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 |
1520757 | CIF | C24 H20 O3 | P 1 21/c 1 | 17.7328; 8.7774; 13.0228 90; 110.419; 90 | 1899.61 | Li, Mingliang; Yang, Yudong; Zhou, Danni; Wan, Danyang; You, Jingsong Nickel-Catalyzed Addition-Type Alkenylation of Unactivated, Aliphatic C-H Bonds with Alkynes: A Concise Route to Polysubstituted γ-Butyrolactones. Organic letters, 2015, 17, 2546-2549 |
1520758 | CIF | C22 H33 N O9 | P -1 | 9.9044; 11.8847; 11.9608 60.57; 81.21; 75.803 | 1187.9 | Xu, Sanjia; Ciufolini, Marco A. Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone. Organic letters, 2015, 17, 2424-2427 |
1520759 | CIF | C19 H27 N O10 | P -1 | 10.5221; 10.6666; 10.7161 74.105; 73.746; 61.845 | 1003.6 | Xu, Sanjia; Ciufolini, Marco A. Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone. Organic letters, 2015, 17, 2424-2427 |
1520760 | CIF | C22 H36 O3 | P 21 21 21 | 8.1087; 11.9482; 20.232 90; 90; 90 | 1960.2 | Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng Concise synthesis of the core structures of saundersiosides. Organic letters, 2015, 17, 2346-2349 |
1520761 | CIF | C26 H40 O5 | P 21 21 21 | 7.3909; 12.9276; 25.254 90; 90; 90 | 2412.9 | Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng Concise synthesis of the core structures of saundersiosides. Organic letters, 2015, 17, 2346-2349 |
1520762 | CIF | C18 H23 N O4 | P 21 21 21 | 5.2667; 15.2534; 20.3019 90; 90; 90 | 1630.95 | Lin, Cheng-Wei; Hong, Bor-Cherng; Chang, Wan-Chen; Lee, Gene-Hsiang A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis. Organic letters, 2015, 17, 2314-2317 |
1523614 | CIF | C16 H13 N O4 | C 1 2/c 1 | 24.4884; 7.9625; 18.5286 90; 131.954; 90 | 2686.8 | Verma, Akhilesh K.; Danodia, Abhinandan K.; Saunthwal, Rakesh K.; Patel, Monika; Choudhary, Deepak Palladium-Catalyzed Triple Successive C-H Functionalization: Direct Synthesis of Functionalized Carbazoles from Indoles. Organic letters, 2015, 17, 3658-3661 |
1529193 | CIF | C23 H20 Br N O2 | P -1 | 9.823; 10.177; 11.186 92.48; 113.89; 100.8 | 995.5 | Sha, Qiang; Arman, Hadi; Doyle, Michael P. Three-Component Cascade Reactions with 2,3-Diketoesters: A Novel Metal-Free Synthesis of 5-Vinyl-pyrrole and 4-Hydroxy-indole Derivatives. Organic letters, 2015, 17, 3876-3879 |
1529249 | CIF | C13 H18 N2 O4 | P 1 21/n 1 | 9.4119; 7.6136; 18.3824 90; 104.166; 90 | 1277.2 | Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones. Organic letters, 2015, 17, 3860-3863 |
1529250 | CIF | C16 H16 Cl N O2 | P n a 21 | 7.9657; 14.5166; 12.0126 90; 90; 90 | 1389.08 | Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones. Organic letters, 2015, 17, 3860-3863 |
1529257 | CIF | C19 H20 N2 O5 S | P 1 21 1 | 11.1369; 12.7954; 13.7775 90; 105.869; 90 | 1888.49 | Feng, Huan-Xi; Tan, Rui; Liu, Yan-Kai An Efficient One-Pot Approach to the Construction of Chiral Nitrogen-Containing Heterocycles under Mild Conditions. Organic letters, 2015, 17, 3794-3797 |
