Crystallography Open Database

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Searching journal of publication like 'ACS combinatorial science' volume of publication is 14

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4505627 CIFC19 H17 F N2 O5P 1 21/c 18.3881; 11.532; 18.652
90; 97.916; 90
1787Tan, Darlene Q.; Atherton, Amy L.; Smith, Austin J.; Soldi, Cristian; Hurley, Katherine A.; Fettinger, James C.; Shaw, Jared T.
Synthesis of a γ-Lactam Library via Formal Cycloaddition of Imines and Substituted Succinic Anhydrides.
ACS combinatorial science, 2012, 14, 218-223
4505628 CIFC22 H26 F N3 O5P 1 21/c 113.4864; 20.1959; 16.1652
90; 90.179; 90
4402.9Tan, Darlene Q.; Atherton, Amy L.; Smith, Austin J.; Soldi, Cristian; Hurley, Katherine A.; Fettinger, James C.; Shaw, Jared T.
Synthesis of a γ-Lactam Library via Formal Cycloaddition of Imines and Substituted Succinic Anhydrides.
ACS combinatorial science, 2012, 14, 218-223
4505629 CIFC29 H26.33 Cl3.67 N4 O9P -17.7789; 13.1511; 16.1282
76.669; 84.6; 77.944
1568.2Tan, Darlene Q.; Atherton, Amy L.; Smith, Austin J.; Soldi, Cristian; Hurley, Katherine A.; Fettinger, James C.; Shaw, Jared T.
Synthesis of a γ-Lactam Library via Formal Cycloaddition of Imines and Substituted Succinic Anhydrides.
ACS combinatorial science, 2012, 14, 218-223
4505630 CIFC16 H12 N2 O S4P 1 21/c 18.6868; 12.061; 16.5857
90; 90.843; 90
1737.52Verma, Rajiv Kumar; Verma, Girijesh Kumar; Shukla, Gaurav; Nagaraju, Anugula; Singh, Maya Shankar
4-Dimethylamino Pyridine-Promoted One-Pot Three-Component Regioselective Synthesis of Highly Functionalized 4H-Thiopyrans via Heteroannulation of β-Oxodithioesters.
ACS combinatorial science, 2012, 14, 224-230
4506575 CIFC22 H17 N3 O2P 1 21/c 110.9445; 17.8505; 9.2774
90; 104.951; 90
1751.12Xu, Zhigang; Ayaz, Muhammad; Cappelli, Alexandra A.; Hulme, Christopher
General One-pot, Two-Step Protocol Accessing a Range of Novel Polycyclic Heterocycles with High Skeletal Diversity.
ACS combinatorial science, 2012, 14, 460-464
4506576 CIFC21 H19 F3 N4 O2P 1 21/c 113.1973; 14.8812; 10.1948
90; 110.978; 90
1869.47Xu, Zhigang; Ayaz, Muhammad; Cappelli, Alexandra A.; Hulme, Christopher
General One-pot, Two-Step Protocol Accessing a Range of Novel Polycyclic Heterocycles with High Skeletal Diversity.
ACS combinatorial science, 2012, 14, 460-464
4506577 CIFC19 H24 O3P 21 21 216.1622; 8.8128; 29.313
90; 90; 90
1591.9Xue, Wei-Jian; Li, Qi; Gao, Fang-Fang; Zhu, Yan-Ping; Wang, Jun-Gang; Zhang, Wei; Wu, An-Xin
Diversity-Oriented Synthesis of Chromenes via Metal-Free Domino Reactions from Ketones and Phenols.
ACS combinatorial science, 2012, 14, 478-483
4506578 CIFC15 H20 O3P b c a22.398; 15.1572; 23.824
90; 90; 90
8088Xue, Wei-Jian; Li, Qi; Gao, Fang-Fang; Zhu, Yan-Ping; Wang, Jun-Gang; Zhang, Wei; Wu, An-Xin
Diversity-Oriented Synthesis of Chromenes via Metal-Free Domino Reactions from Ketones and Phenols.
ACS combinatorial science, 2012, 14, 478-483
4506579 CIFC23 H18 Cl2 O3P 16.801; 8.232; 28.08
95.03; 90.61; 91.551
1565Xue, Wei-Jian; Li, Qi; Gao, Fang-Fang; Zhu, Yan-Ping; Wang, Jun-Gang; Zhang, Wei; Wu, An-Xin
Diversity-Oriented Synthesis of Chromenes via Metal-Free Domino Reactions from Ketones and Phenols.
ACS combinatorial science, 2012, 14, 478-483
4506580 CIFC23 H28 O6P 1 21/c 18.9227; 14.534; 15.883
90; 92.475; 90
2057.8Xue, Wei-Jian; Li, Qi; Gao, Fang-Fang; Zhu, Yan-Ping; Wang, Jun-Gang; Zhang, Wei; Wu, An-Xin
Diversity-Oriented Synthesis of Chromenes via Metal-Free Domino Reactions from Ketones and Phenols.
ACS combinatorial science, 2012, 14, 478-483
4506581 CIFC17 H24 O3P 1 21/n 18.362; 16.147; 11.767
90; 96.513; 90
1578.5Xue, Wei-Jian; Li, Qi; Gao, Fang-Fang; Zhu, Yan-Ping; Wang, Jun-Gang; Zhang, Wei; Wu, An-Xin
Diversity-Oriented Synthesis of Chromenes via Metal-Free Domino Reactions from Ketones and Phenols.
ACS combinatorial science, 2012, 14, 478-483
4507134 CIFC14 H16 Br N O3P 21 21 215.6996; 12.8774; 18.4471
90; 90; 90
1353.9Gerard, Baudouin; O'Shea, Morgan Welzel; Donckele, Etienne; Kesavan, Sarathy; Akella, Lakshmi B.; Xu, Hao; Jacobsen, Eric N.; Marcaurelle, Lisa A.
Application of a catalytic asymmetric Povarov reaction using chiral ureas to the synthesis of a tetrahydroquinoline library.
ACS combinatorial science, 2012, 14, 621-630

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