using a hetero Diels–Alder/allylboration sequence. Chemical Communications. https://doi.org/10.1039/b208572k
Source records
- crossref · retrieved 2026-11-10T08:00:49.939Z