1529280 | CIF | C17 H13 N | P 1 21/c 1 | 8.8383; 21.101; 6.6024 90; 91.311; 90 | 1231 | Mandal, Sumana; Mahato, Sujit; Jana, Chandan K. Direct β-C(sp(3))-H Functionalization of Aliphatic Amines to α,β-Unsaturated Imines, Aldehydes, and Chromenes. Organic letters, 2015, 17, 3762-3765 |
1529281 | CIF | C24 H21 N O4 S | P 1 21/c 1 | 17.7457; 5.8725; 20.1502 90; 103.189; 90 | 2044.5 | Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones. Organic letters, 2015, 17, 3846-3849 |
1529282 | CIF | C17 H13 Br O2 | P n a 21 | 29.2958; 6.1415; 15.5413 90; 90; 90 | 2796.2 | Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones. Organic letters, 2015, 17, 3846-3849 |
1529283 | CIF | C18 H27 N O4 | P 21 21 21 | 10.1466; 10.1835; 16.6612 90; 90; 90 | 1721.57 | Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone. Organic letters, 2015, 17, 3938-3940 |
1529284 | CIF | C17 H27 N O2 | P 1 21 1 | 8.2578; 7.6701; 12.4589 90; 99.389; 90 | 778.55 | Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone. Organic letters, 2015, 17, 3938-3940 |
1529285 | CIF | C18 H25 N O4 | P 1 21 1 | 8.5383; 7.6057; 12.8523 90; 104.589; 90 | 807.71 | Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone. Organic letters, 2015, 17, 3938-3940 |
1529293 | CIF | C21 H22 N2 O2 | P 21 21 21 | 8.8494; 10.974; 17.557 90; 90; 90 | 1705 | Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy. Organic letters, 2015, 17, 3918-3921 |
1529294 | CIF | C22 H20 N2 O | P -1 | 10.3796; 12.9633; 14.3864 71.474; 71.763; 68.137 | 1661.2 | Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy. Organic letters, 2015, 17, 3918-3921 |
1529307 | CIF | C29 H36 O7 Si | P 1 21/c 1 | 14.1631; 11.4869; 16.4977 90; 94.808; 90 | 2674.57 | Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle. Organic letters, 2015, 17, 3746-3749 |
1529349 | CIF | C36 H62 Cl2 Cu2 O6 P2 S2 | P 1 21 1 | 10.6416; 13.3076; 17.3445 90; 92.328; 90 | 2454.2 | Wang, Ding; Cao, Peng; Wang, Bing; Jia, Tao; Lou, Yazhou; Wang, Min; Liao, Jian Copper(I)-Catalyzed Asymmetric Pinacolboryl Addition of N-Boc-imines Using a Chiral Sulfoxide-Phosphine Ligand. Organic letters, 2015, 17, 2420-2423 |
1529350 | CIF | C16 H10 Br F3 N2 O2 S | I 1 2/a 1 | 11.4371; 13.3473; 22.4306 90; 101.301; 90 | 3357.74 | Lee, Eunsook; Ryu, Taekyu; Shin, Eunji; Son, Jeong-Yu; Choi, Wonseok; Lee, Phil Ho Synthesis of 2-bromoimidazoles from alkynes, N-sulfonylazides, and bromocyanides. Organic letters, 2015, 17, 2470-2473 |
1529362 | CIF | C32 H22 N6 | P 1 21/c 1 | 15.6612; 9.6881; 16.3377 90; 96.112; 90 | 2464.8 | Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A. Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States. Organic letters, 2015, 17, 4026-4029 |
1529363 | CIF | C34 H26 Cl2 N6 | P -1 | 8.8511; 9.8863; 16.5742 107.267; 92.876; 90.368 | 1382.87 | Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A. Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States. Organic letters, 2015, 17, 4026-4029 |
1529370 | CIF | C22 H18 F3 N O4 S | P 1 21/c 1 | 15.9; 21.601; 19.802 90; 110.332; 90 | 6377.4 | Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Organic letters, 2015, 17, 3944-3947 |
