Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 17
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1520309 | CIF | C12 H18 B F2 N O3 | P 1 21 1 | 14.7772; 11.1085; 16.6848 90; 92.405; 90 | 2736.4 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520310 | CIF | C13 H20 B F2 N O3 | P 1 21/n 1 | 10.6399; 11.8723; 11.9174 90; 107.028; 90 | 1439.41 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520311 | CIF | C12 H18 B F2 N O4 | P -1 | 11.3963; 11.7254; 12.5468 74.986; 64.116; 64.237 | 1353.47 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520312 | CIF | C10 H16 B F2 N O4 | I b a 2 | 12.1721; 49.556; 8.341 90; 90; 90 | 5031.3 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520313 | CIF | C10 H16 B F2 N O4 | P -1 | 7.0022; 7.7079; 12.3657 83.232; 83.476; 76.265 | 641.26 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520314 | CIF | C10 H17 N O4 | P -1 | 7.8792; 8.1476; 10.2749 106.191; 106.585; 104.538 | 566.58 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520315 | CIF | C12 H20 B F2 N O4 | P b c a | 16.8311; 9.1985; 18.0999 90; 90; 90 | 2802.24 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520316 | CIF | C12 H18 B Br2 F2 N O4 | P 1 21/c 1 | 10.3517; 15.7916; 9.5485 90; 99.476; 90 | 1539.59 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520317 | CIF | C8 H11 Br O4 | P 1 21/c 1 | 8.8688; 18.0772; 6.0396 90; 94.753; 90 | 964.96 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520318 | CIF | C19 H23.6 B F2 N2 O5.3 | P b c n | 12.2584; 10.1061; 31.0115 90; 90; 90 | 3841.8 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520319 | CIF | C19 H23 B F2 N2 O5 | P 1 21/n 1 | 15.4609; 8.0727; 15.6576 90; 103.611; 90 | 1899.36 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520320 | CIF | C30 H25 N2 O4 P | P 1 21/c 1 | 12.5638; 14.8917; 13.7164 90; 104.477; 90 | 2484.8 | Yamamura, Masaki; Takizawa, Hiroyuki; Nabeshima, Tatsuya Zwitterionic N2O2-Type Protonated Dipyrrin Bearing a Phosphate Anionic Moiety as a pH-Responsive Fluorescence Indicator. Organic letters, 2015, 17, 3114-3117 |
1520385 | CIF | C41 H45 Cl2 N5 O18 | P -1 | 18.718; 20.1801; 21.555 63.466; 65.8; 82.646 | 6629.1 | Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K. β-Decamethoxysapphyrin and Its N-Benzyl Analogue. Organic letters, 2015, 17, 3030-3033 |
1520386 | CIF | C48 H53 N5 O16 S2 | P 1 21/n 1 | 9.5948; 11.7166; 43.6295 90; 91.392; 90 | 4903.3 | Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K. β-Decamethoxysapphyrin and Its N-Benzyl Analogue. Organic letters, 2015, 17, 3030-3033 |
1520387 | CIF | C48 H51 N5 O13 S | P 1 21/c 1 | 10.656; 38.925; 11.435 90; 111.21; 90 | 4422 | Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K. β-Decamethoxysapphyrin and Its N-Benzyl Analogue. Organic letters, 2015, 17, 3030-3033 |
1520388 | CIF | C22 H19 N O2 | P 21 21 21 | 8.6008; 10.6881; 18.1 90; 90; 90 | 1663.9 | Battini, Narsaiah; Battula, Satyanarayana; Kumar, Raju Ranjith; Ahmed, Qazi Naveed 2-Oxo Driven Unconventional reactions: Microwave Assisted Approaches to Tetrahydrofuro[3,2-d]oxazoles and Furanones. Organic letters, 2015, 17, 2992-2995 |
1520439 | CIF | C26 H18 B Cl2 F8 N3 | P 1 21/c 1 | 7.923; 11.039; 27.77 90; 96.981; 90 | 2410.8 | Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties. Organic letters, 2015, 17, 3090-3093 |
