Crystallography Open Database

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4029271 CIFC16 H20 N2 O2P 1 21 18.5091; 5.3731; 16.347
90; 92.714; 90		746.6Vu, Van Ha; Louafi, Fadila; Girard, Nicolas; Marion, Ronan; Roisnel, Thierry; Dorcet, Vincent; Hurvois, Jean-Pierre
Electrochemical Access to 8-(1-Phenyl-ethyl)-1,4-dioxa-8-aza-spiro[4.5]decane-7-carbonitrile. Application to the Asymmetric Syntheses of (+)-Myrtine and Alkaloid (+)-241D.
The Journal of organic chemistry, 2014, 79, 3358-3373
4029272 CIFC16 H20 N2 O2P 1 21 18.9941; 7.718; 10.8751
90; 101.498; 90		739.76Vu, Van Ha; Louafi, Fadila; Girard, Nicolas; Marion, Ronan; Roisnel, Thierry; Dorcet, Vincent; Hurvois, Jean-Pierre
Electrochemical Access to 8-(1-Phenyl-ethyl)-1,4-dioxa-8-aza-spiro[4.5]decane-7-carbonitrile. Application to the Asymmetric Syntheses of (+)-Myrtine and Alkaloid (+)-241D.
The Journal of organic chemistry, 2014, 79, 3358-3373
4029273 CIFC17 H22 N2 O2P 21 21 216.8561; 12.1178; 18.7361
90; 90; 90		1556.61Vu, Van Ha; Louafi, Fadila; Girard, Nicolas; Marion, Ronan; Roisnel, Thierry; Dorcet, Vincent; Hurvois, Jean-Pierre
Electrochemical Access to 8-(1-Phenyl-ethyl)-1,4-dioxa-8-aza-spiro[4.5]decane-7-carbonitrile. Application to the Asymmetric Syntheses of (+)-Myrtine and Alkaloid (+)-241D.
The Journal of organic chemistry, 2014, 79, 3358-3373
4029274 CIFC21 H25 O5 PP 1 21 19.4518; 9.6464; 10.9137
90; 99.425; 90		981.63Weise, Christian F; Lauridsen, Vibeke H; Rambo, Raoní S; Iversen, Eva H; Olsen, Marie-Luise; Jørgensen, Karl Anker
Organocatalytic Access to Enantioenriched Dihydropyran Phosphonates via an Inverse-Electron-Demand Hetero-Diels-Alder Reaction.
The Journal of organic chemistry, 2014, 79, 3537-3546
4029275 CIFC20 H22 O4P 21 21 216.2585; 15.968; 17.0842
90; 90; 90		1707.32Weise, Christian F; Lauridsen, Vibeke H; Rambo, Raoní S; Iversen, Eva H; Olsen, Marie-Luise; Jørgensen, Karl Anker
Organocatalytic Access to Enantioenriched Dihydropyran Phosphonates via an Inverse-Electron-Demand Hetero-Diels-Alder Reaction.
The Journal of organic chemistry, 2014, 79, 3537-3546
4029276 CIFC20 H25 B Br N3 O8P -19.78; 10.383; 13.081
97.135; 110.846; 102.196		1184.1Suchý, Mojmír; Hudson, Robert H E
Pyrimidine-Fused Heterocyclic Frameworks Based on an N4-Arylcytosine Scaffold: Synthesis, Characterization, and PNA Oligomerization of the Fluorescent Cytosine Analogue 5,6-BenzopC.
The Journal of organic chemistry, 2014, 79, 3336-3347
4029277 CIFC30 H27 N O6P 1 21 16.1224; 12.237; 16.495
90; 99.471; 90		1219Chaplin, Jason H; Jackson, Kristal; White, Jonathan M; Flynn, Bernard L
Convergent Access to Polycyclic Cyclopentanoids from α,β-Unsaturated Acid Chlorides and Alkynes through a Reductive Coupling, Nazarov Cyclization Sequence.
The Journal of organic chemistry, 2014, 79, 3659-3664
4029278 CIFC15 H14 N4 OP 1 21 17.3446; 10.3043; 9.2757
90; 101.418; 90		688.1Xiong, Yang; Zhang, Xuxue; Huang, Tao; Cao, Song
Synthesis of N-(α-Fluorovinyl)azoles by the Reaction of Difluoroalkenes with Azoles.
The Journal of organic chemistry, 2014, 79, 6395-6402
4029279 CIFC14 H14 O3P 21 21 219.44; 9.863; 11.214
90; 90; 90		1044.1Taber, Douglass F; Paquette, Craig M
Synthesis of the pentacylic core of (+)-salvileucalin B.
The Journal of organic chemistry, 2014, 79, 3410-3413
4029280 CIFC22 H26 N2 O2P 1 21 19.144; 10.9927; 9.6418
90; 103.148; 90		943.76Selim, Khalid B; Martel, Arnaud; Laurent, Mathieu Y; Lhoste, Jérôme; Py, Sandrine; Dujardin, Gilles
Enantioselective Ruthenium-Catalyzed 1,3-Dipolar Cycloadditions between C-Carboalkoxy Ketonitrones and Methacrolein: Solvent Effect on Reaction Selectivity and Its Rational.
The Journal of organic chemistry, 2014, 79, 3414-3426
4029281 CIFC69 H57 N15P 6319.986; 19.986; 8.8105
90; 90; 120		3047.8Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029282 CIFC150 H90 N30R -3 :H15.319; 15.319; 44.673
90; 90; 120		9079Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029283 CIFC42 H42 N6P 1 21/c 111.366; 15.991; 9.664
90; 110.578; 90		1644.4Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029284 CIFC159 H42 N9R -3 :H20.221; 20.221; 38.779
90; 90; 120		13732Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029285 CIFC45 H45 N15P -110.491; 15.082; 15.571
62.847; 89.307; 77.513		2129.7Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029286 CIFC59 H45 Cl8 N18R -3 c :H15.098; 15.098; 94.97
90; 90; 120		18748Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029287 CIFC39 H39 N9C 1 m 17.6467; 24.339; 17.615
90; 94.85; 90		3266.6Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029288 CIFC141 H57 N15P -3 c 121.571; 21.571; 27.87
90; 90; 120		11231Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029289 CIFC160 H90 N30P -115.391; 18.883; 23.094
77.42; 87.51; 86.78		6537Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029290 CIFC36 H36 N12P -110.778; 12.792; 13.514
102.94; 111.17; 105.89		1559.1Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029291 CIFC36 H42 N18P 1 21/n 111.0322; 16.8447; 19.9205
90; 105.315; 90		3570.4Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029292 CIFC138 H78 N30R -3 :H15.21; 15.21; 44.815
90; 90; 120		8979Fa, Shi-Xin; Wang, Li-Xia; Wang, De-Xian; Zhao, Liang; Wang, Mei-Xiang
Synthesis, Structure, and Fullerene-Complexing Property of Azacalix[6]aromatics.
The Journal of organic chemistry, 2014, 79, 3559-3571
4029293 CIFC11 H19 O2C 1 c 112.655; 10.193; 8.544
90; 102.529; 90		1075.9Zhu, Jia-Liang; Wu, Sih-Ting; Shie, Jr-Yun
Access to Functionalized Bicyclo[4,3,0]nonenes via Palladium-Catalyzed Oxidative Cyclization of 2-Allylcyclohexyl Oximes.
The Journal of organic chemistry, 2014, 79, 3623-3633
4029294 CIFC19 H33 N O2 S Si2P 110.368; 10.478; 21.015
88.133; 89.305; 80.119		2247.9Kondo, Yasuhiro; Sasaki, Michiko; Kawahata, Masatoshi; Yamaguchi, Kentaro; Takeda, Kei
Enantioselective Synthesis of α-Silylamines by Meerwein-Ponndorf-Verley-Type Reduction of α-Silylimines by a Chiral Lithium Amide.
The Journal of organic chemistry, 2014, 79, 3601-3609
4029295 CIFC17 H23 N O2 S SiP 1 21 110.545; 9.535; 10.077
90; 115.62; 90		913.6Kondo, Yasuhiro; Sasaki, Michiko; Kawahata, Masatoshi; Yamaguchi, Kentaro; Takeda, Kei
Enantioselective Synthesis of α-Silylamines by Meerwein-Ponndorf-Verley-Type Reduction of α-Silylimines by a Chiral Lithium Amide.
The Journal of organic chemistry, 2014, 79, 3601-3609
4029296 CIFC23 H20 Cl F3 N2 O4P -17.844; 11.183; 12.865
85.56; 85.01; 80.27		1106Yang, Li-Jun; Li, Shen; Wang, Shuai; Nie, Jing; Ma, Jun-An
Nucleophilic lewis base dependent addition reactions of allenoates with trifluoromethylated cyclic ketimines.
The Journal of organic chemistry, 2014, 79, 3547-3558
4029297 CIFC23 H20 Cl F3 N2 O4P 1 21/c 110.062; 12.589; 18.91
90; 101.187; 90		2350Yang, Li-Jun; Li, Shen; Wang, Shuai; Nie, Jing; Ma, Jun-An
Nucleophilic lewis base dependent addition reactions of allenoates with trifluoromethylated cyclic ketimines.
The Journal of organic chemistry, 2014, 79, 3547-3558
4029298 CIFC9 H10 N2 O3P 21 21 218.7212; 9.3821; 11.148
90; 90; 90		912.2Thalluri, Kishore; Manne, Srinivasa Rao; Dev, Dharm; Mandal, Bhubaneswar
Ethyl 2-Cyano-2-(4-nitrophenylsulfonyloxyimino)acetate-Mediated Lossen Rearrangement: Single-Pot Racemization-Free Synthesis of Hydroxamic Acids and Ureas from Carboxylic Acids.
The Journal of organic chemistry, 2014, 79, 3765-3775
4029299 CIFC34 H30 N2 O9P 1 21/c 19.046; 11.3528; 30.038
90; 98.656; 90		3049.7Gao, Hong; Sun, Jing; Yan, Chao-Guo
Selective Synthesis of Functionalized Spiro[indoline-3,2'-pyridines] and Spiro[indoline-3,4'-pyridines] by Lewis Acid Catalyzed Reactions of Acetylenedicarboxylate, Arylamines, and Isatins.
The Journal of organic chemistry, 2014, 79, 4131-4136
4029300 CIFC38 H38 N2 O9P -110.2438; 13.8664; 14.1071
105.457; 108.034; 98.027		1781.7Gao, Hong; Sun, Jing; Yan, Chao-Guo
Selective Synthesis of Functionalized Spiro[indoline-3,2'-pyridines] and Spiro[indoline-3,4'-pyridines] by Lewis Acid Catalyzed Reactions of Acetylenedicarboxylate, Arylamines, and Isatins.