1529371 | CIF | C28 H24 F3 N O5 S | P -1 | 12.978; 13.576; 16.636 84.126; 79.909; 65.828 | 2631.2 | Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Organic letters, 2015, 17, 3944-3947 |
1529372 | CIF | C28 H24 F3 N O4 S | P 1 21/n 1 | 15.6589; 9.9834; 16.2519 90; 92.274; 90 | 2538.6 | Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Organic letters, 2015, 17, 3944-3947 |
1529373 | CIF | C24 H24 F3 N O4 S | P -1 | 10.562; 11.1083; 11.2554 85.47; 66.868; 84.789 | 1208 | Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Organic letters, 2015, 17, 3944-3947 |
1529374 | CIF | C22 H20 N2 O2 S | P 1 21/c 1 | 11.5958; 12.0999; 14.031 90; 97.891; 90 | 1950 | Zeng, Ting-Ting; Xuan, Jun; Ding, Wei; Wang, Kuan; Lu, Liang-Qiu; Xiao, Wen-Jing [3 + 2] Cycloaddition/Oxidative Aromatization Sequence via Photoredox Catalysis: One-Pot Synthesis of Oxazoles from 2H-Azirines and Aldehydes. Organic letters, 2015, 17, 4070-4073 |
1529381 | CIF | C114 H172 Cl K Li0 N47 O38 | C 1 2/c 1 | 29.3719; 14.1615; 33.703 90; 101.172; 90 | 13753.1 | Lu, Xiaoyong; Isaacs, Lyle Synthesis and Recognition Properties of Enantiomerically Pure Acyclic Cucurbit[n]uril-Type Molecular Containers. Organic letters, 2015, 17, 4038-4041 |
1529393 | CIF | C25 H24 Cl N O5 | P 21 21 21 | 6.9051; 18.0332; 18.2794 90; 90; 90 | 2276.2 | Liu, Qiong-Jie; Yan, Wen-Guang; Wang, Lijia; Zhang, X. Peter; Tang, Yong One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles. Organic letters, 2015, 17, 4014-4017 |
1529398 | CIF | C25 H23 N O6 | C 1 2/c 1 | 31.5153; 8.7548; 18.0436 90; 123.435; 90 | 4154.5 | Huang, Jing-Kai; Yang Lauderdale, Tsai-Ling; Shia, Kak-Shan Studies on Antibiotics Active against Resistant Bacteria. Total Synthesis of MRSA-Active Tetarimycin A and Its Analogues. Organic letters, 2015, 17, 4248-4251 |
1529399 | CIF | C55 H35 B F2 N2 | P 1 21/c 1 | 16.4511; 17.491; 13.5624 90; 98.856; 90 | 3856 | Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction. Organic letters, 2015, 17, 4168-4171 |
1529400 | CIF | C55 H36 B F7 N2 | P 1 21/c 1 | 13.1321; 10.7218; 30.2961 90; 96.85; 90 | 4235.23 | Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction. Organic letters, 2015, 17, 4168-4171 |
1529401 | CIF | C55 H41 B F2 N2 | C 1 2/c 1 | 21.491; 13.7296; 29.3488 90; 106.144; 90 | 8318.3 | Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction. Organic letters, 2015, 17, 4168-4171 |
1529402 | CIF | C19 H20 Br N O | P 1 21 1 | 5.225; 13.44; 11.8487 90; 90.133; 90 | 832.06 | Dziechciejewski, Wojciech J.; Weber, Regina; Sowada, Oliver; Boysen, Mike M. K. Cycloalkene Carbonitriles in Rhodium-Catalyzed 1,4-Addition and Formal Synthesis of Vabicaserin. Organic letters, 2015, 17, 4132-4135 |
1529420 | CIF | C21 H23 Cl F2 N2 O | C 1 c 1 | 13.1195; 25.1207; 6.0786 90; 103.299; 90 | 1949.6 | Chen, Qiao; Zhou, Jiawei; Wang, Yanan; Wang, Chao; Liu, Xihong; Xu, Zhaoqing; Lin, Li; Wang, Rui Transition-Metal-Free Dehydrosilylative Difluoroamidation of Tetrahydroisoquinolines under Mild Conditions. Organic letters, 2015, 17, 4212-4215 |
