Crystallography Open Database

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1520309 CIFC12 H18 B F2 N O3P 1 21 114.7772; 11.1085; 16.6848
90; 92.405; 90
2736.4Roßbach, 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 CIFC13 H20 B F2 N O3P 1 21/n 110.6399; 11.8723; 11.9174
90; 107.028; 90
1439.41Roßbach, 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 CIFC12 H18 B F2 N O4P -111.3963; 11.7254; 12.5468
74.986; 64.116; 64.237
1353.47Roßbach, 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 CIFC10 H16 B F2 N O4I b a 212.1721; 49.556; 8.341
90; 90; 90
5031.3Roßbach, 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 CIFC10 H16 B F2 N O4P -17.0022; 7.7079; 12.3657
83.232; 83.476; 76.265
641.26Roßbach, 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 CIFC10 H17 N O4P -17.8792; 8.1476; 10.2749
106.191; 106.585; 104.538
566.58Roßbach, 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 CIFC12 H20 B F2 N O4P b c a16.8311; 9.1985; 18.0999
90; 90; 90
2802.24Roßbach, 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 CIFC12 H18 B Br2 F2 N O4P 1 21/c 110.3517; 15.7916; 9.5485
90; 99.476; 90
1539.59Roßbach, 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 CIFC8 H11 Br O4P 1 21/c 18.8688; 18.0772; 6.0396
90; 94.753; 90
964.96Roßbach, 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 CIFC19 H23.6 B F2 N2 O5.3P b c n12.2584; 10.1061; 31.0115
90; 90; 90
3841.8Roßbach, 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 CIFC19 H23 B F2 N2 O5P 1 21/n 115.4609; 8.0727; 15.6576
90; 103.611; 90
1899.36Roßbach, 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 CIFC30 H25 N2 O4 PP 1 21/c 112.5638; 14.8917; 13.7164
90; 104.477; 90
2484.8Yamamura, 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 CIFC41 H45 Cl2 N5 O18P -118.718; 20.1801; 21.555
63.466; 65.8; 82.646
6629.1Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520386 CIFC48 H53 N5 O16 S2P 1 21/n 19.5948; 11.7166; 43.6295
90; 91.392; 90
4903.3Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520387 CIFC48 H51 N5 O13 SP 1 21/c 110.656; 38.925; 11.435
90; 111.21; 90
4422Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520388 CIFC22 H19 N O2P 21 21 218.6008; 10.6881; 18.1
90; 90; 90
1663.9Battini, 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 CIFC26 H18 B Cl2 F8 N3P 1 21/c 17.923; 11.039; 27.77
90; 96.981; 90
2410.8Maeda, 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 CIFC26.14 H22.79 B Cl0.79 F2 N3 O3.24P 1 21/c 113.159; 12.065; 15.082
90; 98.075; 90
2370.7Maeda, 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 CIFC707 H656 B16 F32 N48 O9P 1 21/c 115.429; 41.602; 24.49
90; 91.209; 90
15716Maeda, 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 CIFC35.79 H27.57 B Cl1.57 F2 N3C 1 2/c 133.021; 10.588; 23.034
90; 132.89; 90
5900Maeda, 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 CIFC32 H24 B Cl2 F2 N3P -17.3425; 11.0127; 15.884
94.772; 97.467; 91.375
1268.3Maeda, 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 CIFC50.45 H44.9 B Cl2.9 F2 N3P 1 21/c 18.0911; 21.853; 25.007
90; 97.291; 90
4385.9Maeda, 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 CIFC23 H18 B F2 N3P 1 21/n 19.594; 8.7428; 21.526
90; 100.795; 90
1773.6Maeda, 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 CIFC16 H15 N O2 S2P c a 2118.773; 7.8448; 20.3148
90; 90; 90
2991.8Siva 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 CIFC16 H14 F N O2 S2P 1 21/c 115.7817; 13.0488; 7.2719
90; 92.391; 90
1496.2Siva 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 CIFC16 H15 N O3 S2P -19.7686; 10.4236; 16.0412
90.974; 91.846; 107.681
1554.8Siva 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 CIFC16 H15 N O2 S SeP b c a7.38023; 12.875; 31.8273
90; 90; 90
3024.24Siva 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 CIFC17 H17 N O2 S2P 1 21/n 16.63588; 12.9255; 19.0476
90; 93.665; 90
1630.41Siva 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 CIFC40 H32 N2P 1 21/n 112.149; 7.34; 16.53
90; 101.456; 90
1444.7Xu, 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 CIFC60 H74 N4 O4P -111.2497; 12.373; 20.0241
95.185; 106.067; 94.622
2651.1Xia, 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 CIFC20 H16 I N OP -110.699; 11.726; 22.2683
94.284; 101.795; 109.369
2549Wang, 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 CIFC20 H16 I N OP b c a7.2355; 20.9295; 23.0167
90; 90; 90
3485.5Wang, 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 CIFC24 H24P 1 21/n 17.4014; 30.606; 7.739
90; 100.806; 90
1722Chang, 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 CIFC20 H24 O4 SP 1 n 111.2988; 5.7063; 14.045