The Journal of organic chemistry, 2014, 79, 4131-4136
4029301 CIFC27 H24 N2 O10P -111.2385; 11.278; 11.737
113.393; 92.165; 102.263		1321.8Gao, Hong; Sun, Jing; Yan, Chao-Guo
Selective Synthesis of Functionalized Spiro[indoline-3,2'-pyridines] and Spiro[indoline-3,4'-pyridines] by Lewis Acid Catalyzed Reactions of Acetylenedicarboxylate, Arylamines, and Isatins.
The Journal of organic chemistry, 2014, 79, 4131-4136
4029302 CIFC15 H9 Cl F5 N S SeP n m a12.536; 6.7909; 18.646
90; 90; 90		1587.3Hua, Guoxiong; Du, Junyi; Slawin, Alexandra M. Z.; Woollins, J. Derek
2,4-Diaryl-1,3-Chalcogen Azoles Bearing Pentafluorosulfanyl SF5 Groups: A Synthetic and Structural Study.
The Journal of organic chemistry, 2014, 79, 3876-3886
4029303 CIFC15 H9 F5 N2 O2 S SeP 21 21 216.761; 12.748; 18.642
90; 90; 90		1606.7Hua, Guoxiong; Du, Junyi; Slawin, Alexandra M. Z.; Woollins, J. Derek
2,4-Diaryl-1,3-Chalcogen Azoles Bearing Pentafluorosulfanyl SF5 Groups: A Synthetic and Structural Study.
The Journal of organic chemistry, 2014, 79, 3876-3886
4029304 CIFC17 H14 F5 N O2 S2P 1 21/c 112.075; 9.345; 16.111
90; 106.76; 90		1741Hua, Guoxiong; Du, Junyi; Slawin, Alexandra M. Z.; Woollins, J. Derek
2,4-Diaryl-1,3-Chalcogen Azoles Bearing Pentafluorosulfanyl SF5 Groups: A Synthetic and Structural Study.
The Journal of organic chemistry, 2014, 79, 3876-3886
4029305 CIFC16 H12 F5 N O S SeC 1 2/c 135.77; 6.207; 15.93
90; 107.028; 90		3382Hua, Guoxiong; Du, Junyi; Slawin, Alexandra M. Z.; Woollins, J. Derek
2,4-Diaryl-1,3-Chalcogen Azoles Bearing Pentafluorosulfanyl SF5 Groups: A Synthetic and Structural Study.
The Journal of organic chemistry, 2014, 79, 3876-3886
4029306 CIFC15 H9 F5 N2 O2 S SeP -17.911; 10.425; 11.609
109.181; 109.088; 100.49		808Hua, Guoxiong; Du, Junyi; Slawin, Alexandra M. Z.; Woollins, J. Derek
2,4-Diaryl-1,3-Chalcogen Azoles Bearing Pentafluorosulfanyl SF5 Groups: A Synthetic and Structural Study.
The Journal of organic chemistry, 2014, 79, 3876-3886
4029307 CIFC17 H14 F5 N O2 S SeP -19.65; 12.717; 15.93
77.557; 75.918; 77.43		1823.2Hua, Guoxiong; Du, Junyi; Slawin, Alexandra M. Z.; Woollins, J. Derek
2,4-Diaryl-1,3-Chalcogen Azoles Bearing Pentafluorosulfanyl SF5 Groups: A Synthetic and Structural Study.
The Journal of organic chemistry, 2014, 79, 3876-3886
4029308 CIFC16 H12 F5 N S SeP n a 217.789; 33.34; 6.278
90; 90; 90		1630Hua, Guoxiong; Du, Junyi; Slawin, Alexandra M. Z.; Woollins, J. Derek
2,4-Diaryl-1,3-Chalcogen Azoles Bearing Pentafluorosulfanyl SF5 Groups: A Synthetic and Structural Study.
The Journal of organic chemistry, 2014, 79, 3876-3886
4029309 CIFC21 H32 N2 O3 SP 21 21 219.0021; 14.9816; 16.5464
90; 90; 90		2231.5Bosque, Irene; Gonzalez-Gomez, Jose C; Loza, María Isabel; Brea, José
Natural Tetraponerines: A General Synthesis and Antiproliferative Activity.
The Journal of organic chemistry, 2014, 79, 3982-3991
4029310 CIFC34 H31 Cl N2 O9 SP -19.9316; 13.506; 14.3545
106.446; 105.813; 103.488		1673.27Qiu, Lin; Gao, Lixin; Tang, Jixing; Wang, Dongwei; Guo, Xin; Liu, Shunying; Yang, Liping; Li, Jia; Hu, Wenhao
Regio- and Diastereoselective Construction of α-Hydroxy-δ-amino Ester Derivatives via 1,4-Conjugate Addition of β,γ-Unsaturated N-Sulfonylimines.
The Journal of organic chemistry, 2014, 79, 4142-4147
4029311 CIFC22 H18 Cl2 N2 O2P 1 21/n 114.8608; 7.7619; 17.4366
90; 106.782; 90		1925.62Wang, Chengjin; Xing, Dong; Wang, Dongwei; Wu, Xiang; Hu, Wenhao
Synthesis of 3-Amino-3-hydroxymethyloxindoles and 3-Hydroxy-3-hydroxymethyloxindoles by Rh2(OAc)4-Catalyzed Three-Component Reactions of 3-Diazooxindoles with Formaldehyde and Anilines or Water.
The Journal of organic chemistry, 2014, 79, 3908-3916
4029312 CIFC18 H16 O2P 1 21/c 112.3796; 10.5493; 11.3168
90; 106.991; 90		1413.4Ghosh, Priya; Saha, Pipas; Bondalapati, Somasekhar; Indukuri, Kiran; Saikia, Anil K.
Lewis Acid Mediated Intramolecular C-C Bond Formation of Alkyne-Epoxide Leading to Six-Membered Nitrogen and Oxygen Heterocycles.
The Journal of organic chemistry, 2014, 79, 4119-4124
4029313 CIFC22 H17 N O3 SP 1 21/c 15.587; 18.446; 17.936
90; 97.283; 90		1833.5Zhang, Peng; Cook, Andrea M.; Liu, Yang; Wolf, Christian
Copper(I)-Catalyzed Nucleophilic Addition of Ynamides to Acyl Chlorides and Activated N-Heterocycles.
The Journal of organic chemistry, 2014, 79, 4167-4173
4029314 CIFC12 H14 N2 O7P 1 21 112.8822; 9.5928; 22.444
90; 103.587; 90		2695.9Pandey, Anil K.; Yap, Glenn P. A.; Zondlo, Neal J.
(2S,4R)-4-Hydroxyproline(4-nitrobenzoate): Strong Induction of Stereoelectronic Effects via a Readily Synthesized Proline Derivative. Crystallographic Observation of a Correlation between Torsion Angle and Bond Length in a Hyperconjugative Interaction.
The Journal of organic chemistry, 2014, 79, 4174-4179
4029315 CIFC14 H27 F2 N O6 SP 1 21 112.221; 6.0654; 13.752
90; 96.378; 90		1013.1Fontenelle, Clément Q; Conroy, Matthew; Light, Mark; Poisson, Thomas; Pannecoucke, Xavier; Linclau, Bruno
Stereoselectivity of the Honda-Reformatsky Reaction in Reactions with Ethyl Bromodifluoroacetate with α-Oxygenated Sulfinylimines.
The Journal of organic chemistry, 2014, 79, 4186-4195
4029316 CIFC9 H17 F2 N O3 SP 1 21 15.742; 17.689; 6.193
90; 100.655; 90		618.2Fontenelle, Clément Q; Conroy, Matthew; Light, Mark; Poisson, Thomas; Pannecoucke, Xavier; Linclau, Bruno
Stereoselectivity of the Honda-Reformatsky Reaction in Reactions with Ethyl Bromodifluoroacetate with α-Oxygenated Sulfinylimines.
The Journal of organic chemistry, 2014, 79, 4186-4195
4029317 CIFC14 H25 F2 N O5 SP 21 21 218.329; 9.292; 23.43
90; 90; 90		1813Fontenelle, Clément Q; Conroy, Matthew; Light, Mark; Poisson, Thomas; Pannecoucke, Xavier; Linclau, Bruno
Stereoselectivity of the Honda-Reformatsky Reaction in Reactions with Ethyl Bromodifluoroacetate with α-Oxygenated Sulfinylimines.
The Journal of organic chemistry, 2014, 79, 4186-4195
4029318 CIFC33 H32 N4 PdP -16.494; 10.683; 19.0024
91.402; 91.845; 102.929		1283.53Li, Ruoshi; Lammer, Aaron D.; Ferrence, Gregory M.; Lash, Timothy D.
Synthesis, Structural Characterization, Aromatic Characteristics, and Metalation of Neo-Confused Porphyrins, a Newly Discovered Class of Porphyrin Isomers.
The Journal of organic chemistry, 2014, 79, 4078-4093
4029319 CIFC30 H30 N4 O2 PdP -18.1266; 10.9322; 14.5533
105.58; 91.632; 97.148		1233.16Li, Ruoshi; Lammer, Aaron D.; Ferrence, Gregory M.; Lash, Timothy D.
Synthesis, Structural Characterization, Aromatic Characteristics, and Metalation of Neo-Confused Porphyrins, a Newly Discovered Class of Porphyrin Isomers.
The Journal of organic chemistry, 2014, 79, 4078-4093
4029320 CIFC30 H30 N4 Ni O2P -18.1062; 10.8971; 28.0896
83.679; 85.737; 82.79		2442.07Li, Ruoshi; Lammer, Aaron D.; Ferrence, Gregory M.; Lash, Timothy D.
Synthesis, Structural Characterization, Aromatic Characteristics, and Metalation of Neo-Confused Porphyrins, a Newly Discovered Class of Porphyrin Isomers.
The Journal of organic chemistry, 2014, 79, 4078-4093
4029321 CIFC33 H34 N4P -110.6439; 11.4507; 12.7871
88.093; 67.922; 64.645		1289.84Li, Ruoshi; Lammer, Aaron D.; Ferrence, Gregory M.; Lash, Timothy D.
Synthesis, Structural Characterization, Aromatic Characteristics, and Metalation of Neo-Confused Porphyrins, a Newly Discovered Class of Porphyrin Isomers.
The Journal of organic chemistry, 2014, 79, 4078-4093
4029322 CIFC21 H30 N2 O4P 21 21 218.3186; 12.4731; 19.1532
90; 90; 90		1987.3Rallapalli, Sundari K.; Namjoshi, Ojas A.; Tiruveedhula, V. V. N. Phani Babu; Deschamps, Jeffrey R.; Cook, James M.
Stereospecific Total Synthesis of the Indole Alkaloid Ervincidine. Establishment of the C-6 Hydroxyl Stereochemistry.