1529421 | CIF | C13 H18 O4 | P 1 21 1 | 5.917; 7.864; 13.651 90; 101.24; 90 | 623 | Rybak, Taras; Hall, Dennis G. Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B. Organic letters, 2015, 17, 4156-4159 |
1529422 | CIF | C13 H18 O3 | P 1 21/n 1 | 9.7101; 10.6909; 23.0359 90; 92.6548; 90 | 2388.78 | Rybak, Taras; Hall, Dennis G. Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B. Organic letters, 2015, 17, 4156-4159 |
1529423 | CIF | C42 H33 Cl2 Ir N2 O5 | P 1 21/n 1 | 18.021; 10.891; 18.559 90; 103.69; 90 | 3539 | Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone. Organic letters, 2015, 17, 4204-4207 |
1529424 | CIF | C28 H18 Cl2 N2 O5 | P -1 | 10.069; 10.87; 12.021 71.67; 82.11; 82.87 | 1232.5 | Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone. Organic letters, 2015, 17, 4204-4207 |
1529448 | CIF | C15 H18 Cl N O2 | P -1 | 11.1941; 11.9877; 12.3151 117.921; 101.02; 90.422 | 1424.3 | Deng, Yongming; Jing, Changcheng; Zavalij, Peter Y.; Doyle, Michael P. Hg(OTf)2 Catalyzed Intramolecular 1,4-Addition of Donor-Acceptor Cyclopropenes to Arenes. Organic letters, 2015, 17, 4312-4315 |
1529469 | CIF | C22 H35 N O3 | P 21 21 21 | 6.212; 12.231; 28.133 90; 90; 90 | 2137.5 | Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp. Organic letters, 2015, 17, 4304-4307 |
1529470 | CIF | C22 H33 N O3.5 | P 21 21 21 | 12.515; 14.907; 45.898 90; 90; 90 | 8563 | Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp. Organic letters, 2015, 17, 4304-4307 |
1529473 | CIF | C28 H29 N5 O4 | P -1 | 7.7823; 10.8987; 15.2414 72.781; 83.016; 85.094 | 1224 | Samanta, Ritwik; Kumar, B. Sathish; Panda, Pradeepta K. Calix[4]pyrroles with Shortest Possible Strap: Exclusively Selective toward Fluoride Ion. Organic letters, 2015, 17, 4140-4143 |
1529503 | CIF | C25 H22 Cl3 F3 N2 O2 S | P -1 | 8.374; 10.228; 16.064 99.954; 98.372; 101.416 | 1305.1 | Wei, Qiang; Chen, Jia-Rong; Hu, Xiao-Qiang; Yang, Xiao-Chen; Lu, Bin; Xiao, Wen-Jing Photocatalytic Radical Trifluoromethylation/Cyclization Cascade: Synthesis of CF3-Containing Pyrazolines and Isoxazolines. Organic letters, 2015, 17, 4464-4467 |
1529847 | CIF | C21 H22 N2 O2 | P 1 21 1 | 9.702; 7.4213; 12.862 90; 103.265; 90 | 901.4 | Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy. Organic letters, 2015, 17, 3918-3921 |
1529848 | CIF | C17 H20 O6 | P 1 21/c 1 | 13.5566; 9.9192; 12.1878 90; 114.983; 90 | 1485.55 | Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle. Organic letters, 2015, 17, 3746-3749 |
1529849 | CIF | C37 H54 O6 Si | P 1 21/c 1 | 9.8958; 32.0974; 20.6189 90; 92.873; 90 | 6540.9 | Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle. Organic letters, 2015, 17, 3746-3749 |
1529850 | CIF | C16 H12 Br F2 N3 | P 1 21/c 1 | 15.027; 8.8571; 11.123 90; 96.542; 90 | 1470.8 | Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio Difluoromethylation of Terminal Alkynes by Fluoroform. Organic letters, 2015, 17, 3802-3805 |
