1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a'-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one-Reference-Cited by-同舟云学术

1′,5-Dinitro-2′-phenyl-2′,3′,5′,6′,7′,7a'-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one

Published:2008-08-13 Issue:9 Volume:64 Page:o1740-o1740
ISSN:1600-5368
Container-title:Acta Crystallographica Section E Structure Reports Online
language:
Short-container-title:Acta Cryst E

Author:

Sarrafi Yaghoub,Alimohammadi Kamal

Abstract

In the title cycloadduct, C20H18N4O5, the rings of the pyrrolizine system adopt envelope conformations. A centrosymmetric dimer is formed via intermolecular N—H...O hydrogen bonds between the indolinone rings.

Publisher

International Union of Crystallography (IUCr)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://journals.iucr.org/e/issues/2008/09/00/om2253/om2253.pdf

Reference9 articles.

1. Bruker (2007). SMART and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.

2. Reaction between proline and γ-oxo α,β-unsaturated esters: new access to polysubstituted pyrrolizidines

3. 2-Oxoindolin-3-ylidene derivatives as 2π components in 1,3-dipolar cycloadditions of azomethine ylides

4. Diastereoselective syntheses of pyrazolyl isoxazolidines via 1,3-dipolar cycloaddition

5. Pyrrolizidine alkaloids

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1. Regio- and stereospecific assembly of dispiro[indoline-3,3′-pyrrolizine-1′,5′′-thiazolidines] from simple precursors using a one-pot procedure: synthesis, spectroscopic and structural characterization, and a proposed mechanism of formation;Acta Crystallographica Section C Structural Chemistry;2020-07-22

2. Synthesis of spiro[indoline-3,3′-pyrrolizines] by 1,3-dipolar reactions between isatins, L-proline and electron-deficient alkenes;Acta Crystallographica Section C Structural Chemistry;2017-11-13