Crystal structure of (Z)-3-(6-bromo-1H-indol-3-yl)-1,3-diphenylprop-2-en-1-one, C23H16BrNO-Reference-Cited by-同舟云学术

Crystal structure of (Z)-3-(6-bromo-1H-indol-3-yl)-1,3-diphenylprop-2-en-1-one, C23H16BrNO

Published:2020-12-10 Issue:2 Volume:236 Page:305-306
ISSN:2197-4578
Container-title:Zeitschrift für Kristallographie - New Crystal Structures
language:en
Short-container-title:

Author:

Pan Fei¹,Wei Xian¹,Lv Menglan Lan¹^ORCID

Affiliation:

1. School of Chemical Engineering, Guizhou Institute of Technology , Guizhou , 550003, P.R. China

Abstract

Abstract C23H16BrNO, triclinic, P 1 ‾

$P‾{1}$

(no. 2), a = 9.914(3) Å, b = 10.141(3) Å, c = 10.179(3) Å, α = 90.177(5)°, β = 112.202(5)°, γ = 95.167(5)°, V = 942.9(4) Å3, Z = 2, R gt (F) = 0.0520, wR ref (F 2) = 0.1351, T = 296 K. CCDC no.: 2043972

Funder

Natural Science Foundation of China

Excellent Young Scientific and Technological Talents of Guizhou, China

Publisher

Walter de Gruyter GmbH

Subject

Inorganic Chemistry,Condensed Matter Physics,General Materials Science

Link

https://www.degruyter.com/document/doi/10.1515/ncrs-2020-0533/pdf

Reference7 articles.

1. Bruker. SAINT. APEX2 and SADABS; Bruker AXS Inc.: Madison, Wisconsin, USA, 2009.

2. Sheldrick, G. M. Crystal structure refinement with SHELXL. Acta Crystallogr. 2015, C71, 3–8; https://doi.org/10.1107/s2053229614024218.

3. Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K., Puschmann, H. OLEX2: a complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 2009, 42, 339–341; https://doi.org/10.1107/s0021889808042726.

4. Chen, Z. Z., Li, S. Q., Zhang, Y. J., Tang, D. Y., Meng, J. P., Lei, J., Li, H. Y., Xu, Z. G. Synthesis of pyridodiindoles with anticancer activity by a three-component cascade condensation. Org. Lett. 2018, 20, 7811–7815; https://doi.org/10.1021/acs.orglett.8b03245.

5. Li, Y., Meng, J. P., Lei, J., Chen, Z. Z., Tang, D. Y., Zhu, J., Zhang, J., Xu, Z. G. Efficient synthesis of fused oxazepino-isoquinoline scaffolds via an Ugi, followed by an intramolecular cyclization. ACS Comb. Sci. 2017, 19, 324–330; https://doi.org/10.1021/acscombsci.7b00002.