Suzuki cross-coupling on enantiomerically pure epoxides: efficient synthesis of diverse, modular amino alcohols from single enantiopure precursors.

Cattoën X, Pericàs MA

DOI: 10.1021/jo062612t
Published: 2007 Apr 27
Container: The Journal of organic chemistry
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1021/jo062612t,
  title = {Suzuki cross-coupling on enantiomerically pure epoxides: efficient synthesis of diverse, modular amino alcohols from single enantiopure precursors.},
  author = {Cattoën X and Pericàs MA},
  year = {2007},
  journal = {The Journal of organic chemistry},
  doi = {10.1021/jo062612t},
  url = {https://doi.org/10.1021/jo062612t}
}

RIS

TY  - JOUR
TI  - Suzuki cross-coupling on enantiomerically pure epoxides: efficient synthesis of diverse, modular amino alcohols from single enantiopure precursors.
AU  - Cattoën X
AU  - Pericàs MA
PY  - 2007
JO  - The Journal of organic chemistry
DO  - 10.1021/jo062612t
UR  - https://doi.org/10.1021/jo062612t
ER  -

APA

X, C., & MA, P. (2007). Suzuki cross-coupling on enantiomerically pure epoxides: efficient synthesis of diverse, modular amino alcohols from single enantiopure precursors.. The Journal of organic chemistry. https://doi.org/10.1021/jo062612t

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pubmed · retrieved 2026-09-25T05:43:06.750Z