The Journal of organic chemistry, 2014, 79, 3776-3780
4029323 CIFC19 H20 N2 O2P 21 21 219.6247; 11.6485; 13.7072
90; 90; 90		1536.76Rallapalli, Sundari K.; Namjoshi, Ojas A.; Tiruveedhula, V. V. N. Phani Babu; Deschamps, Jeffrey R.; Cook, James M.
Stereospecific Total Synthesis of the Indole Alkaloid Ervincidine. Establishment of the C-6 Hydroxyl Stereochemistry.
The Journal of organic chemistry, 2014, 79, 3776-3780
4029328 CIFC15 H18 O2P c c n16.9949; 21.083; 7.3381
90; 90; 90		2629.3Sun, Ning; Chen, Ming; Liu, Yuanhong
Gold-Catalyzed Oxidative Reactions of Propargylic Carbonates Involving 1,2-Carbonate Migration: Stereoselective Synthesis of Functionalized Alkenes.
The Journal of organic chemistry, 2014, 79, 4055-4067
4029329 CIFC20 H18 O3P 1 21/c 115.191; 7.0358; 16.337
90; 115.321; 90		1578.4Sun, Ning; Chen, Ming; Liu, Yuanhong
Gold-Catalyzed Oxidative Reactions of Propargylic Carbonates Involving 1,2-Carbonate Migration: Stereoselective Synthesis of Functionalized Alkenes.
The Journal of organic chemistry, 2014, 79, 4055-4067
4029330 CIFC15 H18 O4C 1 2/c 123.655; 9.7505; 15.4692
90; 126.057; 90		2884.4Sun, Ning; Chen, Ming; Liu, Yuanhong
Gold-Catalyzed Oxidative Reactions of Propargylic Carbonates Involving 1,2-Carbonate Migration: Stereoselective Synthesis of Functionalized Alkenes.
The Journal of organic chemistry, 2014, 79, 4055-4067
4029331 CIFC39 H24 N2P -18.078; 12.824; 13.714
113.32; 98.37; 95.61		1271.7Zheng, Liyao; Hua, Ruimao
Modular Assembly of Ring-Fused and π-Extended Phenanthroimidazoles via C-H Activation and Alkyne Annulation.
The Journal of organic chemistry, 2014, 79, 3930-3936
4029332 CIFC35 H22 N2P -19.635; 10.0387; 12.277
83.666; 88.781; 89.717		1179.9Zheng, Liyao; Hua, Ruimao
Modular Assembly of Ring-Fused and π-Extended Phenanthroimidazoles via C-H Activation and Alkyne Annulation.
The Journal of organic chemistry, 2014, 79, 3930-3936
4029333 CIFC31 H24 N2 OP -112.4433; 14.26; 15.249
68.103; 67.336; 70.436		2258.3Zheng, Liyao; Hua, Ruimao
Modular Assembly of Ring-Fused and π-Extended Phenanthroimidazoles via C-H Activation and Alkyne Annulation.
The Journal of organic chemistry, 2014, 79, 3930-3936
4029334 CIFC30 H20 N2P -19.114; 9.534; 11.901
96.66; 99.74; 93.8		1008.4Zheng, Liyao; Hua, Ruimao
Modular Assembly of Ring-Fused and π-Extended Phenanthroimidazoles via C-H Activation and Alkyne Annulation.
The Journal of organic chemistry, 2014, 79, 3930-3936
4029335 CIFC21 H17 N O4P 1 21/n 110.976; 9.914; 15.781
90; 103.62; 90		1668.9Sun, Jinwei; Wang, Fuyao; Hu, Huayou; Wang, Xiangshan; Wu, Hui; Liu, Yun
Copper(II)-Catalyzed Carbon-Carbon Triple Bond Cleavage of Internal Alkynes for the Synthesis of Annulated Indolizines.
The Journal of organic chemistry, 2014, 79, 3992-3998
4029336 CIFC23 H19 N3 O3 SP 1 21/c 15.817; 34.7466; 9.9049
90; 101.37; 90		1962.7Cantillo, David; Avalos, Martín; Babiano, Reyes; Cintas, Pedro; Jiménez, José L; Light, Mark E.; Palacios, Juan C.; Porro, Rocío
Stepwise Formation of 1,3-Diazolium-4-thiolates by Münchnone Cycloadditions: Promising Candidates for Nonlinear Optics.
The Journal of organic chemistry, 2014, 79, 4201-4205
4029337 CIFC24 H21 N3 O4 SP 1 21/c 112.2636; 9.7059; 18.4895
90; 101.565; 90		2156.11Cantillo, David; Avalos, Martín; Babiano, Reyes; Cintas, Pedro; Jiménez, José L; Light, Mark E.; Palacios, Juan C.; Porro, Rocío
Stepwise Formation of 1,3-Diazolium-4-thiolates by Münchnone Cycloadditions: Promising Candidates for Nonlinear Optics.
The Journal of organic chemistry, 2014, 79, 4201-4205
4029338 CIFC28 H26 N2 O4P -19.8381; 10.4824; 12.5322
74.656; 74.429; 71.299		1156.45Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029339 CIFC26 H20 Br2 N2 O2P 1 21/n 19.3468; 14.5715; 16.6456
90; 105.26; 90		2187.15Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029340 CIFC26 H21 N O4P 21 21 218.6359; 12.0457; 19.5543
90; 90; 90		2034.15Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029341 CIFC28 H19 N O2P 1 21/n 110.8929; 8.6496; 21.3698
90; 95.896; 90		2002.8Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029342 CIFC32 H24 N2 O2P -19.765; 11.9476; 12.3011
113.172; 101.293; 106.109		1189.59Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029343 CIFC44 H33 N3 O2P -18.502; 11.6522; 17.4372
104.952; 92.109; 98.182		1647.09Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029344 CIFC26 H22 N2 O2P -18.7939; 9.6279; 12.566
76.008; 78.669; 85.631		1011.77Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029345 CIFC25 H19 N O3P -110.0356; 12.8316; 16.3402
80.535; 80.757; 74.556		1985.42Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029346 CIFC28 H19 N O4P -18.1852; 8.4437; 16.921
97.887; 93.333; 111.291		1071.93Thapaliya, Ek Raj; Captain, Burjor; Raymo, Françisco M
Photoactivatable Anthracenes.
The Journal of organic chemistry, 2014, 79, 3973-3981
4029347 CIFC38 H30 N6P n a 2120.109; 12.9225; 12.0941
90; 90; 90		3142.8Jiang, Bo; Ning, Yi; Fan, Wei; Tu, Shu-Jiang; Li, Guigen
Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles.
The Journal of organic chemistry, 2014, 79, 4018-4024
4029348 CIFC20 H16 I2 N6P 1 21/n 18.4458; 10.7913; 11.4138
90; 91.973; 90		1039.65Jiang, Bo; Ning, Yi; Fan, Wei; Tu, Shu-Jiang; Li, Guigen
Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles.
The Journal of organic chemistry, 2014, 79, 4018-4024
4029349 CIFC26 H24 Cl N O6 SP 1 21 113.9947; 5.8914; 15.0886
90; 97.064; 90		1234.59Arakawa, Yukihiro; Fritz, Sven P.; Wennemers, Helma
Organocatalytic Stereoselective Synthesis of Acyclic γ-Nitrothioesters with All-Carbon Quaternary Stereogenic Centers.
The Journal of organic chemistry, 2014, 79, 3937-3945
4029350 CIFC18 H19 N O4 SP 21 21 215.7422; 10.5827; 28.156
90; 90; 90		1711Arakawa, Yukihiro; Fritz, Sven P.; Wennemers, Helma
Organocatalytic Stereoselective Synthesis of Acyclic γ-Nitrothioesters with All-Carbon Quaternary Stereogenic Centers.
The Journal of organic chemistry, 2014, 79, 3937-3945
4029351 CIFC18 H18 Cl N O4 SP 1 21 110.069; 5.823; 17.107
90; 106.319; 90		962.6Arakawa, Yukihiro; Fritz, Sven P.; Wennemers, Helma
Organocatalytic Stereoselective Synthesis of Acyclic γ-Nitrothioesters with All-Carbon Quaternary Stereogenic Centers.
The Journal of organic chemistry, 2014, 79, 3937-3945
4029352 CIFC15 H17 Br N2 O3P 21 21 217.7315; 14.3537; 26.576
90; 90; 90		2949.3Boucherif, Amina; Yang, Qing-Qing; Wang, Qiang; Chen, Jia-Rong; Lu, Liang-Qiu; Xiao, Wen-Jing
Enantio- and Diastereoselective Synthesis of Spiro-epoxyoxindoles.
The Journal of organic chemistry, 2014, 79, 3924-3929
4029353 CIFC7 H6 N4 SP -13.8592; 8.4044; 12.5408
87.517; 85.342; 81.578		400.83Koyioni, Maria; Manoli, Maria; Manolis, Manos J.; Koutentis, Panayiotis A.
Reinvestigating the Reaction of 1H-Pyrazol-5-amines with 4,5-Dichloro-1,2,3-dithiazolium Chloride: A Route to Pyrazolo[3,4-c]isothiazoles and Pyrazolo[3,4-d]thiazoles.
The Journal of organic chemistry, 2014, 79, 4025-4037
4029354 CIFC14 H12 Cl2 N8 S5C 1 2/c 134.721; 4.0036; 14.975
90; 100.148; 90		2049.1Koyioni, Maria; Manoli, Maria; Manolis, Manos J.; Koutentis, Panayiotis A.
Reinvestigating the Reaction of 1H-Pyrazol-5-amines with 4,5-Dichloro-1,2,3-dithiazolium Chloride: A Route to Pyrazolo[3,4-c]isothiazoles and Pyrazolo[3,4-d]thiazoles.
The Journal of organic chemistry, 2014, 79, 4025-4037
4029355 CIFC16 H14 Cl3 N9 S5P -110.449; 12.6255; 21.3511
97.143; 92.352; 93.441		2786.5Koyioni, Maria; Manoli, Maria; Manolis, Manos J.; Koutentis, Panayiotis A.
Reinvestigating the Reaction of 1H-Pyrazol-5-amines with 4,5-Dichloro-1,2,3-dithiazolium Chloride: A Route to Pyrazolo[3,4-c]isothiazoles and Pyrazolo[3,4-d]thiazoles.
The Journal of organic chemistry, 2014, 79, 4025-4037
4029356 CIFC30 H20 N2 OP -110.4838; 14.518; 15.9147
79.164; 73.907; 71.712		2196.2Allu, Srinivasarao; Swamy, K. C. Kumara
Ruthenium-Catalyzed Synthesis of Isoquinolones with 8-Aminoquinoline as a Bidentate Directing Group in C-H Functionalization.
