trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate

The title compound, C(21)H(23)NO(7)S, is an important inter­mediate in the synthesis of poly(amido­amine) dendrimers. The cyclo­hexane ring adopts a chair conformation. The dihedral angle between the two aromatic rings is 69.5 (2)°. The mol­ecules are linked into a zigzag chain along the b axis by C...

Descripción completa

Detalles Bibliográficos
Autores principales: Qi, Qing-Rong, Huang, Wen-Cai, Mao, Zhi-Hua, Zheng, Hu
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960325/
https://www.ncbi.nlm.nih.gov/pubmed/21201415
http://dx.doi.org/10.1107/S1600536808000068
_version_ 1782188712353857536
author Qi, Qing-Rong
Huang, Wen-Cai
Mao, Zhi-Hua
Zheng, Hu
author_facet Qi, Qing-Rong
Huang, Wen-Cai
Mao, Zhi-Hua
Zheng, Hu
author_sort Qi, Qing-Rong
collection PubMed
description The title compound, C(21)H(23)NO(7)S, is an important inter­mediate in the synthesis of poly(amido­amine) dendrimers. The cyclo­hexane ring adopts a chair conformation. The dihedral angle between the two aromatic rings is 69.5 (2)°. The mol­ecules are linked into a zigzag chain along the b axis by C—H⋯O hydrogen bonds.
format Text
id pubmed-2960325
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29603252010-12-30 trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate Qi, Qing-Rong Huang, Wen-Cai Mao, Zhi-Hua Zheng, Hu Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(23)NO(7)S, is an important inter­mediate in the synthesis of poly(amido­amine) dendrimers. The cyclo­hexane ring adopts a chair conformation. The dihedral angle between the two aromatic rings is 69.5 (2)°. The mol­ecules are linked into a zigzag chain along the b axis by C—H⋯O hydrogen bonds. International Union of Crystallography 2008-01-09 /pmc/articles/PMC2960325/ /pubmed/21201415 http://dx.doi.org/10.1107/S1600536808000068 Text en © Qi et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Qi, Qing-Rong
Huang, Wen-Cai
Mao, Zhi-Hua
Zheng, Hu
trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate
title trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate
title_full trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate
title_fullStr trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate
title_full_unstemmed trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate
title_short trans-4-Nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate
title_sort trans-4-nitro­phenyl 4-(tosyl­oxymeth­yl)cyclo­hexa­necarboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960325/
https://www.ncbi.nlm.nih.gov/pubmed/21201415
http://dx.doi.org/10.1107/S1600536808000068
work_keys_str_mv AT qiqingrong trans4nitrophenyl4tosyloxymethylcyclohexanecarboxylate
AT huangwencai trans4nitrophenyl4tosyloxymethylcyclohexanecarboxylate
AT maozhihua trans4nitrophenyl4tosyloxymethylcyclohexanecarboxylate
AT zhenghu trans4nitrophenyl4tosyloxymethylcyclohexanecarboxylate

Ejemplares similares