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(1S,3S,4S)-tert-Butyl N-[1-benzyl-3-hydr-oxy-5-phenyl-4-(picolinamido)pent-yl]carbamate.

作者信息

Zheng Jian-Feng, Huang Su-Yu, Guo Jian-Nan, Zhang Yu, Jin Li-Ren

机构信息

Department of Chemistry and Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, People's Republic of China.

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2008 Jun 28;64(Pt 7):o1362. doi: 10.1107/S1600536808018965.

DOI:10.1107/S1600536808018965
PMID:21202980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2961835/
Abstract

The title compound, C(29)H(35)N(3)O(4), was obtained by the reaction of (2S,4S,5S)-tert-butyl N-(4-amino-1-benzyl-3-hydr-oxy-5-phenyl-pent-yl)carbamate and picolinic acid using oxalyl chloride as a chlorinating reagent to activate the carboxyl group. In the crystal structure there are two mol-ecules in the asymmetric unit, which are aligned edge-to-face. In one mol-ecule, the pyridyl ring forms a dihedral angle of 22.0 (1)° with the phenyl ring of the terminal benzyl group and 14.3 (1)° with the other phenyl ring; in the other mol-ecule, the corresponding angles are 12.1 (1) and 10.6 (1)°, respectively. The packing is stabilized by inter-molecular hydrogen bonds and C-H⋯π inter-actions.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c2/2961835/c3a9dbad081c/e-64-o1362-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c2/2961835/c3a9dbad081c/e-64-o1362-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8c2/2961835/c3a9dbad081c/e-64-o1362-fig2.jpg

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本文引用的文献

1
A short history of SHELX.SHELX简史。
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