A novel diastereoselective route to α-hydroxyalkyl dihydropyrans using a hetero Diels–Alder/allylboration sequence

Michael Deligny, François Carreaux, Bertrand Carboni, Loïc Toupet, Gilles Dujardin

Open source

DOI
10.1039/b208572k
Published
2002-12-20
Container
Chemical Communications
Publisher
Royal Society of Chemistry (RSC)
Open access
unknown

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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

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