1529851 | CIF | C16 H10 Br F2 N O | P 1 21/n 1 | 17.957; 6.8848; 22.81 90; 99.781; 90 | 2779 | Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio Difluoromethylation of Terminal Alkynes by Fluoroform. Organic letters, 2015, 17, 3802-3805 |
1529852 | CIF | C43 H37 Br2 Cl Cu N3 O4 P2 | P n a 21 | 19.3661; 14.8237; 28.5913 90; 90; 90 | 8207.9 | Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst. Organic letters, 2015, 17, 3814-3817 |
1529853 | CIF | C17 H19 N O3 | P -1 | 5.7487; 9.5873; 13.7161 85.932; 86.522; 90.042 | 752.65 | Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst. Organic letters, 2015, 17, 3814-3817 |
1529854 | CIF | C18 H16 Br N O3 S | P 21 21 21 | 7.9153; 11.4655; 18.152 90; 90; 90 | 1647.3 | Xiao, Yonglong; Wang, Jinxin; Xia, Wenjing; Shu, Shuangjie; Jiao, Shenchao; Zhou, Yu; Liu, Hong γ-Carbon Activation through N-Heterocyclic Carbene/Brønsted Acids Cooperative Catalysis: A Highly Enantioselective Route to δ-Lactams. Organic letters, 2015, 17, 3850-3853 |
1529855 | CIF | C26 H18 N2 O S | P 1 21/n 1 | 9.919; 19.032; 11.221 90; 102.942; 90 | 2064.5 | Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones. Organic letters, 2015, 17, 3872-3875 |
1529856 | CIF | C29 H21 Br N2 O | P -1 | 9.724; 11.142; 12.91 98.826; 103.604; 112.844 | 1205.2 | Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones. Organic letters, 2015, 17, 3872-3875 |
1529857 | CIF | C20 H22 N2 O5 S | P 21 21 21 | 6.8305; 13.7709; 21.5589 90; 90; 90 | 2027.88 | Rao, Wei-Hao; Yin, Xue-Song; Shi, Bing-Feng Catalyst-Controlled Amino- versus Oxy-Acetoxylation of Urea-Tethered Alkenes: Efficient Synthesis of Cyclic Ureas and Isoureas. Organic letters, 2015, 17, 3758-3761 |
1529858 | CIF | C20 H22 N2 O5 S | P -1 | 5.9849; 8.35; 21.2894 90.789; 92.849; 107.436 | 1013.32 | Rao, Wei-Hao; Yin, Xue-Song; Shi, Bing-Feng Catalyst-Controlled Amino- versus Oxy-Acetoxylation of Urea-Tethered Alkenes: Efficient Synthesis of Cyclic Ureas and Isoureas. Organic letters, 2015, 17, 3758-3761 |
1529859 | CIF | C24 H17 Br F3 N O4 | P 32 2 1 | 12.075; 12.075; 26.601 90; 90; 120 | 3358.9 | Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes. Organic letters, 2015, 17, 3826-3829 |
1529860 | CIF | C18 H13 Cl F3 N O4 | P 21 21 21 | 10.916; 12.171; 27.176 90; 90; 90 | 3610.6 | Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes. Organic letters, 2015, 17, 3826-3829 |
1529861 | CIF | C19 H15 Br F3 N O4 | P 21 21 21 | 8.3159; 9.4678; 23.6499 90; 90; 90 | 1862 | Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes. Organic letters, 2015, 17, 3826-3829 |
1529862 | CIF | C25 H22 F N3 O3 | P 1 21/n 1 | 11.943; 12.618; 14.512 90; 90.2; 90 | 2186.9 | Miao, Jinmin; Yang, Ke; Kurek, Martin; Ge, Haibo Palladium-Catalyzed Site-Selective Fluorination of Unactivated C(sp(3))-H Bonds. Organic letters, 2015, 17, 3738-3741 |
1529863 | CIF | C25 H26 O2 | P b c a | 12.3364; 8.7782; 36.9717 90; 90; 90 | 4003.7 | Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L. Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J. Organic letters, 2015, 17, 3884-3887 |
