Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II.

Kumar P, Dubey A, Harbindu A

Open source

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

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