The Journal of organic chemistry, 2014, 79, 3963-3972
4029357 CIFC22 H20 N2 OP 1 21/c 113.1006; 14.6841; 8.7923
90; 100.348; 90		1663.9Allu, Srinivasarao; Swamy, K. C. Kumara
Ruthenium-Catalyzed Synthesis of Isoquinolones with 8-Aminoquinoline as a Bidentate Directing Group in C-H Functionalization.
The Journal of organic chemistry, 2014, 79, 3963-3972
4029358 CIFC25 H18 N2 OP -17.4501; 8.7551; 14.931
95.2; 98.89; 103.19		928.8Allu, Srinivasarao; Swamy, K. C. Kumara
Ruthenium-Catalyzed Synthesis of Isoquinolones with 8-Aminoquinoline as a Bidentate Directing Group in C-H Functionalization.
The Journal of organic chemistry, 2014, 79, 3963-3972
4029359 CIFC31 H21 N3 O3P 1 21/n 19.5537; 16.927; 15.612
90; 105.52; 90		2432.6Allu, Srinivasarao; Swamy, K. C. Kumara
Ruthenium-Catalyzed Synthesis of Isoquinolones with 8-Aminoquinoline as a Bidentate Directing Group in C-H Functionalization.
The Journal of organic chemistry, 2014, 79, 3963-3972
4029360 CIFC26 H25 Cl N2 O RuP 21 21 217.8508; 15.8682; 18.2984
90; 90; 90		2279.58Allu, Srinivasarao; Swamy, K. C. Kumara
Ruthenium-Catalyzed Synthesis of Isoquinolones with 8-Aminoquinoline as a Bidentate Directing Group in C-H Functionalization.
The Journal of organic chemistry, 2014, 79, 3963-3972
4029361 CIFC9 H16 N2 O3P 1 21/c 19.561; 10.152; 21.593
90; 96.807; 90		2081.1Zhou, Jing; Yeung, Ying-Yeung
Synthesis of Reboxetine Intermediate and Carnitine Acetyltransferase Inhibitor via NBS-Induced Electrophilic Multicomponent Reaction.
The Journal of organic chemistry, 2014, 79, 4644-4649
4029362 CIFC11 H13 Cl N2 O5 SP -17.3876; 9.7133; 10.4673
103.383; 104.427; 104.585		668.4Zhou, Jing; Yeung, Ying-Yeung
Synthesis of Reboxetine Intermediate and Carnitine Acetyltransferase Inhibitor via NBS-Induced Electrophilic Multicomponent Reaction.
The Journal of organic chemistry, 2014, 79, 4644-4649
4029363 CIFC22 H16 Cl N3 OP 1 21 19.038; 12.131; 9.119
90; 113.364; 90		917.8Wang, Ying-Chun; Xie, Yu-Yang; Qu, Hong-En; Wang, Heng-Shan; Pan, Ying-Ming; Huang, Fu-Ping
Ce(OTf)3-Catalyzed [3 + 2] Cycloaddition of Azides with Nitroolefins: Regioselective Synthesis of 1,5-Disubstituted 1,2,3-Triazoles.
The Journal of organic chemistry, 2014, 79, 4463-4469
4029364 CIFC15 H13 N3 OP 1 21/c 126.329; 10.877; 18.902
90; 102.757; 90		5280Wang, Ying-Chun; Xie, Yu-Yang; Qu, Hong-En; Wang, Heng-Shan; Pan, Ying-Ming; Huang, Fu-Ping
Ce(OTf)3-Catalyzed [3 + 2] Cycloaddition of Azides with Nitroolefins: Regioselective Synthesis of 1,5-Disubstituted 1,2,3-Triazoles.
The Journal of organic chemistry, 2014, 79, 4463-4469
4029365 CIFC51.5 H57 D6 N7 O9.5P 1 21/c 121.423; 9.312; 25.48
90; 101.743; 90		4976.6De Poli, Matteo; Byrne, Liam; Brown, Robert A.; Solà, Jordi; Castellanos, Alejandro; Boddaert, Thomas; Wechsel, Romina; Beadle, Jonathan D.; Clayden, Jonathan
Engineering the Structure of an N-Terminal β-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.
The Journal of organic chemistry, 2014, 79, 4659-4675
4029366 CIFC30 H58 N8 O10P 1 21 19.6099; 14.0444; 14.4849
90; 98.63; 90		1932.82De Poli, Matteo; Byrne, Liam; Brown, Robert A.; Solà, Jordi; Castellanos, Alejandro; Boddaert, Thomas; Wechsel, Romina; Beadle, Jonathan D.; Clayden, Jonathan
Engineering the Structure of an N-Terminal β-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.
The Journal of organic chemistry, 2014, 79, 4659-4675
4029367 CIFC36 H62 N8 O11P 21 21 218.939; 15.0463; 64.8154
90; 90; 90		8717.6De Poli, Matteo; Byrne, Liam; Brown, Robert A.; Solà, Jordi; Castellanos, Alejandro; Boddaert, Thomas; Wechsel, Romina; Beadle, Jonathan D.; Clayden, Jonathan
Engineering the Structure of an N-Terminal β-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.
The Journal of organic chemistry, 2014, 79, 4659-4675
4029368 CIFC26 H49 N7 O9P 1 21 116.7586; 11.7537; 17.0863
90; 94.951; 90		3353.03De Poli, Matteo; Byrne, Liam; Brown, Robert A.; Solà, Jordi; Castellanos, Alejandro; Boddaert, Thomas; Wechsel, Romina; Beadle, Jonathan D.; Clayden, Jonathan
Engineering the Structure of an N-Terminal β-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.
The Journal of organic chemistry, 2014, 79, 4659-4675
4029369 CIFC32 H50 N6 O7P 21 21 218.186; 18.89; 22.446
90; 90; 90		3471De Poli, Matteo; Byrne, Liam; Brown, Robert A.; Solà, Jordi; Castellanos, Alejandro; Boddaert, Thomas; Wechsel, Romina; Beadle, Jonathan D.; Clayden, Jonathan
Engineering the Structure of an N-Terminal β-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.
The Journal of organic chemistry, 2014, 79, 4659-4675
4029370 CIFC27 H52 N8 O8P 1 21 111.5859; 9.585; 16.5938
90; 108.615; 90		1746.35De Poli, Matteo; Byrne, Liam; Brown, Robert A.; Solà, Jordi; Castellanos, Alejandro; Boddaert, Thomas; Wechsel, Romina; Beadle, Jonathan D.; Clayden, Jonathan
Engineering the Structure of an N-Terminal β-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.
The Journal of organic chemistry, 2014, 79, 4659-4675
4029371 CIFC33 H46 N6 O7P 111.357; 16.271; 18.895
80.846; 87.004; 89.866		3442.4De Poli, Matteo; Byrne, Liam; Brown, Robert A.; Solà, Jordi; Castellanos, Alejandro; Boddaert, Thomas; Wechsel, Romina; Beadle, Jonathan D.; Clayden, Jonathan
Engineering the Structure of an N-Terminal β-Turn To Maximize Screw-Sense Preference in Achiral Helical Peptide Chains.
The Journal of organic chemistry, 2014, 79, 4659-4675
4029372 CIFC46 H26 N2 S2P -110.3831; 13.0198; 13.2997
81.765; 78.203; 70.812		1656.55Li, Junbo; Li, Peizhou; Wu, Jiansheng; Gao, Junkuo; Xiong, Wei-Wei; Zhang, Guodong; Zhao, Yanli; Zhang, Qichun
[4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly.
The Journal of organic chemistry, 2014, 79, 4438-4445
4029373 CIFC48 H28 N4C 1 2/c 126.9975; 14.9487; 16.8201
90; 99.47; 90		6695.7Li, Junbo; Li, Peizhou; Wu, Jiansheng; Gao, Junkuo; Xiong, Wei-Wei; Zhang, Guodong; Zhao, Yanli; Zhang, Qichun
[4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly.
The Journal of organic chemistry, 2014, 79, 4438-4445
4029374 CIFC51 H32 Cl2 N2P -110.9885; 11.6518; 15.3264
85.393; 89.268; 73.761		1877.85Li, Junbo; Li, Peizhou; Wu, Jiansheng; Gao, Junkuo; Xiong, Wei-Wei; Zhang, Guodong; Zhao, Yanli; Zhang, Qichun
[4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly.
The Journal of organic chemistry, 2014, 79, 4438-4445
4029375 CIFC17 H14 Cl N O3P 21 21 217.1652; 12.6049; 16.4098
90; 90; 90		1482.08Wu, Xiang; Li, Ming-Li; Chen, Dian-Feng; Chen, Shu-Sen
Enantioselective construction of [6,5,6]-carbocyclic systems by organo/metal-catalyzed sequential reactions.
The Journal of organic chemistry, 2014, 79, 4743-4750
4029376 CIFC13 H17 N O2P c a 2119.234; 5.6695; 10.7313
90; 90; 90		1170.2Shimizu, Tomoaki; Koya, Shunsuke; Yamasaki, Ryu; Mutoh, Yuichiro; Azumaya, Isao; Katagiri, Kosuke; Saito, Shinichi
Acid-Mediated Ring-Expansion Reaction of N-Aryl-2-vinylazetidines: Synthesis and Unanticipated Reactivity of Tetrahydrobenzazocines.
The Journal of organic chemistry, 2014, 79, 4367-4377
4029377 CIFC13 H17 N O2P 1 21/c 111.401; 12; 8.479
90; 92.305; 90		1159.1Shimizu, Tomoaki; Koya, Shunsuke; Yamasaki, Ryu; Mutoh, Yuichiro; Azumaya, Isao; Katagiri, Kosuke; Saito, Shinichi
Acid-Mediated Ring-Expansion Reaction of N-Aryl-2-vinylazetidines: Synthesis and Unanticipated Reactivity of Tetrahydrobenzazocines.
The Journal of organic chemistry, 2014, 79, 4367-4377
4029378 CIFC27 H19 N O2P -15.7246; 10.9332; 16.289
77.753; 86.78; 80.766		983.1Wang, Meining; Zhang, Chi; Sun, Li-Ping; Ding, Chunyong; Zhang, Ao
Naphthoquinone-directed C-h annulation and csp(3)-h bond cleavage: one-pot synthesis of tetracyclic naphthoxazoles.
The Journal of organic chemistry, 2014, 79, 4553-4560
4029379 CIFC38 H40 Br2 Cl4 N4 O4P 1 21/c 112.7758; 12.4749; 24.7006
90; 96.782; 90		3909.2DeBlase, Catherine R.; Finke, Ryan T.; Porras, Jonathan A.; Tanski, Joseph M.; Nadeau, Jocelyn M.