1529864 | CIF | C32 H30 O2 | P -1 | 7.0588; 11.869; 15.6316 105.145; 101.933; 100.657 | 1196.58 | Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L. Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J. Organic letters, 2015, 17, 3884-3887 |
1529865 | CIF | C35 H36 O5 | P 1 21/c 1 | 14.7165; 5.7937; 33.4045 90; 101.755; 90 | 2788.43 | Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L. Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J. Organic letters, 2015, 17, 3884-3887 |
1529866 | CIF | C24 H23 N O3 S | P -1 | 9.2832; 10.302; 12.39 76.387; 83.994; 64.267 | 1037.4 | Zhang, Xiaojuan; Han, Xiuling; Lu, Xiyan Cationic Pd(II)-Catalyzed Cyclization of N-Tosyl-aniline Tethered Allenyl Aldehydes with Arylboronic Acids: Diastereo- and Enantioselective Synthesis of Tetrahydroquinoline Derivatives. Organic letters, 2015, 17, 3910-3913 |
1529867 | CIF | C66 H60 Cl9 N6 O6 P3 | R -3 :H | 17.622; 17.622; 37.634 90; 90; 120 | 10121 | Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution. Organic letters, 2015, 17, 3650-3653 |
1529868 | CIF | C67 H65 N6 O8 P3 | P -1 | 13.721; 14.84; 15.073 94.518; 91.104; 100.582 | 3006 | Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution. Organic letters, 2015, 17, 3650-3653 |
1529869 | CIF | C67 H63 N8 O6 P3 | P -1 | 13.731; 14.962; 15.117 94.572; 91.24; 101.538 | 3031 | Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution. Organic letters, 2015, 17, 3650-3653 |
1529870 | CIF | C66 H65 N6 O7 P3 | P -1 | 12.58; 13.197; 19.419 80.816; 80.935; 69.837 | 2969.2 | Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution. Organic letters, 2015, 17, 3650-3653 |
1529871 | CIF | C63 H57 N6 O9 P3 | P 31 | 13.914; 13.914; 28.339 90; 90; 120 | 4751.4 | Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution. Organic letters, 2015, 17, 3650-3653 |
1529872 | CIF | C65 H63 N6 O7 P3 S | P -1 | 13.123; 13.188; 19.257 73.751; 79.26; 66.588 | 2925.5 | Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution. Organic letters, 2015, 17, 3650-3653 |
1529873 | CIF | C20 H24 N2 O4 | P 1 21 1 | 11.5233; 7.6374; 11.6452 90; 110.244; 90 | 961.56 | Reddy, B. V. Subba; Reddy, C. Ravikumar; Reddy, M. Rajashekhar; Yarlagadda, Suresh; Sridhar, B. Substrate Directed C-H Activation for the Synthesis of Benzo[c]cinnolines through a Sequential C-C and C-N Bond Formation. Organic letters, 2015, 17, 3730-3733 |
1529874 | CIF | C20 H18 O7 | P 21 21 21 | 5.968; 10.51; 25.663 90; 90; 90 | 1609.7 | Zhao, Ming; Onakpa, Monday M.; Santarsiero, Bernard D.; Huang, Xiao-Jun; Zhang, Xiao-Qi; Chen, Jia; Cheng, Jian-Jun; Longnecker, Richard; Che, Chun-Tao Icacinlactone H and Icacintrichantholide from the Tuber of Icacina trichantha. Organic letters, 2015, 17, 3834-3837 |
1529875 | CIF | C20 H20 O7 | P 21 21 2 | 6.8018; 20.5957; 12.4023 90; 90; 90 | 1737.41 | Zhao, Ming; Onakpa, Monday M.; Santarsiero, Bernard D.; Huang, Xiao-Jun; Zhang, Xiao-Qi; Chen, Jia; Cheng, Jian-Jun; Longnecker, Richard; Che, Chun-Tao Icacinlactone H and Icacintrichantholide from the Tuber of Icacina trichantha. Organic letters, 2015, 17, 3834-3837 |
