Crystallography Open Database

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COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1506513 CIFC13 H16 Fe O SP 21 21 215.9295; 12.3312; 16.883
90; 90; 90		1234.4Fernández, Inmaculada; Valdivia, Victoria; Gori, Beatrice; Alcudia, Felipe; Alvarez, Eleuterio; Khiar, Noureddine
The isopropylsulfinyl group: a useful chiral controller for the asymmetric aziridination of sulfinylimines and the organocatalytic allylation of hydrazones.
Organic letters, 2005, 7, 1307-1310
1506514 CIFC20 H18P b c a10.7905; 7.675; 17.5436
90; 90; 90		1452.9Lunazzi, Lodovico; Mazzanti, Andrea; Minzoni, Mirko; Anderson, J. Edgar
Structure, conformation, and dynamic processes of the stereolabile atropisomers of hindered terphenyl hydrocarbons.
Organic letters, 2005, 7, 1291-1294
1506515 CIFC26 H30P 1 21/c 18.206; 19.137; 7.029
90; 108.955; 90		1044Lunazzi, Lodovico; Mazzanti, Andrea; Minzoni, Mirko; Anderson, J. Edgar
Structure, conformation, and dynamic processes of the stereolabile atropisomers of hindered terphenyl hydrocarbons.
Organic letters, 2005, 7, 1291-1294
1506516 CIFC14 H22 O2C 1 2/c 119.569; 9.6463; 15.091
90; 116.71; 90		2544.7Heim, Ralf; Wiedemann, Stefan; Williams, Craig M.; Bernhardt, Paul V.
Expedient construction of the vibsanin E core without the use of protecting groups.
Organic letters, 2005, 7, 1327-1329
1506517 CIFC16 H16 N2 O7P -18.3731; 14.2379; 15.576
115.671; 93.9504; 99.789		1627.87Ma, Cheng; Yang, Yewei
Thiazolium-mediated multicomponent reactions: a facile synthesis of 3-aminofuran derivatives.
Organic letters, 2005, 7, 1343-1345

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All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.