Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 15
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1512336 | CIF | C26 H34 N2 O6 | P 1 21/c 1 | 9.8028; 17.9436; 14.8057 90; 108.059; 90 | 2476 | Mundal, Devon A.; Sarpong, Richmond Synthetic Studies toward the Citrinadin A and B Core Architecture. Organic letters, 2013, 15, 4952-4955 |
1512337 | CIF | C26 H34 N2 O5 | P -1 | 10.8816; 12.2655; 18.867 94.346; 106.589; 102.455 | 2331 | Mundal, Devon A.; Sarpong, Richmond Synthetic Studies toward the Citrinadin A and B Core Architecture. Organic letters, 2013, 15, 4952-4955 |
1512338 | CIF | C26 H32 N2 O5 | P 1 21/c 1 | 15.0275; 6.8288; 22.94 90; 90.555; 90 | 2353.99 | Mundal, Devon A.; Sarpong, Richmond Synthetic Studies toward the Citrinadin A and B Core Architecture. Organic letters, 2013, 15, 4952-4955 |
1512339 | CIF | C29 H45 N O5 S Si | P 1 21 1 | 7.9222; 9.853; 20.0514 90; 92.404; 90 | 1563.78 | Williams, Brett D.; Smith, 3rd, Amos B Total Synthesis of (+)-18-epi-Latrunculol A. Organic letters, 2013, 15, 4584-4587 |
1512340 | CIF | C36 H51 N O8 Se | P 21 21 21 | 12.1342; 12.8992; 22.5938 90; 90; 90 | 3536.4 | Gui, Jinghan; Tian, Hailong; Tian, Weisheng Synthesis of glaucogenin d, a structurally unique disecopregnane steroid with potential antiviral activity. Organic letters, 2013, 15, 4802-4805 |
1512341 | CIF | C23 H25 N O2 | P 1 21/c 1 | 11.319; 9.278; 18.4667 90; 94.237; 90 | 1934.03 | Liu, Xianglei; Ma, Xinna; Huang, Yunze; Gu, Zhenhua Pd-Catalyzed Heck-Type Cascade Reactions withN-Tosyl Hydrazones: An Efficient Way to Alkenes via in Situ Generated Alkylpalladium Organic Letters, 2013, 15, 4814 |
1512342 | CIF | C14 H15 N O3 | P 1 21/n 1 | 9.4301; 6.9967; 18.692 90; 96.925; 90 | 1224.3 | Gou, Quan; Deng, Bin; Zhang, Hongbin; Qin, Jun Arylations of Substituted Enamides by Aryl Iodides: Regio- and Stereoselective Synthesis of (Z)-β-Amido-β-Arylacrylates. Organic letters, 2013, 15, 4604-4607 |
1512343 | CIF | C14 H15 N O3 | P 1 21/n 1 | 9.5053; 14.4803; 9.8588 90; 108.461; 90 | 1287.1 | Gou, Quan; Deng, Bin; Zhang, Hongbin; Qin, Jun Arylations of Substituted Enamides by Aryl Iodides: Regio- and Stereoselective Synthesis of (Z)-β-Amido-β-Arylacrylates. Organic letters, 2013, 15, 4604-4607 |
1512344 | CIF | C12 H12 F N O3 | P 21 21 21 | 8.9371; 12.7168; 20.942 90; 90; 90 | 2380.1 | Gou, Quan; Deng, Bin; Zhang, Hongbin; Qin, Jun Arylations of Substituted Enamides by Aryl Iodides: Regio- and Stereoselective Synthesis of (Z)-β-Amido-β-Arylacrylates. Organic letters, 2013, 15, 4604-4607 |
1512345 | CIF | C20 H19 N3 O3 | P -1 | 8.05; 9.761; 11.482 76.232; 86.614; 78.203 | 857.7 | Zhang, Zhi-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui Cu(TFA)2-Catalyzed Oxidative Tandem Cyclization/1,2-Alkyl Migration of Enamino Amides for Synthesis of Pyrrolin-4-ones Organic Letters, 2013, 15, 4822 |
