论文信息 - 1′‐Phenyl‐2′,3′,5′,6′,7′,7a′‐hexahydroindan‐2‐spiro‐2′‐1H‐pyrrolizine‐3′‐spiro‐11′‐indeno[1,2‐b]quinoxaline‐1,3‐dione. Corrigendum - 字舞流文

1′‐Phenyl‐2′,3′,5′,6′,7′,7a′‐hexahydroindan‐2‐spiro‐2′‐1H‐pyrrolizine‐3′‐spiro‐11′‐indeno[1,2‐b]quinoxaline‐1,3‐dione. Corrigendum

In the paper by Gayathri, Aravindan, Velmurugan, Ravikumar & Sureshbabu [Acta Cryst. (2005), E61, o3124–o3126], the formula is given incorrectly in the Abstract. The correct formula is C35H25N3O2.

P. G. Aravindan | D. Velmurugan | D. Gayathri | K. Ravikumar | A. R. Sureshbabu

[1] Antonios Kolocouris,et al. Spiro[pyrrolidine-2,2'-adamantanes]: synthesis, anti-influenza virus activity and conformational properties. , 2003, Bioorganic & medicinal chemistry letters.

[2] A. A. Raj,et al. Synthesis, antimicrobial and antifungal activity of a new class of spiro pyrrolidines. , 2003, Bioorganic & medicinal chemistry.

[3] A. Zagórska,et al. Synthesis and anticonvulsant properties of new 1-phenyl and 1-phenylamino-3-phenylpyrrolidine-2,5-dione derivatives. , 2002, Acta poloniae pharmaceutica.

[4] M. Nardelli,et al. PARST95 – an update to PARST: a system of Fortran routines for calculating molecular structure parameters from the results of crystal structure analyses , 1995 .

[5] Raymond E. Davis,et al. Patterns in Hydrogen Bonding: Functionality and Graph Set Analysis in Crystals , 1995 .

[6] D. Cremer,et al. General definition of ring puckering coordinates , 1975 .

[7] A. Monge,et al. Synthesis and antimycobacterial activity of new quinoxaline-2-carboxamide 1,4-di-N-oxide derivatives. , 2003, Bioorganic & medicinal chemistry.