Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II.
- DOI
- 10.1039/c2ob25622c
- Published
- 2012 Sep 14
- Container
- Organic & biomolecular chemistry
- Publisher
- Not recorded
- Open access
- unknown
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BibTeX
@article{allodium:10.1039/c2ob25622c,
title = {Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II.},
author = {Kumar P and Dubey A and Harbindu A},
year = {2012},
journal = {Organic \& biomolecular chemistry},
doi = {10.1039/c2ob25622c},
url = {https://doi.org/10.1039/c2ob25622c}
}RIS
TY - JOUR TI - Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II. AU - Kumar P AU - Dubey A AU - Harbindu A PY - 2012 JO - Organic & biomolecular chemistry DO - 10.1039/c2ob25622c UR - https://doi.org/10.1039/c2ob25622c ER -
APA
P, K., A, D., & A, H. (2012). Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II.. Organic & biomolecular chemistry. https://doi.org/10.1039/c2ob25622c
Source records
- pubmed · retrieved 2026-09-25T03:43:27.648Z