1529876 | CIF | C23 H27 F3 O7 S | P -1 | 9.578; 10.805; 12.575 102.754; 97.366; 93.699 | 1253 | Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes. Organic letters, 2015, 17, 3694-3697 |
1529877 | CIF | C22 H21 Cl F3 N O2 S2 | P 1 21/c 1 | 5.4961; 23.714; 17.6522 90; 96.871; 90 | 2284.2 | Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes. Organic letters, 2015, 17, 3694-3697 |
1529878 | CIF | C16 H15 F3 O3 S | P 1 21/c 1 | 9.9242; 15.9342; 10.0614 90; 106.109; 90 | 1528.58 | Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes. Organic letters, 2015, 17, 3694-3697 |
1529879 | CIF | C14 H12 Br N O | P 1 21/c 1 | 6.1858; 17.934; 11.7423 90; 101.212; 90 | 1277.8 | Haidzinskaya, Tatsiana; Kerchner, Hilary A.; Liu, Jixin; Watson, Mary P. Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions. Organic letters, 2015, 17, 3857-3859 |
1529880 | CIF | C12 H13 Br O3 | P 1 21/c 1 | 5.7983; 8.1321; 24.8527 90; 90.153; 90 | 1171.86 | Haidzinskaya, Tatsiana; Kerchner, Hilary A.; Liu, Jixin; Watson, Mary P. Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions. Organic letters, 2015, 17, 3857-3859 |
1529881 | CIF | C14 H15 N3 O2 | P 1 21/n 1 | 6.6041; 7.3454; 25.445 90; 90.254; 90 | 1234.3 | Komkov, Alexander V.; Komendantova, Anna S.; Menchikov, Leonid G.; Chernoburova, Elena I.; Volkova, Yulia A.; Zavarzin, Igor V. A Straightforward Approach toward Multifunctionalized Pyridazines via Imination/Electrocyclization. Organic letters, 2015, 17, 3734-3737 |
1529882 | CIF | C27 H19 F3 N2 | P 1 21/c 1 | 7.4962; 17.6328; 16.4671 90; 93.865; 90 | 2171.65 | Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds. Organic letters, 2015, 17, 3790-3793 |
1529883 | CIF | C19 H17 N O2 | P 21 21 21 | 7.3862; 11.9598; 17.2782 90; 90; 90 | 1526.31 | Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds. Organic letters, 2015, 17, 3790-3793 |
1529884 | CIF | C26 H20 N2 | C 1 2/c 1 | 21.3348; 10.673; 18.3612 90; 110.777; 90 | 3909.1 | Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds. Organic letters, 2015, 17, 3790-3793 |
1529885 | CIF | C32 H22 N6 | P 1 21/c 1 | 13.4407; 21.762; 8.4346 90; 99.174; 90 | 2435.5 | Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A. Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States. Organic letters, 2015, 17, 4026-4029 |
1529886 | CIF | C28 H24 F3 N O4 S | P -1 | 10.2147; 11.39; 12.1881 68.285; 71.067; 83.51 | 1246.1 | Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Organic letters, 2015, 17, 3944-3947 |
1530387 | CIF | C32 H59 N O4 Si2 | P 1 21 1 | 16.472; 18.563; 11.996 90; 92.581; 90 | 3664.3 | Fanelli, Roberto; Salah, Khoubaib Ben Haj; Inguimbert, Nicolas; Didierjean, Claude; Martinez, Jean; Cavelier, Florine Access to α,α-Disubstituted Disilylated Amino Acids and Their Use in Solid-Phase Peptide Synthesis. Organic letters, 2015, 17, 4498-4501 |
1530388 | CIF | C22 H22 N2 O3 S | P 1 21/n 1 | 13.4257; 10.9838; 14.5635 90; 109.954; 90 | 2018.7 | Wang, Chen; Zhang, Haojie; Lang, Bo; Ren, Anni; Lu, Ping; Wang, Yanguang Rh-Catalyzed Reactions of 3-Diazoindolin-2-imines: Synthesis of Pyridoindoles and Tetrahydrofuropyrroloindoles. Organic letters, 2015, 17, 4412-4415 |