C-Shaped Diastereomers Containing Cofacial Thiophene-Substituted Quinoxaline Rings: Synthesis, Photophysical Properties, and X-ray Crystallography.
The Journal of organic chemistry, 2014, 79, 4312-4321
4029380 CIFC42 H36 Cl8 N4 O4 S2P -110.5303; 11.5381; 18.5812
86.903; 74.816; 77.042		2123.3DeBlase, Catherine R.; Finke, Ryan T.; Porras, Jonathan A.; Tanski, Joseph M.; Nadeau, Jocelyn M.
C-Shaped Diastereomers Containing Cofacial Thiophene-Substituted Quinoxaline Rings: Synthesis, Photophysical Properties, and X-ray Crystallography.
The Journal of organic chemistry, 2014, 79, 4312-4321
4029381 CIFC41 H33 Cl7 N4 O4 S2P 1 21/n 111.149; 32.7727; 11.5886
90; 98.527; 90		4187.5DeBlase, Catherine R.; Finke, Ryan T.; Porras, Jonathan A.; Tanski, Joseph M.; Nadeau, Jocelyn M.
C-Shaped Diastereomers Containing Cofacial Thiophene-Substituted Quinoxaline Rings: Synthesis, Photophysical Properties, and X-ray Crystallography.
The Journal of organic chemistry, 2014, 79, 4312-4321
4029382 CIFC34 H26 OP -19.14; 11.564; 11.837
81.82; 89.37; 73.3		1185.6Guo, Biao; Zheng, Liyao; Yang, Lichen; Hua, Ruimao
Synthesis of Chrysene Derivatives via Copper-Catalyzed One-Pot Dimerization of 2-Alkynyl-1-acetylbenzenes.
The Journal of organic chemistry, 2014, 79, 4352-4357
4029383 CIFC23 H21 N OP -15.6805; 10.0159; 15.1868
91.566; 97.711; 96.58		849.8Chen, Jian-Ming; Chang, Chin-Jung; Ke, Yao-Jin; Liu, Rai-Shung
Catalytic Formal [4 + 2] Cycloadditions between Unactivated Allenes and N-Hydroxyaniline Catalyzed by AuCl3/CuCl2/O2.
The Journal of organic chemistry, 2014, 79, 4306-4311
4029384 CIFC34 H38 N2 OI 1 2/a 145.341; 6.3267; 19.1637
90; 94.165; 90		5482.8Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029385 CIFC33 H34 Cl2 O5P -19.3084; 11.0123; 14.2584
96.174; 92.581; 96.04		1442.7Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029386 CIFC34 H32 F6 N2 OC 1 2/c 134.0554; 9.9336; 23.0128
90; 129.512; 90		6006.1Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029387 CIFC32 H30 O4P 1 21/n 19.568; 9.0894; 28.1687
90; 95.888; 90		2436.83Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029388 CIFC36 H38 O8C 1 2/c 127.2623; 7.994; 18.8173
90; 130.377; 90		3124.1Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029389 CIFC32 H24 F6 O2P 1 21/c 116.1001; 19.841; 17.6455
90; 115.919; 90		5069.7Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029390 CIFC34 H38 N2 O3P b c a21.8256; 10.1693; 25.5637
90; 90; 90		5673.9Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029391 CIFC34 H34 O6P -19.148; 12.84; 13.415
107.886; 101.844; 92.212		1458.9Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029392 CIFC32 H26 Br2 O4P -19.8125; 11.0615; 13.6335
70.815; 78.876; 81.967		1366.69Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029393 CIFC38 H44 O3P 1 21/c 125.956; 6.182; 19.745
90; 90.35; 90		3168Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029394 CIFC34 H34 O4P 1 21/n 115.8962; 23.9751; 15.4845
90; 115.677; 90		5318.6Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029395 CIFC36 H38 O8P c c n14.3696; 24.357; 8.882
90; 90; 90		3108.7Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029396 CIFC30 H26P 1 21/c 111.2069; 11.0239; 18.5291
90; 90.694; 90		2288.99Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029397 CIFC35 H40 Cl2 N2 O3P 1 21/c 113.809; 10.376; 21.761
90; 94.95; 90		3106.3Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029398 CIFC32 H32 O5P 1 21/c 118.9058; 9.7027; 16.0143
90; 114.597; 90		2671.05Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029399 CIFC34 H34P -112.3177; 14.2234; 16.6636
84.729; 73.553; 66.674		2570.47Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029400 CIFC32 H26 F6 O3P 1 21/c 110.7473; 24.594; 10.5723
90; 107.995; 90		2657.8Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029401 CIFC36 H38 O8P -110.0529; 12.8185; 13.4817
102.978; 111.583; 93.167		1555.9Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029402 CIFC30 H26 F2 O3P b c a20.42; 10.0168; 23.6874
90; 90; 90		4845.1Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029403 CIFC32 H26 F6 O3P 1 21/n 18.7765; 26.7134; 23.5585
90; 90; 90		5523.3Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029404 CIFC32 H30 O4P n a 2114.6805; 15.8549; 10.8348
90; 90; 90		2521.88Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029405 CIFC32 H30 O4P -110.2734; 15.6266; 16.2315
107.797; 90.011; 91.077		2480.59Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029406 CIFC32 H32 O5C 1 2/c 124.0553; 9.1097; 24.6742
90; 98.351; 90		5349.7Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029407 CIFC34 H34 O6P -110.3767; 12.3787; 21.9131
87.931; 84.966; 88.166		2800.88Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029408 CIFC34.5 H37 N O1.5P 1 n 110.9755; 11.2553; 22.7841
90; 94.201; 90		2807.02Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029409 CIFC30 H24 N2 O6C 1 2/c 121.8582; 11.2916; 20.2879
90; 99.753; 90		4935Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029410 CIFC32 H24 N2 O2P 1 21/c 19.5203; 23.024; 11.6499
90; 100.456; 90		2511.2Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029411 CIFC36 H38 O8P -16.867; 14.544; 15.106
83.765; 89.255; 89.174		1499.5Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029412 CIFC32 H32 O5P -18.0506; 13.1393; 13.3586
68.499; 76.048; 76.844		1260.68Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029413 CIFC34 H38 O6P 1 21/n 112.0322; 11.9498; 20.361
90; 100.039; 90		2882.73Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029414 CIFC34 H32 F6 N2 OP 1 2/c 123.741; 8.7785; 28.77
90; 103.418; 90		5832.3Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029415 CIFC32 H30P 1 21/c 110.3391; 22.1229; 10.9627
90; 110.352; 90		2350.97Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029416 CIFC34 H34 O6P 1 21/c 111.834; 21.682; 21.523
90; 94.25; 90		5507Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029417 CIFC32 H31 N OP 1 21/c 111.173; 25.204; 9.16
90; 102.144; 90		2522Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok
Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways.
The Journal of organic chemistry, 2014, 79, 4528-4543
4029418 CIFC33 H33 Cl2 N3 O3P 1 21 111.7883; 17.9576; 14.1225
90; 90.594; 90		2989.4Tan, Wei; Du, Bai-Xiang; Li, Xin; Zhu, Xu; Shi, Feng; Tu, Shu-Jiang
Catalytic Asymmetric Aza-ene Reaction of 3-Indolylmethanols with Cyclic Enaminones: Enantioselective Approach to C3-Functionalized Indoles.
The Journal of organic chemistry, 2014, 79, 4635-4643
4029419 CIFC31 H28 Cl N3 O2P 32 2 114.5913; 14.5913; 24.0429
90; 90; 120		4433.1Tan, Wei; Du, Bai-Xiang; Li, Xin; Zhu, Xu; Shi, Feng; Tu, Shu-Jiang
Catalytic Asymmetric Aza-ene Reaction of 3-Indolylmethanols with Cyclic Enaminones: Enantioselective Approach to C3-Functionalized Indoles.
The Journal of organic chemistry, 2014, 79, 4635-4643
4029420 CIFC14 H12 O2P 1 21/n 16.644; 10.4808; 15.2251
90; 100.429; 90		1042.68Thangaraj, Manikandan; Bhojgude, Sachin Suresh; Bisht, Rajesh H.; Gonnade, Rajesh G.; Biju, Akkattu T.
Diels-Alder Reaction of Tropones with Arynes: Synthesis of Functionalized Benzobicyclo[3.2.2]nonatrienones.
The Journal of organic chemistry, 2014, 79, 4757-4762
4029425 CIFC20 H29 I N O11P 1 21 19.1343; 6.8955; 20.2243
90; 91.191; 90		1273.56Islam, Maidul; Tirukoti, Nishanth D.; Nandi, Shyamapada; Hotha, Srinivas
Hypervalent iodine mediated synthesis of C-2 deoxy glycosides and amino Acid glycoconjugates.
The Journal of organic chemistry, 2014, 79, 4470-4476
4029426 CIFC20 H20 N2 O3P 1 21/c 110.12; 10.669; 16.642
90; 106.45; 90		1723.3En, Da; Zou, Gong-Feng; Guo, Yuan; Liao, Wei-Wei
Nucleophilic Phosphine-Catalyzed Intramolecular Michael Reactions of N-Allylic Substituted α-Amino Nitriles: Construction of Functionalized Pyrrolidine Rings via 5-endo-trig Cyclizations.
The Journal of organic chemistry, 2014, 79, 4456-4462
4029427 CIFC66 H132 Cl6 N12 O39P 1 21 113.685; 20.3904; 17.52
90; 105.773; 90		4704.7Faggi, Enrico; Moure, Alejandra; Bolte, Michael; Vicent, Cristian; Luis, Santiago V.; Alfonso, Ignacio
Pseudopeptidic cages as receptors for N-protected dipeptides.
The Journal of organic chemistry, 2014, 79, 4590-4601
4029428 CIFC25 H25 Br N4 O4C 1 2 141.527; 11.0922; 26.113
90; 123.323; 90		10051Li, Tian-Ze; Wang, Xi-Bo; Sha, Feng; Wu, Xin-Yan
Organocatalyzed enantioselective mannich reaction of pyrazoleamides with isatin-derived ketimines.
The Journal of organic chemistry, 2014, 79, 4332-4339
4029429 CIFC27 H20 N2 SeP 1 21/c 113.77; 9.3234; 17.015
90; 101.934; 90		2137.2Murai, Toshiaki; Yamaguchi, Kirara; Hori, Fumihiko; Maruyama, Toshifumi
Reaction of selenoamide dianions with thio- and selenoformamides leading to the formation of 5-aminoselenazoles: photophysical and electrochemical properties.
The Journal of organic chemistry, 2014, 79, 4930-4939
4029430 CIFC18 H18 N2P -19.0667; 9.4296; 9.8594
112.774; 98.136; 107.001		711.6Orejarena Pacheco, Julio Cesar; Opatz, Till
Ring Expansion of 1,2,3,4-Tetrahydroisoquinolines to Dibenzo[c,f]azonines. An Unexpected [1,4]-Sigmatropic Rearrangement of Nitrile-Stabilized Ammonium Ylides.