1512346 | CIF | C21 H24 Br N O3 | P 1 21 1 | 6.4311; 10.2155; 14.4708 90; 90.972; 90 | 950.55 | Fang, Li-Chao; Hsung, Richard P.; Ma, Zhi-Xiong; Presser, William R. A Highly Stereoselective Diels‒Alder Cycloaddition of Enones with Chiral Cyclic 2-Amidodienes Derived from Allenamides Organic Letters, 2013, 15, 4842 |
1512347 | CIF | C26 H27 N O3 | P 21 21 21 | 8.7711; 11.3886; 20.3871 90; 90; 90 | 2036.48 | Fang, Li-Chao; Hsung, Richard P.; Ma, Zhi-Xiong; Presser, William R. A Highly Stereoselective Diels‒Alder Cycloaddition of Enones with Chiral Cyclic 2-Amidodienes Derived from Allenamides Organic Letters, 2013, 15, 4842 |
1512348 | CIF | C21 H24 N2 O5 | P 21 21 2 | 11.3046; 26.6589; 6.2333 90; 90; 90 | 1878.5 | Fang, Li-Chao; Hsung, Richard P.; Ma, Zhi-Xiong; Presser, William R. A Highly Stereoselective Diels‒Alder Cycloaddition of Enones with Chiral Cyclic 2-Amidodienes Derived from Allenamides Organic Letters, 2013, 15, 4842 |
1512349 | CIF | C18 H18 N2 O4 | P 1 21/c 1 | 10.218; 17.627; 18.0314 90; 97.932; 90 | 3216.6 | Lin, Wen-Chung; Yang, Ding-Yah Visible Light Photoredox Catalysis: Synthesis of Indazolo[2,3-a]quinolines from 2-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolines Organic Letters, 2013, 15, 4862 |
1512350 | CIF | C19 H20 N2 O4 | P -1 | 8.4406; 10.2459; 10.6103 66.366; 80.901; 74.929 | 810.21 | Lin, Wen-Chung; Yang, Ding-Yah Visible Light Photoredox Catalysis: Synthesis of Indazolo[2,3-a]quinolines from 2-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolines Organic Letters, 2013, 15, 4862 |
1512351 | CIF | C18 H18 N2 O3 | P -1 | 8.2315; 10.0246; 10.7097 115.321; 94.926; 105.247 | 750.52 | Lin, Wen-Chung; Yang, Ding-Yah Visible Light Photoredox Catalysis: Synthesis of Indazolo[2,3-a]quinolines from 2-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolines Organic Letters, 2013, 15, 4862 |
1512352 | CIF | C20 H21 N3 O4 | P -1 | 9.2372; 9.6199; 10.3333 83.624; 76.161; 82.285 | 880.52 | Lin, Wen-Chung; Yang, Ding-Yah Visible Light Photoredox Catalysis: Synthesis of Indazolo[2,3-a]quinolines from 2-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolines Organic Letters, 2013, 15, 4862 |
1512353 | CIF | C18 H16 N2 O2 | P -1 | 8.2451; 9.8764; 10.1747 99.779; 110.657; 106.935 | 706.43 | Lin, Wen-Chung; Yang, Ding-Yah Visible Light Photoredox Catalysis: Synthesis of Indazolo[2,3-a]quinolines from 2-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolines Organic Letters, 2013, 15, 4862 |
1512354 | CIF | C18 H18 N2 O2 | P b c a | 11.3182; 15.2662; 16.9741 90; 90; 90 | 2932.9 | Lin, Wen-Chung; Yang, Ding-Yah Visible Light Photoredox Catalysis: Synthesis of Indazolo[2,3-a]quinolines from 2-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolines Organic Letters, 2013, 15, 4862 |
1512355 | CIF | C21 H18 N2 O | P 1 21/n 1 | 9.8799; 11.9219; 13.6695 90; 91.371; 90 | 1609.63 | Lin, Wen-Chung; Yang, Ding-Yah Visible Light Photoredox Catalysis: Synthesis of Indazolo[2,3-a]quinolines from 2-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolines Organic Letters, 2013, 15, 4862 |
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