1520440 | CIF | C26.14 H22.79 B Cl0.79 F2 N3 O3.24 | P 1 21/c 1 | 13.159; 12.065; 15.082 90; 98.075; 90 | 2370.7 | Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties. Organic letters, 2015, 17, 3090-3093 |
1520441 | CIF | C707 H656 B16 F32 N48 O9 | P 1 21/c 1 | 15.429; 41.602; 24.49 90; 91.209; 90 | 15716 | Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties. Organic letters, 2015, 17, 3090-3093 |
1520442 | CIF | C35.79 H27.57 B Cl1.57 F2 N3 | C 1 2/c 1 | 33.021; 10.588; 23.034 90; 132.89; 90 | 5900 | Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties. Organic letters, 2015, 17, 3090-3093 |
1520443 | CIF | C32 H24 B Cl2 F2 N3 | P -1 | 7.3425; 11.0127; 15.884 94.772; 97.467; 91.375 | 1268.3 | Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties. Organic letters, 2015, 17, 3090-3093 |
1520444 | CIF | C50.45 H44.9 B Cl2.9 F2 N3 | P 1 21/c 1 | 8.0911; 21.853; 25.007 90; 97.291; 90 | 4385.9 | Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties. Organic letters, 2015, 17, 3090-3093 |
1520445 | CIF | C23 H18 B F2 N3 | P 1 21/n 1 | 9.594; 8.7428; 21.526 90; 100.795; 90 | 1773.6 | Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties. Organic letters, 2015, 17, 3090-3093 |
1520446 | CIF | C16 H15 N O2 S2 | P c a 21 | 18.773; 7.8448; 20.3148 90; 90; 90 | 2991.8 | Siva Reddy, Alla; Kumara Swamy, K. C. Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams. Organic letters, 2015, 17, 2996-2999 |
1520447 | CIF | C16 H14 F N O2 S2 | P 1 21/c 1 | 15.7817; 13.0488; 7.2719 90; 92.391; 90 | 1496.2 | Siva Reddy, Alla; Kumara Swamy, K. C. Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams. Organic letters, 2015, 17, 2996-2999 |
1520448 | CIF | C16 H15 N O3 S2 | P -1 | 9.7686; 10.4236; 16.0412 90.974; 91.846; 107.681 | 1554.8 | Siva Reddy, Alla; Kumara Swamy, K. C. Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams. Organic letters, 2015, 17, 2996-2999 |
1520449 | CIF | C16 H15 N O2 S Se | P b c a | 7.38023; 12.875; 31.8273 90; 90; 90 | 3024.24 | Siva Reddy, Alla; Kumara Swamy, K. C. Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams. Organic letters, 2015, 17, 2996-2999 |
1520450 | CIF | C17 H17 N O2 S2 | P 1 21/n 1 | 6.63588; 12.9255; 19.0476 90; 93.665; 90 | 1630.41 | Siva Reddy, Alla; Kumara Swamy, K. C. Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams. Organic letters, 2015, 17, 2996-2999 |
1520451 | CIF | C40 H32 N2 | P 1 21/n 1 | 12.149; 7.34; 16.53 90; 101.456; 90 | 1444.7 | Xu, Feng; Peng, Lifen; Shinohara, Kenta; Nishida, Takanori; Wakamatsu, Kan; Uejima, Motoyuki; Sato, Tohru; Tanaka, Kazuyoshi; Machida, Norihiko; Akashi, Haruo; Orita, Akihiro; Otera, Junzo One-Shot Double Amination of Sondheimer-Wong Diynes: Synthesis of Photoluminescent Dinaphthopentalenes. Organic letters, 2015, 17, 3014-3017 |
1520491 | CIF | C60 H74 N4 O4 | P -1 | 11.2497; 12.373; 20.0241 95.185; 106.067; 94.622 | 2651.1 | Xia, Debin; Marszalek, Tomasz; Li, Mengmeng; Guo, Xin; Baumgarten, Martin; Pisula, Wojciech; Müllen, Klaus Solution-Processable n-Type Organic Semiconductors Based on Angular-Shaped 2-(12H-Dibenzofluoren-12-ylidene)malononitrilediimide. Organic letters, 2015, 17, 3074-3077 |
1520504 | CIF | C20 H16 I N O | P -1 | 10.699; 11.726; 22.2683 94.284; 101.795; 109.369 | 2549 | Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization. Organic letters, 2015, 17, 3186-3189 |