The Journal of organic chemistry, 2014, 79, 5182-5192
4029431 CIFC20 H22 N2 O2P 1 21/c 114.3891; 9.2391; 13.2215
90; 107.576; 90		1675.64Orejarena Pacheco, Julio Cesar; Opatz, Till
Ring Expansion of 1,2,3,4-Tetrahydroisoquinolines to Dibenzo[c,f]azonines. An Unexpected [1,4]-Sigmatropic Rearrangement of Nitrile-Stabilized Ammonium Ylides.
The Journal of organic chemistry, 2014, 79, 5182-5192
4029432 CIFC25 H29 N O6P 21 21 216.4802; 13.1979; 25.4488
90; 90; 90		2176.51Selfridge, Brandon R.; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.
Synthesis of Enantiopure 10-Nornaltrexones in the Search for Toll-like Receptor 4 Antagonists and Opioid Ligands.
The Journal of organic chemistry, 2014, 79, 5007-5018
4029433 CIFC18 H21 N O3P 21 21 215.8822; 15.7145; 16.2267
90; 90; 90		1499.93Selfridge, Brandon R.; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.
Synthesis of Enantiopure 10-Nornaltrexones in the Search for Toll-like Receptor 4 Antagonists and Opioid Ligands.
The Journal of organic chemistry, 2014, 79, 5007-5018
4029434 CIFC27 H23 N3 O4P 1 21/n 19.4852; 16.6744; 15.2017
90; 94.942; 90		2395.36Cui, Bao-Dong; Zuo, Jian; Zhao, Jian-Qiang; Zhou, Ming-Qiang; Wu, Zhi-Jun; Zhang, Xiao-Mei; Yuan, Wei-Cheng
Tandem Michael addition-ring transformation reactions of 3-hydroxyoxindoles/3-aminooxindoles with olefinic azlactones: direct access to structurally diverse spirocyclic oxindoles.
The Journal of organic chemistry, 2014, 79, 5305-5314
4029435 CIFC23 H18 N2 O4 SP 1 21/n 110.2604; 15.8897; 13.009
90; 108.475; 90		2011.61Cui, Bao-Dong; Zuo, Jian; Zhao, Jian-Qiang; Zhou, Ming-Qiang; Wu, Zhi-Jun; Zhang, Xiao-Mei; Yuan, Wei-Cheng
Tandem Michael addition-ring transformation reactions of 3-hydroxyoxindoles/3-aminooxindoles with olefinic azlactones: direct access to structurally diverse spirocyclic oxindoles.
The Journal of organic chemistry, 2014, 79, 5305-5314
4029436 CIFC32 H36 O8P 1 21/c 123.162; 11.5821; 11.2981
90; 100.997; 90		2975.2Vibhute, Amol M.; Sureshan, Kana M.
Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding.
The Journal of organic chemistry, 2014, 79, 4892-4908
4029437 CIFC25 H32 O7P 1 21/c 112.15; 10.181; 18.898
90; 95.579; 90		2326.6Vibhute, Amol M.; Sureshan, Kana M.
Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding.
The Journal of organic chemistry, 2014, 79, 4892-4908
4029438 CIFC36 H38 Cl2 O7P -112.0165; 16.3915; 18.4237
114.762; 103.433; 92.396		3165.08Vibhute, Amol M.; Sureshan, Kana M.
Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding.
The Journal of organic chemistry, 2014, 79, 4892-4908
4029439 CIFC28 H44 O8C 1 c 146.9596; 12.7191; 20.5382
90; 107.083; 90		11725.9Vibhute, Amol M.; Sureshan, Kana M.
Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding.
The Journal of organic chemistry, 2014, 79, 4892-4908
4029440 CIFC23 H36 O7P -117.077; 17.49; 17.638
102.333; 92.957; 117.285		4505.6Vibhute, Amol M.; Sureshan, Kana M.
Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding.
The Journal of organic chemistry, 2014, 79, 4892-4908
4029445 CIFC24 H18 O2P 21 21 216.993; 8.884; 26.801
90; 90; 90		1665Mori, Hiroki; Chen, Xi-Chao; Chang, Ning-Hui; Hamao, Shino; Kubozono, Yoshihiro; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of methoxy-substituted picenes: substitution position effect on their electronic and single-crystal structures.
The Journal of organic chemistry, 2014, 79, 4973-4983
4029446 CIFC24 H18 O2P 21 21 216.2114; 7.8271; 34.589
90; 90; 90		1681.6Mori, Hiroki; Chen, Xi-Chao; Chang, Ning-Hui; Hamao, Shino; Kubozono, Yoshihiro; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of methoxy-substituted picenes: substitution position effect on their electronic and single-crystal structures.
The Journal of organic chemistry, 2014, 79, 4973-4983
4029447 CIFC26 H22 O4P 1 21/n 17.043; 19.934; 13.754
90; 90.379; 90		1931Mori, Hiroki; Chen, Xi-Chao; Chang, Ning-Hui; Hamao, Shino; Kubozono, Yoshihiro; Nakajima, Kiyohiko; Nishihara, Yasushi
Synthesis of methoxy-substituted picenes: substitution position effect on their electronic and single-crystal structures.
The Journal of organic chemistry, 2014, 79, 4973-4983
4029448 CIFC18 H15 F3 N2 O2 SP 1 21/n 112.393; 10.745; 13.09
90; 100.07; 90		1716.2Wang, Nuancheng; Li, Renhe; Li, Liubo; Xu, Shansheng; Song, Haibin; Wang, Baiquan
Rhodium(III)-Catalyzed Intermolecular Amidation with Azides via C(sp(3))-H Functionalization.
The Journal of organic chemistry, 2014, 79, 5379-5385
4029449 CIFC21 H25 N O3P 21 21 2110.1714; 10.7715; 16.287
90; 90; 90		1784.4Curto, John M.; Kozlowski, Marisa C.
α-Allyl-α-aryl α-Amino Esters in the Asymmetric Synthesis of Acyclic and Cyclic Amino Acid Derivatives by Alkene Metathesis.
The Journal of organic chemistry, 2014, 79, 5359-5364
4029450 CIFC23 H28 F3 N O7P 21 21 218.9709; 14.6155; 18.1662
90; 90; 90		2381.8Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko
Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium.
The Journal of organic chemistry, 2014, 79, 5287-5300
4029451 CIFC14 H23 N O5P 1 21 17.321; 11.808; 9.419
90; 110.277; 90		763.8Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko
Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium.
The Journal of organic chemistry, 2014, 79, 5287-5300
4029452 CIFC24 H38 N2 O7P 21 21 216.598; 11.093; 13.208
90; 90; 90		2431.9Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko
Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium.
The Journal of organic chemistry, 2014, 79, 5287-5300
4029453 CIFC24 H38 N2 O7P 21 21 211.046; 16.939; 13.237
90; 90; 90		2476.8Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko
Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium.
The Journal of organic chemistry, 2014, 79, 5287-5300
4029454 CIFC25 H34 N2 O7 SP 21 21 219.909; 12.774; 19.563
90; 90; 90		2476.2Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko
Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium.
The Journal of organic chemistry, 2014, 79, 5287-5300
4029455 CIFC34 H48 Br N3 O10P 21 21 2110.0129; 17.402; 20.03
90; 90; 90		3490.1Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko
Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium.
The Journal of organic chemistry, 2014, 79, 5287-5300
4029456 CIFC19 H21 Cl N4 OP 1 21/n 17.583; 8.075; 28.833
90; 95.49; 90		1757.4Martinez-Ariza, Guillermo; Ayaz, Muhammad; Medda, Federico; Hulme, Christopher
Synthesis of diverse nitrogen-enriched heterocyclic scaffolds using a suite of tunable one-pot multicomponent reactions.
The Journal of organic chemistry, 2014, 79, 5153-5162
4029457 CIFC18 H18 F N5 O3C 1 2/c 121.4045; 9.0833; 17.5993
90; 94.482; 90		3411.3Martinez-Ariza, Guillermo; Ayaz, Muhammad; Medda, Federico; Hulme, Christopher
Synthesis of diverse nitrogen-enriched heterocyclic scaffolds using a suite of tunable one-pot multicomponent reactions.
The Journal of organic chemistry, 2014, 79, 5153-5162
4029458 CIFC14 H15 Br Cl N3 O3P -18.9862; 9.873; 10.3897
115.309; 100.343; 104.653		761.34Martinez-Ariza, Guillermo; Ayaz, Muhammad; Medda, Federico; Hulme, Christopher
Synthesis of diverse nitrogen-enriched heterocyclic scaffolds using a suite of tunable one-pot multicomponent reactions.
The Journal of organic chemistry, 2014, 79, 5153-5162
4029459 CIFC18 H17 Cl O3P 21 21 214.878; 16.418; 19.847
90; 90; 90		1589.5Zeng, Zhongyi; Yang, Dingqiao; Long, Yuhua; Pan, Xuejing; Huang, Guobao; Zuo, Xiongjun; Zhou, Wen
Nickel-catalyzed asymmetric ring opening of oxabenzonorbornadienes with arylboronic acids.
The Journal of organic chemistry, 2014, 79, 5249-5257
4029460 CIFC12 H19 N O4P -111.119; 11.175; 18.547
77.91; 84.55; 60.74		1966Zhou, Lili; Yao, Yanmin; Xu, Wenbo; Liang, Guangxin
Total Syntheses of (±)-Omphadiol and (±)-Pyxidatol C through a Cis-Fused 5,7-Carbocyclic Common Intermediate.
The Journal of organic chemistry, 2014, 79, 5345-5350
4029461 CIFC14 H19 Cl2 O PP 1 21 16.547; 14.435; 7.735
90; 108.659; 90		692.6Fokin, Andrey A.; Yurchenko, Raisa I.; Tkachenko, Boryslav A.; Fokina, Natalie A.; Gunawan, Maria A.; Poinsot, Didier; Dahl, Jeremy E. P.; Carlson, Robert M. K.; Serafin, Michael; Cattey, Hélène; Hierso, Jean-Cyrille; Schreiner, Peter R.
Selective preparation of diamondoid phosphonates.
The Journal of organic chemistry, 2014, 79, 5369-5373
4029462 CIFC26 H31 Cl2 O PP 1 21/m 18.5927; 12.5125; 9.8811
90; 107.977; 90		1010.5Fokin, Andrey A.; Yurchenko, Raisa I.; Tkachenko, Boryslav A.; Fokina, Natalie A.; Gunawan, Maria A.; Poinsot, Didier; Dahl, Jeremy E. P.; Carlson, Robert M. K.; Serafin, Michael; Cattey, Hélène; Hierso, Jean-Cyrille; Schreiner, Peter R.
