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Cho BR, Kim YK, Seung YJ, et al. Elimination reactions of aryl phenylacetates promoted by R(2)NH/R(2)NH(2)(+) in 70 mol MeCN(aq). Effect Of the beta-phenyl group on the ketene-forming transition state. J Org Chem. 2000;65(4):1239-42doi: 10.1021/jo991473v.
Cho, B. R., Kim, Y. K., Seung, Y. J., Kim, J. C., & Pyun, S. Y. (2000). Elimination reactions of aryl phenylacetates promoted by R(2)NH/R(2)NH(2)(+) in 70 mol MeCN(aq). Effect Of the beta-phenyl group on the ketene-forming transition state. The Journal of organic chemistry, 65(4), 1239-42. https://doi.org/10.1021/jo991473v
Cho, et al. "Elimination reactions of aryl phenylacetates promoted by R(2)NH/R(2)NH(2)(+) in 70 mol MeCN(aq). Effect Of the beta-phenyl group on the ketene-forming transition state." The Journal of organic chemistry vol. 65,4 (2000): 1239-42. doi: https://doi.org/10.1021/jo991473v
Cho BR, Kim YK, Seung YJ, Kim JC, Pyun SY. Elimination reactions of aryl phenylacetates promoted by R(2)NH/R(2)NH(2)(+) in 70 mol MeCN(aq). Effect Of the beta-phenyl group on the ketene-forming transition state. J Org Chem. 2000 Feb 25;65(4):1239-42. doi: 10.1021/jo991473v. PMID: 10814082.
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J Org Chem. 2000 Feb 25;65(4):1239-42. doi: 10.1021/jo991473v.

Elimination reactions of aryl phenylacetates promoted by R(2)NH/R(2)NH(2)(+) in 70 mol MeCN(aq). Effect Of the beta-phenyl group on the ketene-forming transition state.

The Journal of organic chemistry

Cho, Kim, Seung, Kim, Pyun

Affiliations

  1. Department of Chemistry, Division of Chemistry and Molecular Engineering, Korea University, 1-Anamdong, Seoul 136-701, and Department of Chemistry, Pukyong National University, Pusan 608-737, Korea.

PMID: 10814082 DOI: 10.1021/jo991473v

[No abstract available.]

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