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Qu H, Carducci MD, Nichol GS, et al. (1R,2S)-Benzyl N-[3-(diisopropylaminocarbonyl)-2-phenylprop-3-enyl]carbamate. Acta Crystallogr Sect E Struct Rep Online. 2006;62(9):o3921-o3922doi: 10.1107/S1600536806032041.
Qu, H., Carducci, M. D., Nichol, G. S., & Hruby, V. J. (2006). (1R,2S)-Benzyl N-[3-(diisopropylaminocarbonyl)-2-phenylprop-3-enyl]carbamate. Acta crystallographica. Section E, Structure reports online, 62(9), o3921-o3922. https://doi.org/10.1107/S1600536806032041
Qu, Hongchang, et al. "(1R,2S)-Benzyl N-[3-(diisopropylaminocarbonyl)-2-phenylprop-3-enyl]carbamate." Acta crystallographica. Section E, Structure reports online vol. 62,9 (2006): o3921-o3922. doi: https://doi.org/10.1107/S1600536806032041
Qu H, Carducci MD, Nichol GS, Hruby VJ. (1R,2S)-Benzyl N-[3-(diisopropylaminocarbonyl)-2-phenylprop-3-enyl]carbamate. Acta Crystallogr Sect E Struct Rep Online. 2006 Sep;62(9):o3921-o3922. doi: 10.1107/S1600536806032041. PMID: 17710225; PMCID: PMC1950127.
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Acta Crystallogr Sect E Struct Rep Online. 2006 Sep;62(9):o3921-o3922. doi: 10.1107/S1600536806032041.

(1R,2S)-Benzyl N-[3-(diisopropylaminocarbonyl)-2-phenylprop-3-enyl]carbamate.

Acta crystallographica. Section E, Structure reports online

Hongchang Qu, Michael D Carducci, Gary S Nichol, Victor J Hruby

Affiliations

  1. Department of Chemistry, The University of Arizona, 1306 E University Boulevard, Tucson, AZ 85721, USA.

PMID: 17710225 PMCID: PMC1950127 DOI: 10.1107/S1600536806032041

Abstract

The title compound, C(25)H(32)N(2)O(3), was synthesized as part of a series of related compounds using a modified Eschenmoser-Claisen rearrangement reaction. The compound is racemic and the structure features a centrosymmetric hydrogen-bonded dimerization along with some aromatic stacking stabilization.

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