90; 102.129; 90
885.3Chang, 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 CIFC25 H29 N O5 SF d d 222.419; 52.094; 7.523
90; 90; 90
8786Chang, 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 CIFC25 H29 N O5 SC 1 2/c 130.166; 11.6914; 14.2065
90; 113.297; 90
4601.9Chang, 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 CIFC19 H19 F OP 21 21 218.4903; 9.6656; 18.663
90; 90; 90
1531.6Chang, 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 CIFC43 H41 N3 O4P 1 21/c 131.617; 15.428; 14.478
90; 101.899; 90
6910Zhang, Feng-Lian; Zhu, Xu; Chiba, Shunsuke
Tf~2~NH-Catalyzed Amide Synthesis from Vinyl Azides and Alcohols
Organic Letters, 2015, 17, 3138-3141
1520519 CIFC13 H12 Cl N O4P 21 21 217.9023; 12.49; 12.9
90; 90; 90
1273.2Sekikawa, 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 CIFC39 H40 B F2 N3 O4P -18.745; 10.225; 20.19
89.48; 86.38; 65.669
1641.4Hiruta, 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 CIFC37.5 H36.5 B Cl1.5 F2 N3 O4P -18.776; 10.567; 19.225
84.193; 82.204; 69.585
1652.6Hiruta, 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 CIFC46 H44 B2 N2 O2P 1 21/c 17.274; 17.864; 15.322
90; 100.332; 90
1958.7Kubota, 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 CIFC42 H36 B2 N2 O2P 1 21/c 17.054; 17.672; 13.751
90; 96.406; 90
1703.5Kubota, 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 CIFC32 H25 N O4P 1 21 16.62144; 20.1343; 9.362
90; 100.915; 90
1225.54Zhao, 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 CIFC25 H24 SP -19.4128; 9.6074; 12.0794
97.999; 97.992; 108.357
1007.08Zhang, 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 CIFC36 H22 N12P 1 21/n 115.3809; 11.5149; 17.7975
90; 90.677; 90
3151.9Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520553 CIFC35 H19 F4 N6 O2 PI b a 221.689; 29.869; 10.7143
90; 90; 90
6941Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520554 CIFC51 H33 Co F4 N8P 1 21/c 112.3996; 15.4999; 21.5037
90; 97.248; 90
4099.8Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520555 CIFC24 H20 Br2 N2C 1 2/c 116.3504; 14.9527; 9.2389
90; 92.387; 90
2256.8Laird, 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 CIFC24 H18 N2P -19.4274; 12.3411; 15.5934
83.302; 82.714; 79.24
1759.9Laird, 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 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.33; 10.8862; 17.8919
90; 110.048; 90
2622Laird, 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 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.3809; 10.9748; 11.0438
109.43; 98.185; 97.328
1153.7Laird, 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 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.4495; 11.0503; 11.0576
109.671; 96.586; 97.962
1172.8Laird, 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 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.369; 10.925; 18.106
90; 110.574; 90
2661Laird, 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 CIFC51 H58 F6 O14 S2P -111.2709; 11.7647; 20.1194
88.271; 83.035; 86.352
2642.1Han, 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 CIFC46 H46 Cl2 F6 O14 S2P 1 n 111.616; 18.2419; 11.617
90; 94.1589; 90
2455.14Han, 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 CIFC48.75 H55.04 Cl2.25 F3 O12 SP n a 2135.9931; 12.0648; 11.369
90; 90; 90
4937Han, 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 CIFC51 H58 F6 O14 S2P 21 21 2111.3045; 12.1357; 37.187
90; 90; 90
5101.6Han, 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 CIFC51 H55 F9 O16 S3P 1 21/c 122.0373; 11.9982; 22.7155
90; 110.288; 90
5633.5Han, 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 CIFC51 H55 F9 O16 S3P b c a20.6289; 22.2856; 24.1696
90; 90; 90
11111.4Han, 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 CIFC17 H15 N SP 21 21 216.1669; 12.182; 17.8605
90; 90; 90
1341.77Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520574 CIFC19 H17 N OP b c a7.4565; 18.3137; 20.6855
90; 90; 90
2824.73Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520575 CIFC16 H15 N3P 1 21/m 19.7773; 6.90436; 9.79548
90; 98.985; 90
653.14Castillo, 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 CIFC21 H15 N3P 1 21/c 114.0946; 11.4421; 9.74761
90; 99.2056; 90
1551.77Castillo, 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 CIFC20 H20 O6P 21 21 2110.1756; 12.2477; 13.4918
90; 90; 90
1681.45Bautista, 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 CIFC25 H23 N O3P 1 21/c 19.4141; 23.293; 9.0609
90; 92.942; 90
1984.3Brady, 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 CIFC18 H17 N O2P 1 21/c 18.0166; 15.8594; 11.2674