1520505 | CIF | C20 H16 I N O | P b c a | 7.2355; 20.9295; 23.0167 90; 90; 90 | 3485.5 | Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization. Organic letters, 2015, 17, 3186-3189 |
1520513 | CIF | C24 H24 | P 1 21/n 1 | 7.4014; 30.606; 7.739 90; 100.806; 90 | 1722 | Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones. Organic letters, 2015, 17, 3142-3145 |
1520514 | CIF | C20 H24 O4 S | P 1 n 1 | 11.2988; 5.7063; 14.045 90; 102.129; 90 | 885.3 | Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones. Organic letters, 2015, 17, 3142-3145 |
1520515 | CIF | C25 H29 N O5 S | F d d 2 | 22.419; 52.094; 7.523 90; 90; 90 | 8786 | Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones. Organic letters, 2015, 17, 3142-3145 |
1520516 | CIF | C25 H29 N O5 S | C 1 2/c 1 | 30.166; 11.6914; 14.2065 90; 113.297; 90 | 4601.9 | Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones. Organic letters, 2015, 17, 3142-3145 |
1520517 | CIF | C19 H19 F O | P 21 21 21 | 8.4903; 9.6656; 18.663 90; 90; 90 | 1531.6 | Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones. Organic letters, 2015, 17, 3142-3145 |
1520518 | CIF | C43 H41 N3 O4 | P 1 21/c 1 | 31.617; 15.428; 14.478 90; 101.899; 90 | 6910 | Zhang, Feng-Lian; Zhu, Xu; Chiba, Shunsuke Tf~2~NH-Catalyzed Amide Synthesis from Vinyl Azides and Alcohols Organic Letters, 2015, 17, 3138-3141 |
1520519 | CIF | C13 H12 Cl N O4 | P 21 21 21 | 7.9023; 12.49; 12.9 90; 90; 90 | 1273.2 | Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo Catalytic Activity of epi-Quinine-Derived 3,5-Bis(trifluoromethyl)benzamide in Asymmetric Nitro-Michael Reaction of Furanones. Organic letters, 2015, 17, 3026-3029 |
1520520 | CIF | C39 H40 B F2 N3 O4 | P -1 | 8.745; 10.225; 20.19 89.48; 86.38; 65.669 | 1641.4 | Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene. Organic letters, 2015, 17, 3022-3025 |
1520521 | CIF | C37.5 H36.5 B Cl1.5 F2 N3 O4 | P -1 | 8.776; 10.567; 19.225 84.193; 82.204; 69.585 | 1652.6 | Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene. Organic letters, 2015, 17, 3022-3025 |
1520522 | CIF | C46 H44 B2 N2 O2 | P 1 21/c 1 | 7.274; 17.864; 15.322 90; 100.332; 90 | 1958.7 | Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures. Organic letters, 2015, 17, 3174-3177 |
1520523 | CIF | C42 H36 B2 N2 O2 | P 1 21/c 1 | 7.054; 17.672; 13.751 90; 96.406; 90 | 1703.5 | Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures. Organic letters, 2015, 17, 3174-3177 |
1520542 | CIF | C32 H25 N O4 | P 1 21 1 | 6.62144; 20.1343; 9.362 90; 100.915; 90 | 1225.54 | Zhao, Shuai; Zhao, Yuan-Yuan; Lin, Jun-Bing; Xie, Ting; Liang, Yong-Min; Xu, Peng-Fei Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives. Organic letters, 2015, 17, 3206-3209 |
1520547 | CIF | C25 H24 S | P -1 | 9.4128; 9.6074; 12.0794 97.999; 97.992; 108.357 | 1007.08 | Zhang, Hang; Wang, Bo; Yi, Heng; Zhang, Yan; Wang, Jianbo Rh(II)-Catalyzed [2,3]-Sigmatropic Rearrangement of Sulfur Ylides Derived from Cyclopropenes and Sulfides. Organic letters, 2015, 17, 3322-3325 |
1520552 | CIF | C36 H22 N12 | P 1 21/n 1 | 15.3809; 11.5149; 17.7975 90; 90.677; 90 | 3151.9 | Saltsman, Irena; Goldberg, Israel; Gross, Zeev Porphyrins and Corroles with 2,6-Pyrimidyl Substituents. Organic letters, 2015, 17, 3214-3217 |
1520553 | CIF | C35 H19 F4 N6 O2 P | I b a 2 | 21.689; 29.869; 10.7143 90; 90; 90 | 6941 | Saltsman, Irena; Goldberg, Israel; Gross, Zeev Porphyrins and Corroles with 2,6-Pyrimidyl Substituents. Organic letters, 2015, 17, 3214-3217 |