1530389 | CIF | C17 H16 N2 O | P 1 21/n 1 | 7.6543; 11.1582; 16.8881 90; 101.198; 90 | 1414.9 | Wang, Chen; Zhang, Haojie; Lang, Bo; Ren, Anni; Lu, Ping; Wang, Yanguang Rh-Catalyzed Reactions of 3-Diazoindolin-2-imines: Synthesis of Pyridoindoles and Tetrahydrofuropyrroloindoles. Organic letters, 2015, 17, 4412-4415 |
1530390 | CIF | C29 H44 O4 | P 21 21 21 | 7.3491; 11.3041; 30.6417 90; 90; 90 | 2545.56 | Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea. Organic letters, 2015, 17, 4616-4619 |
1530391 | CIF | C32 H48 O5 | P 1 21 1 | 7.3331; 10.1624; 19.3573 90; 97.23; 90 | 1431.07 | Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea. Organic letters, 2015, 17, 4616-4619 |
1530392 | CIF | C29 H44 O4 | P 1 | 7.357; 11.5004; 15.8083 101.789; 102.383; 90.228 | 1277.24 | Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea. Organic letters, 2015, 17, 4616-4619 |
1530393 | CIF | C34 H54 O6 | P 1 21 1 | 7.9562; 33.6801; 12.617 90; 107.429; 90 | 3225.7 | Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea. Organic letters, 2015, 17, 4616-4619 |
1531034 | CIF | C23 H22 N2 O5 | P 1 21/c 1 | 10.82123; 22.8438; 8.59627 90; 108.437; 90 | 2015.91 | Zhan, Gu; Shi, Ming-Lin; He, Qing; Du, Wei; Chen, Ying-Chun [4 + 3] Cycloadditions with Bromo-Substituted Morita-Baylis-Hillman Adducts of Isatins and N-(ortho-Chloromethyl)aryl Amides. Organic letters, 2015, 17, 4750-4753 |
1531035 | CIF | C93 H37 Cu F35 N14 | P -1 | 16.017; 18.231; 18.359 115.519; 101.669; 92.884 | 4680.3 | Zhang, Kai; Zhang, Junda; Li, Xin; Guo, Rui; Ågren, Hans; Ou, Zhongping; Ishida, Masatoshi; Furuta, Hiroyuki; Xie, Yongshu Synthesis of a Neo-Confused Octaphyrin and the Formation of Its Mononuclear Complexes. Organic letters, 2015, 17, 4806-4809 |
1531036 | CIF | C89 H31 F35 N12 Zn | P -1 | 16.045; 18.292; 18.495 115.633; 101.728; 93.013 | 4730.7 | Zhang, Kai; Zhang, Junda; Li, Xin; Guo, Rui; Ågren, Hans; Ou, Zhongping; Ishida, Masatoshi; Furuta, Hiroyuki; Xie, Yongshu Synthesis of a Neo-Confused Octaphyrin and the Formation of Its Mononuclear Complexes. Organic letters, 2015, 17, 4806-4809 |
1531166 | CIF | C28 H26 N2 O4 S2 | P -1 | 9.2332; 11.8033; 13.4383 78.564; 74.091; 80.538 | 1371.04 | Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines. Organic letters, 2015, 17, 4870-4873 |
1531170 | CIF | C28 H26 N2 O4 S2 | P 21 21 21 | 7.8395; 12.02537; 26.9644 90; 90; 90 | 2542.01 | Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines. Organic letters, 2015, 17, 4870-4873 |
1531174 | CIF | C28 H26 N2 O4 S2 | P 21 21 21 | 5.35547; 17.35361; 27.184 90; 90; 90 | 2526.39 | Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines. Organic letters, 2015, 17, 4870-4873 |
1532457 | CIF | C32 H40 S3 | P -1 | 9.799; 11.932; 13.735 84.22; 72.85; 66.98 | 1412.1 | Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji Synthesis and Properties of Ethene-Bridged Terthiophenes. Organic letters, 2015, 17, 4858-4861 |
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