90; 98.788; 90
1415.7Brady, 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 CIFC37 H31 N O5P 1 21/n 111.364; 10.93; 24.447
90; 96.564; 90
3017Mo, 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 CIFC22 H21 Br N2 O3 S2P b c a11.7745; 15.3391; 24.3582
90; 90; 90
4399.34Choi, 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 CIFC22 H20 N2 O4 S2P -19.0038; 10.66; 11.8108
75.2664; 76.0323; 75.5364
1042.26Choi, 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 CIFC30 H29 N O3P 21 21 217.37176; 14.7771; 21.8173
90; 90; 90
2376.63Majumdar, 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 CIFC29 H32 N2 S2P 1 21 110.39896; 9.11807; 13.7409
90; 108.291; 90
1237.06Majumdar, 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 CIFC21 H15 F O2P 1 21/c 112.0845; 5.9453; 22.597
90; 103.246; 90
1580.3Du, 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 CIFC32 H38 O5 Si2P 1 21/c 19.2692; 9.7098; 34.752
90; 92.266; 90
3125.3Zimmerman, 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 CIFC16 H17 Cl O5P -16.9648; 7.7685; 14.728
76.228; 76.658; 84.002
752.04Zimmerman, 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 CIFC18 H17 Br O5P 1 21 15.6762; 10.5443; 14.1611
90; 100.294; 90
833.92Sinha, 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 CIFC19 H20 N2 O6P 21 21 215.8624; 9.6327; 31.868
90; 90; 90
1799.61Chen, 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 CIFC22 H32 Cl2 I2 Si2P 1 21/n 113.1915; 9.4009; 22.0383
90; 106.275; 90
2623.49Sproul, 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 CIFC16 H10 Cl2 I2P b c a9.0806; 15.5457; 23.2185
90; 90; 90
3277.6Sproul, 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 CIFC26 H19 N3 O5 SP -110.4761; 10.8361; 11.3358
76.911; 61.867; 86.563
1103.68Rao, 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 CIFC20 H24 Cl N3 OP 1 21 110.868; 6.8325; 12.6102
90; 103.793; 90
909.38Johnson, 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 CIFC13 H17 Cl O3P n a 2128.508; 5.4891; 8.1976
90; 90; 90
1282.79Tanveer, 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 CIFC21 H21 Cl O4P b c a15.5081; 11.7102; 20.245
90; 90; 90
3676.6Tanveer, 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 CIFC33 H30 N2 O6 S2P -110.7946; 12.4093; 13.1553
76.627; 68.739; 81.216
1593.12Yan, 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 CIFC33 H27 N3 O13P -111.319; 12.665; 14.597
86.284; 86.306; 68.207
1937.1Chen, 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 CIFC41 H60 N8 O3 Ti2P 1 21/n 119.8643; 9.0349; 24.8875
90; 106.793; 90
4276.1Chen, 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 CIFC163 H221 N28 O13 Ti4P -119.976; 20.518; 21.236
89.583; 78.919; 76.303
8292Chen, 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 CIFC22 H20 N2 O3P -111.7148; 11.8534; 14.1205
110; 95.83; 100.677
1781.51Dörr, 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 CIFC22 H22 N2 O3P c a 2117.651; 15.5231; 13.7865
90; 90; 90
3777.48Dörr, 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 CIFC22 H20 N2 O3P 1 21/n 115.2406; 5.6664; 20.6863
90; 94.254; 90
1781.53Dörr, 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 CIFC20 H23 N O8P 21 21 218.7215; 11.3257; 19.217
90; 90; 90
1898.2Paladino, 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 CIFC15 H15 N3 O4P 1 21/n 111.4762; 7.95324; 16.5869
90; 107.894; 90
1440.7Wang, 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 CIFC44 H42 F6 N6 O7 S2P b c a21.512; 10.424; 40.881
90; 90; 90
9167Zhu, 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 CIFC28 H23 F3 N2 O3P -18.882; 10.743; 14.629
87; 76.43; 65.66
1234.8Zhu, 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 CIFC25 H34 N2 O9 SiP b c a10.3059; 20.6482; 25.5756
90; 90; 90
5442.4Cheng, 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 CIFC25 H31 N O3 S2P 1 21 16.6067; 19.709; 9.7407
90; 109.22; 90
1197.65Fernández-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 CIFC13 H13 Cl N2 O2 SP 1 21/c 115.767; 5.759; 15.721
90; 112.32; 90
1320.5Lu, 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 CIFC23 H21 N O3 S2P -17.667; 8.7269; 17.0497
88.1161; 89.15; 62.1966
1008.54Miura, 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 CIFC270 H372 B6 N8 O30C 1 2/c 152.579; 21.835; 29.598
90; 117.54; 90
30130Danjo, 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 CIFC28 H44 O4 Si2P 21 21 217.702; 13.1321; 27.4999
90; 90; 90
2781.4Shi, 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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