1520554 | CIF | C51 H33 Co F4 N8 | P 1 21/c 1 | 12.3996; 15.4999; 21.5037 90; 97.248; 90 | 4099.8 | Saltsman, Irena; Goldberg, Israel; Gross, Zeev Porphyrins and Corroles with 2,6-Pyrimidyl Substituents. Organic letters, 2015, 17, 3214-3217 |
1520555 | CIF | C24 H20 Br2 N2 | C 1 2/c 1 | 16.3504; 14.9527; 9.2389 90; 92.387; 90 | 2256.8 | Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R. Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly. Organic letters, 2015, 17, 3233-3235 |
1520556 | CIF | C24 H18 N2 | P -1 | 9.4274; 12.3411; 15.5934 83.302; 82.714; 79.24 | 1759.9 | Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R. Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly. Organic letters, 2015, 17, 3233-3235 |
1520557 | CIF | C62 H50 Ag2 N4 O6 S2 | P 1 21/c 1 | 14.33; 10.8862; 17.8919 90; 110.048; 90 | 2622 | Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R. Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly. Organic letters, 2015, 17, 3233-3235 |
1520558 | CIF | C50 H36 Ag2 F6 N4 O6 S2 | P -1 | 10.3809; 10.9748; 11.0438 109.43; 98.185; 97.328 | 1153.7 | Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R. Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly. Organic letters, 2015, 17, 3233-3235 |
1520559 | CIF | C50 H36 Ag2 F6 N4 O6 S2 | P -1 | 10.4495; 11.0503; 11.0576 109.671; 96.586; 97.962 | 1172.8 | Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R. Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly. Organic letters, 2015, 17, 3233-3235 |
1520560 | CIF | C62 H50 Ag2 N4 O6 S2 | P 1 21/c 1 | 14.369; 10.925; 18.106 90; 110.574; 90 | 2661 | Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R. Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly. Organic letters, 2015, 17, 3233-3235 |
1520561 | CIF | C51 H58 F6 O14 S2 | P -1 | 11.2709; 11.7647; 20.1194 88.271; 83.035; 86.352 | 2642.1 | Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives. Organic letters, 2015, 17, 3260-3263 |
1520562 | CIF | C46 H46 Cl2 F6 O14 S2 | P 1 n 1 | 11.616; 18.2419; 11.617 90; 94.1589; 90 | 2455.14 | Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives. Organic letters, 2015, 17, 3260-3263 |
1520563 | CIF | C48.75 H55.04 Cl2.25 F3 O12 S | P n a 21 | 35.9931; 12.0648; 11.369 90; 90; 90 | 4937 | Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives. Organic letters, 2015, 17, 3260-3263 |
1520564 | CIF | C51 H58 F6 O14 S2 | P 21 21 21 | 11.3045; 12.1357; 37.187 90; 90; 90 | 5101.6 | Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives. Organic letters, 2015, 17, 3260-3263 |
1520565 | CIF | C51 H55 F9 O16 S3 | P 1 21/c 1 | 22.0373; 11.9982; 22.7155 90; 110.288; 90 | 5633.5 | Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives. Organic letters, 2015, 17, 3260-3263 |
1520566 | CIF | C51 H55 F9 O16 S3 | P b c a | 20.6289; 22.2856; 24.1696 90; 90; 90 | 11111.4 | Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives. Organic letters, 2015, 17, 3260-3263 |
1520573 | CIF | C17 H15 N S | P 21 21 21 | 6.1669; 12.182; 17.8605 90; 90; 90 | 1341.77 | Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J. Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation. Organic letters, 2015, 17, 3222-3225 |
1520574 | CIF | C19 H17 N O | P b c a | 7.4565; 18.3137; 20.6855 90; 90; 90 | 2824.73 | Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J. Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation. Organic letters, 2015, 17, 3222-3225 |
