Crystallography Open Database
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Result: there are 16 entries in the selection
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Searching journal of publication like 'Chemical Communications (Cambridge, United Kingdom)' volume of publication is 46
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7105399 | CIF | C56 H40 Ho2 Na2 O16 | I 41 | 16.1249; 16.1249; 19.506 90; 90; 90 | 5071.8 | Majeed, Zeeshan; Mondal, Kartik C.; Kostakis, George E.; Lan, Yanhua; Anson, Christopher E.; Powell, Annie K. [LnNa(PhCO2)4] (Ln = Ho, Dy): the first examples of chiral srs 3D networks constructed using the monotopic benzoate ligand Chemical Communications (Cambridge, United Kingdom), 2010, 46, 2551-2553 |
| 7105400 | CIF | C56 H40 Dy2 Na2 O16 | I 41 | 16.1379; 16.1379; 19.5507 90; 90; 90 | 5091.6 | Majeed, Zeeshan; Mondal, Kartik C.; Kostakis, George E.; Lan, Yanhua; Anson, Christopher E.; Powell, Annie K. [LnNa(PhCO2)4] (Ln = Ho, Dy): the first examples of chiral srs 3D networks constructed using the monotopic benzoate ligand Chemical Communications (Cambridge, United Kingdom), 2010, 46, 2551-2553 |
| 7105401 | CIF | C16 H25 N O3 | P 1 21/c 1 | 5.811; 13.636; 21.023 90; 100.964; 90 | 1635.43 | Sonawane, Manoj R.; Císařová, Ivana; Lyapkalo, Ilya M. N-Trimethylsilyloxyenamines as new aldehyde enolate synthons: general, efficient and diastereoselective aldol reaction with ketals and acetals Chemical Communications (Cambridge, United Kingdom), 2010, 46, 2656-2658 |
| 7105402 | CIF | C21 H27 N O3 | P 1 21/c 1 | 16.1659; 5.6972; 20.6824 90; 90.5706; 90 | 1904.76 | Sonawane, Manoj R.; Císařová, Ivana; Lyapkalo, Ilya M. N-Trimethylsilyloxyenamines as new aldehyde enolate synthons: general, efficient and diastereoselective aldol reaction with ketals and acetals Chemical Communications (Cambridge, United Kingdom), 2010, 46, 2656-2658 |
| 7105403 | CIF | C16 H25 N O2 | P -1 | 5.9484; 8.4271; 15.9289 93.4557; 95.3665; 106.377 | 759.58 | Sonawane, Manoj R.; Císařová, Ivana; Lyapkalo, Ilya M. N-Trimethylsilyloxyenamines as new aldehyde enolate synthons: general, efficient and diastereoselective aldol reaction with ketals and acetals Chemical Communications (Cambridge, United Kingdom), 2010, 46, 2656-2658 |
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