Selective preparation of diamondoid phosphonates.
The Journal of organic chemistry, 2014, 79, 5369-5373
4029463 CIFC22 H27 Cl2 O PP 1 21/n 113.7657; 6.5028; 20.58
90; 91.615; 90		1841.5Fokin, Andrey A.; Yurchenko, Raisa I.; Tkachenko, Boryslav A.; Fokina, Natalie A.; Gunawan, Maria A.; Poinsot, Didier; Dahl, Jeremy E. P.; Carlson, Robert M. K.; Serafin, Michael; Cattey, Hélène; Hierso, Jean-Cyrille; Schreiner, Peter R.
Selective preparation of diamondoid phosphonates.
The Journal of organic chemistry, 2014, 79, 5369-5373
4029464 CIFC18 H26 N2 O5 S SiP 1 21 17.1772; 7.3897; 20.5531
90; 91.23; 90		1089.83Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029465 CIFC17 H20 N2 O5 SP 21 21 216.1282; 8.0712; 36.366
90; 90; 90		1798.7Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029466 CIFC19 H28 N2 O5 S SiP 1 21 17.2155; 7.3686; 21.8244
90; 91.207; 90		1160.11Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029467 CIFC11 H15 N O2 SP 1 21/n 112.4009; 7.2781; 12.4672
90; 94.562; 90		1121.66Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029468 CIFC22 H31 Co2 N O9 S SiP 21 21 2112.5959; 12.7985; 18.2292
90; 90; 90		2938.7Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029469 CIFC12 H12 N2 O4 SP 1 21 17.7299; 8.0026; 21.4995
90; 91.981; 90		1329.15Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029470 CIFC16 H16 N2 O4 SP 1 21 17.6048; 7.3949; 13.9958
90; 94.525; 90		784.62Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029471 CIFC11 H14 N2 O4 SP 1 21 17.3131; 12.6022; 28.2003
90; 95.198; 90		2588.28Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029472 CIFC19 H28 N2 O5 S SiP 1 21 19.956; 7.927; 14.0034
90; 96.822; 90		1097.34Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M
Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions.
The Journal of organic chemistry, 2014, 79, 5121-5133
4029474 CIFC29 H26 N6P 1 21/n 19.5645; 15.6682; 17.0313
90; 95.23; 90		2541.7Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen
Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles.
The Journal of organic chemistry, 2014, 79, 5258-5268
4029475 CIFC28 H22 Br2 N4 OP 1 21/c 118.4011; 6.1969; 23.223
90; 105.394; 90		2553.1Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen
Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles.
The Journal of organic chemistry, 2014, 79, 5258-5268
4029476 CIFC26 H20 Cl2 N6P 1 21/n 19.585; 12.7985; 18.4861
90; 91.299; 90		2267.2Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen
Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles.
The Journal of organic chemistry, 2014, 79, 5258-5268
4029477 CIFC36 H30 N6 O2C 1 2/c 132.018; 9.2309; 21.6503
90; 110.711; 90		5985.3Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen
Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles.
The Journal of organic chemistry, 2014, 79, 5258-5268
4029478 CIFC47 H55 Cl3 N8 O8C 1 2/c 147.727; 14.35; 17.94
90; 102.5; 90		11996Shang, Jie; Gallagher, Nolan M.; Bie, Fusheng; Li, Qiaolian; Che, Yanke; Wang, Ying; Jiang, Hua
Aromatic triazole foldamers induced by C-h···x (x = f, cl) intramolecular hydrogen bonding.
The Journal of organic chemistry, 2014, 79, 5134-5144
4029479 CIFC37 H37 F3 N6 O6P 1 21/c 19.6484; 13.075; 28.303
90; 98.2; 90		3534Shang, Jie; Gallagher, Nolan M.; Bie, Fusheng; Li, Qiaolian; Che, Yanke; Wang, Ying; Jiang, Hua
Aromatic triazole foldamers induced by C-h···x (x = f, cl) intramolecular hydrogen bonding.
The Journal of organic chemistry, 2014, 79, 5134-5144
4029480 CIFC55 H103 N18 O11P 1 21 110.379; 33.918; 19.627
90; 99.06; 90		6823Fremaux, Juliette; Kauffmann, Brice; Guichard, Gilles
Synthesis and folding propensity of aliphatic oligoureas containing repeats of proline-type units.
The Journal of organic chemistry, 2014, 79, 5494-5502
4029481 CIFC58 H111 N19 O11C 1 2 118.609; 20; 21.577
90; 107.06; 90		7677Fremaux, Juliette; Kauffmann, Brice; Guichard, Gilles
Synthesis and folding propensity of aliphatic oligoureas containing repeats of proline-type units.
The Journal of organic chemistry, 2014, 79, 5494-5502
4029482 CIFC20 H37 B2 N3 O5P 21 21 2110.4871; 11.1272; 19.6809
90; 90; 90		2296.6Müller, Matthias; Maichle-Mössmer, Cäcilia; Bettinger, Holger F.
Boryl azides in 1,3-dipolar cycloadditions.
The Journal of organic chemistry, 2014, 79, 5478-5483
4029483 CIFC8 H15 N3 OP 1 21/n 17.2695; 15.2273; 8.6831
90; 107.665; 90		915.9Müller, Matthias; Maichle-Mössmer, Cäcilia; Bettinger, Holger F.
Boryl azides in 1,3-dipolar cycloadditions.
The Journal of organic chemistry, 2014, 79, 5478-5483
4029504 CIFC24 H16 Cl4 N4P 1 21/c 117.0237; 9.7682; 14.0662
90; 93.164; 90		2335.52Parent, Alexander A.; Ess, Daniel H.; Katzenellenbogen, John A.
π-π Interaction Energies as Determinants of the Photodimerization of Mono-, Di-, and Triazastilbenes.
The Journal of organic chemistry, 2014, 79, 5448-5462
4029505 CIFC13 H10 Cl2 N2 OP 1 21/c 14.164; 26.744; 11.3686
90; 92.945; 90		1264.36Parent, Alexander A.; Ess, Daniel H.; Katzenellenbogen, John A.
π-π Interaction Energies as Determinants of the Photodimerization of Mono-, Di-, and Triazastilbenes.
The Journal of organic chemistry, 2014, 79, 5448-5462
4029506 CIFC12 H8 Cl2 N2P -17.3168; 10.967; 14.476
87.087; 77.914; 79.985		1118.4Parent, Alexander A.; Ess, Daniel H.; Katzenellenbogen, John A.
π-π Interaction Energies as Determinants of the Photodimerization of Mono-, Di-, and Triazastilbenes.
The Journal of organic chemistry, 2014, 79, 5448-5462
4029507 CIFC12 H8 Cl2 N2P 1 21/n 113.6016; 5.1312; 16.377
90; 94.686; 90		1139.17Parent, Alexander A.; Ess, Daniel H.; Katzenellenbogen, John A.
π-π Interaction Energies as Determinants of the Photodimerization of Mono-, Di-, and Triazastilbenes.
The Journal of organic chemistry, 2014, 79, 5448-5462
4029508 CIFC25 H22 N2 O6 SP -110.1565; 10.4149; 11.8711
96.047; 110.545; 105.94		1101.9French, Jonathan M.; Diver, Steven T.
Gold(I)-Promoted Heterocyclization of Internal Alkynes: A Comparative Study of Direct Metallate 5-endo-dig Cyclization versus a Stepwise Cyclization.
The Journal of organic chemistry, 2014, 79, 5569-5585
4029509 CIFC18 H18 N2 O2P -19.088; 12.184; 15.086
101.612; 90.49; 107.47		1556.5Coyle, Robert; McArdle, Patrick; Aldabbagh, Fawaz
Tandem Reactions via Barton Esters with Intermolecular Addition and Vinyl Radical Substitution onto Indole.
The Journal of organic chemistry, 2014, 79, 5903-5907
4029510 CIFC22 H18 N2 O2P -19.2424; 10.0425; 11.6734
66.357; 76.443; 63.89		889Coyle, Robert; McArdle, Patrick; Aldabbagh, Fawaz
Tandem Reactions via Barton Esters with Intermolecular Addition and Vinyl Radical Substitution onto Indole.
The Journal of organic chemistry, 2014, 79, 5903-5907
4029511 CIFC19 H28 O4P 1 21 17.2917; 12.21; 9.926
90; 107.842; 90		841.2Mydock-McGrane, Laurel; Rath, Nigam P.; Covey, Douglas F.
Synthesis of a Smoothened Cholesterol: 18,19-Di-nor-cholesterol.
The Journal of organic chemistry, 2014, 79, 5636-5643
4029512 CIFC24 H40 O3I 1 2 115.9947; 6.2325; 21.7799
90; 99.498; 90		2141.41Mydock-McGrane, Laurel; Rath, Nigam P.; Covey, Douglas F.
Synthesis of a Smoothened Cholesterol: 18,19-Di-nor-cholesterol.
The Journal of organic chemistry, 2014, 79, 5636-5643
4029513 CIFC96 H140 N6 O10P 21 21 2113.9132; 17.1884; 38.339
90; 90; 90		9168.6Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029514 CIFC120 H138 N14 O24P 1 n 122.564; 21.265; 23.331
90; 90.599; 90		11194.1Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029515 CIFC144 H160.5 Cl6 N17.5 O11P 1 21/n 118.841; 33.095; 21.482
90; 95.513; 90		13333Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029516 CIFC140.75 H156.75 Cl5.25 N15 O9P 1 21/n 118.928; 33.493; 20.956
90; 94.462; 90		13245Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029517 CIFC127.85 H148.7 Cl3.45 N15.85 O25P -117.391; 18.813; 21.08
75.75; 80.301; 64.164		6001.7Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029518 CIFC144 H160 Cl6 N16 O10P -116.6712; 19.0842; 20.6478
87.705; 83.78; 87.876		6521.8Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029519 CIFC129.75 H148 Cl3.75 N14.25 O8P -116.5188; 17.8039; 21.7829
95.035; 105.878; 102.007		5955.4Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029520 CIFC134.75 H149.5 Cl6.75 N15.75 O9P 1 21/n 116.893; 33.201; 22.7244
90; 105.709; 90		12269.3Galán, Albano; Escudero-Adán, Eduardo C; Frontera, Antonio; Ballester, Pablo
Synthesis, Structure, and Binding Properties of Lipophilic Cavitands Based on a Calix[4]pyrrole-Resorcinarene Hybrid Scaffold.