1520575 | CIF | C16 H15 N3 | P 1 21/m 1 | 9.7773; 6.90436; 9.79548 90; 98.985; 90 | 653.14 | Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines. Organic letters, 2015, 17, 3374-3377 |
1520576 | CIF | C21 H15 N3 | P 1 21/c 1 | 14.0946; 11.4421; 9.74761 90; 99.2056; 90 | 1551.77 | Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines. Organic letters, 2015, 17, 3374-3377 |
1520577 | CIF | C20 H20 O6 | P 21 21 21 | 10.1756; 12.2477; 13.4918 90; 90; 90 | 1681.45 | Bautista, Elihú; Fragoso-Serrano, Mabel; Toscano, Rubén A; García-Peña, María Del Rosario; Ortega, Alfredo Teotihuacanin, a Diterpene with an Unusual Spiro-10/6 System from Salvia amarissima with Potent Modulatory Activity of Multidrug Resistance in Cancer Cells. Organic letters, 2015, 17, 3280-3282 |
1520614 | CIF | C25 H23 N O3 | P 1 21/c 1 | 9.4141; 23.293; 9.0609 90; 92.942; 90 | 1984.3 | Brady, Patrick B.; Carreira, Erick M. Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles. Organic letters, 2015, 17, 3350-3353 |
1520615 | CIF | C18 H17 N O2 | P 1 21/c 1 | 8.0166; 15.8594; 11.2674 90; 98.788; 90 | 1415.7 | Brady, Patrick B.; Carreira, Erick M. Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles. Organic letters, 2015, 17, 3350-3353 |
1520616 | CIF | C37 H31 N O5 | P 1 21/n 1 | 11.364; 10.93; 24.447 90; 96.564; 90 | 3017 | Mo, Lei; Wu, Lin-Lin; Wang, Shaozhong; Yao, Zhu-Jun Efficient Synthesis of Octahydrophenanthrene Derivatives with Mild Cascade Reactions of Isochromenylium Tetrafluoroborates and Bifunctional Styrenes. Organic letters, 2015, 17, 3314-3317 |
1520633 | CIF | C22 H21 Br N2 O3 S2 | P b c a | 11.7745; 15.3391; 24.3582 90; 90; 90 | 4399.34 | Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines. Organic letters, 2015, 17, 3330-3333 |
1520634 | CIF | C22 H20 N2 O4 S2 | P -1 | 9.0038; 10.66; 11.8108 75.2664; 76.0323; 75.5364 | 1042.26 | Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines. Organic letters, 2015, 17, 3330-3333 |
1520635 | CIF | C30 H29 N O3 | P 21 21 21 | 7.37176; 14.7771; 21.8173 90; 90; 90 | 2376.63 | Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides. Organic letters, 2015, 17, 3362-3365 |
1520636 | CIF | C29 H32 N2 S2 | P 1 21 1 | 10.39896; 9.11807; 13.7409 90; 108.291; 90 | 1237.06 | Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides. Organic letters, 2015, 17, 3362-3365 |
1520637 | CIF | C21 H15 F O2 | P 1 21/c 1 | 12.0845; 5.9453; 22.597 90; 103.246; 90 | 1580.3 | Du, Xiang-Wei; Stanley, Levi M. Tandem Alkyne Hydroacylation and Oxo-Michael Addition: Diastereoselective Synthesis of 2,3-Disubstituted Chroman-4-ones and Fluorinated Derivatives. Organic letters, 2015, 17, 3276-3279 |
1520655 | CIF | C32 H38 O5 Si2 | P 1 21/c 1 | 9.2692; 9.7098; 34.752 90; 92.266; 90 | 3125.3 | Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H. The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction. Organic letters, 2015, 17, 3256-3259 |
1520656 | CIF | C16 H17 Cl O5 | P -1 | 6.9648; 7.7685; 14.728 76.228; 76.658; 84.002 | 752.04 | Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H. The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction. Organic letters, 2015, 17, 3256-3259 |
