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

Hongchang Qu; Michael D. Carducci; Gary S. Nichol; Victor J. Hruby

doi:10.1107/S1600536806032041

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

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

Chemistry & Biochemistry - Sci

Research output: Contribution to journal › Article › peer-review

Abstract

The title compound, C₂₅H₃₂N₂O₃, 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.

Original language	English (US)
Pages (from-to)	o3921-o3922
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	62
Issue number	9
DOIs	https://doi.org/10.1107/S1600536806032041
State	Published - Sep 2006

ASJC Scopus subject areas

General Chemistry
General Materials Science
Condensed Matter Physics

Access to Document

10.1107/S1600536806032041

Cite this

@article{f69f20f913824617b496c55eeb7b7d3d,

title = "(1R,2S)-Benzyl N-[3-(diisopropylamino-carbonyl)-2-phenylprop-3-enyl] carbamate",

abstract = "The title compound, C25H32N2O3, 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.",

author = "Hongchang Qu and Carducci, \{Michael D.\} and Nichol, \{Gary S.\} and Hruby, \{Victor J.\}",

year = "2006",

month = sep,

doi = "10.1107/S1600536806032041",

language = "English (US)",

volume = "62",

pages = "o3921--o3922",

journal = "Acta Crystallographica Section E: Structure Reports Online",

issn = "1600-5368",

publisher = "International Union of Crystallography",

number = "9",

}

TY - JOUR

T1 - (1R,2S)-Benzyl N-[3-(diisopropylamino-carbonyl)-2-phenylprop-3-enyl] carbamate

AU - Qu, Hongchang

AU - Carducci, Michael D.

AU - Nichol, Gary S.

AU - Hruby, Victor J.

PY - 2006/9

Y1 - 2006/9

N2 - The title compound, C25H32N2O3, 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.

AB - The title compound, C25H32N2O3, 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.

UR - https://www.scopus.com/pages/publications/33748560787

UR - https://www.scopus.com/pages/publications/33748560787#tab=citedBy

U2 - 10.1107/S1600536806032041

DO - 10.1107/S1600536806032041

M3 - Article

AN - SCOPUS:33748560787

SN - 1600-5368

VL - 62

SP - o3921-o3922

JO - Acta Crystallographica Section E: Structure Reports Online

JF - Acta Crystallographica Section E: Structure Reports Online

IS - 9

ER -

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

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this