Synthesis of 6-deoxy-homoDMDP and its C(5)-epimer: absolute stereochemistry of natural products from Hyacinthus orientalis

Jean-Bernard Behr, Georges Guillerm

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DOI: 10.1016/s0957-4166(02)00081-2
Published: 2002-02
Container: Tetrahedron: Asymmetry
Publisher: Elsevier BV
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1016/s0957-4166-02-00081-2,
  title = {Synthesis of 6-deoxy-homoDMDP and its C(5)-epimer: absolute stereochemistry of natural products from Hyacinthus orientalis},
  author = {Jean-Bernard Behr and Georges Guillerm},
  year = {2002},
  journal = {Tetrahedron: Asymmetry},
  doi = {10.1016/s0957-4166(02)00081-2},
  url = {https://doi.org/10.1016/s0957-4166(02)00081-2}
}

RIS

TY  - JOUR
TI  - Synthesis of 6-deoxy-homoDMDP and its C(5)-epimer: absolute stereochemistry of natural products from Hyacinthus orientalis
AU  - Jean-Bernard Behr
AU  - Georges Guillerm
PY  - 2002
JO  - Tetrahedron: Asymmetry
DO  - 10.1016/s0957-4166(02)00081-2
UR  - https://doi.org/10.1016/s0957-4166(02)00081-2
ER  -

APA

Behr, J., & Guillerm, G. (2002). Synthesis of 6-deoxy-homoDMDP and its C(5)-epimer: absolute stereochemistry of natural products from Hyacinthus orientalis. Tetrahedron: Asymmetry. https://doi.org/10.1016/s0957-4166(02)00081-2

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crossref · retrieved 2026-09-26T13:32:21.656Z