1520657 | CIF | C18 H17 Br O5 | P 1 21 1 | 5.6762; 10.5443; 14.1611 90; 100.294; 90 | 833.92 | Sinha, Debarshi; Biswas, Arnab; Singh, Vinod K. Chiral Phosphine-Silver(I) Complex Catalyzed Enantioselective Interrupted Feist-Bénary Reaction with Ynones: The Aldol-Cycloisomerization Cascade. Organic letters, 2015, 17, 3302-3305 |
1520658 | CIF | C19 H20 N2 O6 | P 21 21 21 | 5.8624; 9.6327; 31.868 90; 90; 90 | 1799.61 | Chen, Shi; Ibrahim, Ahmad A.; Mondal, Mukulesh; Magee, Anthony J.; Cruz, Adam J.; Wheeler, Kraig A.; Kerrigan, Nessan J. Asymmetric Synthesis of Deoxypropionate Derivatives via Catalytic Hydrogenolysis of Enantioenriched Z-Ketene Heterodimers. Organic letters, 2015, 17, 3248-3251 |
1520659 | CIF | C22 H32 Cl2 I2 Si2 | P 1 21/n 1 | 13.1915; 9.4009; 22.0383 90; 106.275; 90 | 2623.49 | Sproul, Kyle C.; Chalifoux, Wesley A. Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl. Organic letters, 2015, 17, 3334-3337 |
1520660 | CIF | C16 H10 Cl2 I2 | P b c a | 9.0806; 15.5457; 23.2185 90; 90; 90 | 3277.6 | Sproul, Kyle C.; Chalifoux, Wesley A. Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl. Organic letters, 2015, 17, 3334-3337 |
1520682 | CIF | C26 H19 N3 O5 S | P -1 | 10.4761; 10.8361; 11.3358 76.911; 61.867; 86.563 | 1103.68 | Rao, Wei-Hao; Zhan, Bei-Bei; Chen, Kai; Ling, Peng-Xiang; Zhang, Zhuo-Zhuo; Shi, Bing-Feng Pd(II)-Catalyzed Direct Sulfonylation of Unactivated C(sp(3))-H Bonds with Sodium Sulfinates. Organic letters, 2015, 17, 3552-3555 |
1520683 | CIF | C20 H24 Cl N3 O | P 1 21 1 | 10.868; 6.8325; 12.6102 90; 103.793; 90 | 909.38 | Johnson, Rebecca E.; de Rond, Tristan; Lindsay, Vincent N. G.; Keasling, Jay D.; Sarpong, Richmond Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture. Organic letters, 2015, 17, 3474-3477 |
1520684 | CIF | C13 H17 Cl O3 | P n a 21 | 28.508; 5.4891; 8.1976 90; 90; 90 | 1282.79 | Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S. Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols. Organic letters, 2015, 17, 3482-3485 |
1520685 | CIF | C21 H21 Cl O4 | P b c a | 15.5081; 11.7102; 20.245 90; 90; 90 | 3676.6 | Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S. Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols. Organic letters, 2015, 17, 3482-3485 |
1520686 | CIF | C33 H30 N2 O6 S2 | P -1 | 10.7946; 12.4093; 13.1553 76.627; 68.739; 81.216 | 1593.12 | Yan, Xiaonan; Ling, Fei; Zhang, Yuchen; Ma, Cheng Three-Component Functionalized Dihydropyridine Synthesis via a Formal Inverse Electron-Demand Hetero-Diels-Alder Reaction. Organic letters, 2015, 17, 3536-3539 |
1520694 | CIF | C33 H27 N3 O13 | P -1 | 11.319; 12.665; 14.597 86.284; 86.306; 68.207 | 1937.1 | Chen, Ji-Peng; He, Wei; Yang, Zhen-Yu; Yao, Zhu-Jun Synthesis of Tricyclo[4,3,1,0(1,5)]decane Core of Plumisclerin A Using Pauson-Khand Annulation and SmI2-Mediated Radical Cyclization. Organic letters, 2015, 17, 3379-3381 |
1520702 | CIF | C41 H60 N8 O3 Ti2 | P 1 21/n 1 | 19.8643; 9.0349; 24.8875 90; 106.793; 90 | 4276.1 | Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature. Organic letters, 2015, 17, 3406-3409 |
1520703 | CIF | C163 H221 N28 O13 Ti4 | P -1 | 19.976; 20.518; 21.236 89.583; 78.919; 76.303 | 8292 | Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature. Organic letters, 2015, 17, 3406-3409 |
1520704 | CIF | C22 H20 N2 O3 | P -1 | 11.7148; 11.8534; 14.1205 110; 95.83; 100.677 | 1781.51 | Dörr, Aurélie A; Lubell, William D. γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate. Organic letters, 2015, 17, 3592-3595 |
1520705 | CIF | C22 H22 N2 O3 | P c a 21 | 17.651; 15.5231; 13.7865 90; 90; 90 | 3777.48 | Dörr, Aurélie A; Lubell, William D. γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate. Organic letters, 2015, 17, 3592-3595 |
1520706 | CIF | C22 H20 N2 O3 | P 1 21/n 1 | 15.2406; 5.6664; 20.6863 90; 94.254; 90 | 1781.53 | Dörr, Aurélie A; Lubell, William D. γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate. Organic letters, 2015, 17, 3592-3595 |
1520707 | CIF | C20 H23 N O8 | P 21 21 21 | 8.7215; 11.3257; 19.217 90; 90; 90 | 1898.2 | Paladino, Marco; Zaifman, Joshua; Ciufolini, Marco A. Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol. Organic letters, 2015, 17, 3422-3425 |
1520708 | CIF | C15 H15 N3 O4 | P 1 21/n 1 | 11.4762; 7.95324; 16.5869 90; 107.894; 90 | 1440.7 | Wang, Qi; Tang, Xuli; Luo, Xiangchao; de Voogd, Nicole J.; Li, Pinglin; Li, Guoqiang (+)- and (-)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata. Organic letters, 2015, 17, 3458-3461 |
1520726 | CIF | C44 H42 F6 N6 O7 S2 | P b c a | 21.512; 10.424; 40.881 90; 90; 90 | 9167 | Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids. Organic letters, 2015, 17, 3442-3445 |
1520727 | CIF | C28 H23 F3 N2 O3 | P -1 | 8.882; 10.743; 14.629 87; 76.43; 65.66 | 1234.8 | Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids. Organic letters, 2015, 17, 3442-3445 |
1520728 | CIF | C25 H34 N2 O9 Si | P b c a | 10.3059; 20.6482; 25.5756 90; 90; 90 | 5442.4 | Cheng, Qing-Qing; Qian, Yu; Zavalij, Peter Y.; Doyle, Michael P. Lewis Acid/Rhodium-Catalyzed Formal [3 + 3]-Cycloaddition of Enoldiazoacetates with Donor-Acceptor Cyclopropanes. Organic letters, 2015, 17, 3568-3571 |
1520729 | CIF | C25 H31 N O3 S2 | P 1 21 1 | 6.6067; 19.709; 9.7407 90; 109.22; 90 | 1197.65 | Fernández-Valparís, Javier; Romo, Juan Manuel; Romea, Pedro; Urpí, Fèlix; Kowalski, Hubert; Font-Bardia, Mercè Stereoselective Alkylation of (S)-N-Acyl-4-isopropyl-1,3-thiazolidine-2-thiones Catalyzed by (Me3P)2NiCl2. Organic letters, 2015, 17, 3540-3543 |
1520753 | CIF | C13 H13 Cl N2 O2 S | P 1 21/c 1 | 15.767; 5.759; 15.721 90; 112.32; 90 | 1320.5 | Lu, Lei; Ma, Juan; Qu, Panpan; Li, Feng Effective Recognition of Different Types of Amino Groups: From Aminobenzenesulfonamides to Amino-(N-alkyl)benzenesulfonamides via Iridium-Catalyzed N-Alkylation with Alcohols. Organic letters, 2015, 17, 2350-2353 |
1520754 | CIF | C23 H21 N O3 S2 | P -1 | 7.667; 8.7269; 17.0497 88.1161; 89.15; 62.1966 | 1008.54 | Miura, Tomoya; Funakoshi, Yuuta; Fujimoto, Yoshikazu; Nakahashi, Junki; Murakami, Masahiro Facile synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters. Organic letters, 2015, 17, 2454-2457 |
1520755 | CIF | C270 H372 B6 N8 O30 | C 1 2/c 1 | 52.579; 21.835; 29.598 90; 117.54; 90 | 30130 | Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro Multilayered inclusion nanocycles of anionic spiroborates. Organic letters, 2015, 17, 2466-2469 |
1520756 | CIF | C28 H44 O4 Si2 | P 21 21 21 | 7.702; 13.1321; 27.4999 90; 90; 90 | 2781.4 | Shi, Hang; Tan, Ceheng; Zhang, Weibin; Zhang, Zichun; Long, Rong; Luo, Tuoping; Yang, Zhen Synthetic Progress toward Azadirachtins. 1. Enantio- and Diastereoselective Synthesis of the Left-Wing Fragment of 11-epi-Azadirachtin I. Organic letters, 2015, 17, 2342-2345 |
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