The Journal of organic chemistry, 2014, 79, 5545-5557
4029521 CIFC18 H22 N2 O2 SP 21 21 217.84822; 8.2682; 26.3414
90; 90; 90		1709.31Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029522 CIFC11 H14 N2 O3 SP -17.90888; 8.8674; 9.2796
83.012; 69.9059; 75.1847		590.45Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029523 CIFC18 H20 N2 O3 SP 21 21 216.53799; 13.6252; 18.5986
90; 90; 90		1656.79Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029524 CIFC12 H16 N2 O3 SP 21 21 216.55092; 8.59104; 23.0273
90; 90; 90		1295.96Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029525 CIFC18 H22 N2 O2 SP 21 21 217.8482; 8.2717; 26.3382
90; 90; 90		1709.82Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029526 CIFC12 H18 N2 O2 SP 21 21 219.19794; 10.68037; 12.7106
90; 90; 90		1248.66Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029527 CIFC17 H20 N2 O2 SP -17.709; 8.0411; 13.5247
80.1484; 89.0366; 76.3943		802.6Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029528 CIFC12 H18 N2 O2 SP 21 21 219.1971; 10.6801; 12.7121
90; 90; 90		1248.66Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029529 CIFC11 H16 N2 O2 SP -17.9146; 8.8541; 9.1732
104.507; 95.7341; 110.408		570.71Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029530 CIFC12 H16 N2 O3 SP 1 21/c 17.53664; 24.0628; 7.45283
90; 111.955; 90		1253.57Yoneda, Tetsuya; Tabata, Hidetsugu; Nakagomi, Jun; Tasaka, Tomohiko; Oshitari, Tetsuta; Takahashi, Hideyo; Natsugari, Hideaki
N-Benzoyl- and N-Sulfonyl-1,5-benzodiazepines: Comparison of Their Atropisomeric and Conformational Properties.
The Journal of organic chemistry, 2014, 79, 5717-5727
4029531 CIFC14 H10 F N O SP -17.124; 7.495; 11.828
96.72; 100.31; 108.79		578Cheng, Yannan; Peng, Qian; Fan, Weigang; Li, Pixu
Room-temperature ligand-free pd/c-catalyzed C-s bond formation: synthesis of 2-substituted benzothiazoles.
The Journal of organic chemistry, 2014, 79, 5812-5819
4029532 CIFC20 H17 F3 O2P 21 21 27.5685; 28.8622; 8.1132
90; 90; 90		1772.28Cai, Hua; Nie, Jing; Zheng, Yan; Ma, Jun-An
Lithium binaphtholate-catalyzed enantioselective enyne addition to ketones: access to enynylated tertiary alcohols.
The Journal of organic chemistry, 2014, 79, 5484-5493
4029533 CIFC22 H20 O2P 21 21 218.351; 11.258; 18.802
90; 90; 90		1768Cai, Hua; Nie, Jing; Zheng, Yan; Ma, Jun-An
Lithium binaphtholate-catalyzed enantioselective enyne addition to ketones: access to enynylated tertiary alcohols.
The Journal of organic chemistry, 2014, 79, 5484-5493
4029587 CIFC11 H12 Cl N3 OP -128.311; 10.0361; 8.1588
90; 90; 90		2318.2Mishra, Kunj B.; Tiwari, Vinod K.
Click chemistry inspired synthesis of morpholine-fused triazoles.
The Journal of organic chemistry, 2014, 79, 5752-5762
4029588 CIFC14 H14 N6 OP 1 c 110.7516; 5.7473; 11.2884
90; 104.7; 90		674.71Mishra, Kunj B.; Tiwari, Vinod K.
Click chemistry inspired synthesis of morpholine-fused triazoles.
The Journal of organic chemistry, 2014, 79, 5752-5762
4029589 CIFC18 H26 N6 O6P 1 21 116.973; 6.849; 18.923
90; 105.83; 90		2116.3Mishra, Kunj B.; Tiwari, Vinod K.
Click chemistry inspired synthesis of morpholine-fused triazoles.
The Journal of organic chemistry, 2014, 79, 5752-5762
4029590 CIFC14 H20 N6 O2P 1 21/c 110.6543; 14.9406; 9.9564
90; 104.191; 90		1536.5Mishra, Kunj B.; Tiwari, Vinod K.
Click chemistry inspired synthesis of morpholine-fused triazoles.
The Journal of organic chemistry, 2014, 79, 5752-5762
4029591 CIFC31 H56 O5P 1 21 112.754; 6.03911; 19.9264
90; 95.38; 90		1528.03Hirayama, Yui; Okuzumi, Keiko; Masubuti, Hironori; Uekusa, Hidehiro; Girault, Jean-Pierre; Fujimoto, Yoshinori
Stereochemical Assignment of C-24 and C-25 of Amarasterone A, a Putative Biosynthetic Intermediate of Cyasterone.
The Journal of organic chemistry, 2014, 79, 5471-5477
4029592 CIFC30 H50 O3C 1 2 129.1632; 6.6782; 14.5294
90; 98.666; 90		2797.4Hirayama, Yui; Okuzumi, Keiko; Masubuti, Hironori; Uekusa, Hidehiro; Girault, Jean-Pierre; Fujimoto, Yoshinori
Stereochemical Assignment of C-24 and C-25 of Amarasterone A, a Putative Biosynthetic Intermediate of Cyasterone.
The Journal of organic chemistry, 2014, 79, 5471-5477
4029593 CIFC79 H31 Cl2 F5 O9P b c a14.9459; 19.7129; 36.9458
90; 90; 90		10885.2Liang, Sisi; Xu, Liang; Jia, Zhenshan; Gan, Liangbing
Pentafluorophenyl Transfer Reaction: Preparation of Pentafluorophenyl [60]Fullerene Adducts through Opening of Fullerene Epoxide Moiety with Trispentafluorophenylborane.
The Journal of organic chemistry, 2014, 79, 5794-5798
4029594 CIFC26 Br N2 O3P 41 21 212.1532; 12.1532; 35.5177
90; 90; 90		5245.97Reeves, Jonathan T.; Lorenc, Chris; Camara, Kaddy; Li, Zhibin; Lee, Heewon; Busacca, Carl A.; Senanayake, Chris H.
Carbamoyl anion addition to nitrones.
The Journal of organic chemistry, 2014, 79, 5895-5902
4029595 CIFC16 H13 N2 O4P 21 21 215.9579; 8.2268; 29.991
90; 90; 90		1469.99Dev, Dharm; Palakurthy, Nani Babu; Thalluri, Kishore; Chandra, Jyoti; Mandal, Bhubaneswar
Ethyl 2-Cyano-2-(2-nitrobenzenesulfonyloxyimino)acetate (o-NosylOXY): A Recyclable Coupling Reagent for Racemization-Free Synthesis of Peptide, Amide, Hydroxamate, and Ester.
The Journal of organic chemistry, 2014, 79, 5420-5431
4029600 CIFC40 H32 N2 O8 SP 1 21 110.603; 14.746; 10.89
90; 92.786; 90		1700.7Mitra, Tapobrata; Jana, Saibal; Pandey, Sharmila; Bhattacharya, Prabuddha; Khamrai, Uttam K.; Anoop, Anakuthil; Basak, Amit
Asymmetric garratt-braverman cyclization: a route to axially chiral aryl naphthalene-amino Acid hybrids.
The Journal of organic chemistry, 2014, 79, 5608-5616
4029601 CIFC22 H18 O6 SP -18.8819; 13.355; 16.688
102.679; 97.844; 90.512		1911.6Mitra, Tapobrata; Jana, Saibal; Pandey, Sharmila; Bhattacharya, Prabuddha; Khamrai, Uttam K.; Anoop, Anakuthil; Basak, Amit
Asymmetric garratt-braverman cyclization: a route to axially chiral aryl naphthalene-amino Acid hybrids.
The Journal of organic chemistry, 2014, 79, 5608-5616
4029602 CIFC42 H48 Cu F6 N4 PC 1 2/c 132.815; 11.058; 25.545
90; 124.773; 90		7614Tran, Anh T.; Liu, Peng; Houk, K. N.; Nicholas, Kenneth M.
Regioselectivity in the cu(i)-catalyzed [4 + 2]-cycloaddition of 2-nitrosopyridine with unsymmetrical dienes.
The Journal of organic chemistry, 2014, 79, 5617-5626
4029603 CIFC14 H9 N3F d d 210.7584; 41.2284; 9.1427
90; 90; 90		4055.26Li, Chao; Zhang, Wen-Ting; Wang, Xiang-Shan
CuI-Catalyzed C-N Bond Formation and Cleavage for the Synthesis of Benzimidazo[1,2-a]quinazoline Derivatives.
The Journal of organic chemistry, 2014, 79, 5847-5851
4029604 CIFC15 H11 I O2P 1 21 19.8867; 5.6677; 11.9084
90; 98.44; 90		660.06Kong, Wei; Che, Chao; Wu, Jialin; Ma, Liai; Zhu, Gangguo
Pd-Catalyzed Regio- and Stereoselective Addition of Boronic Acids to Silylacetylenes: A Stereodivergent Assembly of β,β-Disubstituted Alkenylsilanes and Alkenyl Halides.
The Journal of organic chemistry, 2014, 79, 5799-5805
4029605 CIFC13 H20 O4C 1 2 19.981; 8.448; 15.97
90; 103.21; 90		1311Ishihara, Jun; Tsuru, Hiroaki; Hatakeyama, Susumi
Total synthesis of (-)-dihydrosporothriolide utilizing an indium-mediated reformatsky-claisen rearrangement.
The Journal of organic chemistry, 2014, 79, 5908-5913
4029606 CIFC19 H21 N3 O4C 1 c 110.8805; 17.9631; 10.2119
90; 110.147; 90		1873.77Janody, Simon; Hermange, Philippe; Retailleau, Pascal; Thierry, Josiane; Dodd, Robert H.
Diastereoselective Three-Component Vinylogous Mannich Reaction of Nitrogen Heterocycles, Acyl/Sulfonyl Chlorides, and Silyloxyfurans/pyrroles.
The Journal of organic chemistry, 2014, 79, 5673-5683
4029607 CIFC14 H12 N2 O3P 1 21/c 18.1942; 14.4078; 10.1791
90; 96.39; 90		1194.28Janody, Simon; Hermange, Philippe; Retailleau, Pascal; Thierry, Josiane; Dodd, Robert H.
Diastereoselective Three-Component Vinylogous Mannich Reaction of Nitrogen Heterocycles, Acyl/Sulfonyl Chlorides, and Silyloxyfurans/pyrroles.
The Journal of organic chemistry, 2014, 79, 5673-5683
4029608 CIFC19 H15 N O3P c a 2112.0964; 12.2829; 10.317
90; 90; 90		1532.89Janody, Simon; Hermange, Philippe; Retailleau, Pascal; Thierry, Josiane; Dodd, Robert H.
Diastereoselective Three-Component Vinylogous Mannich Reaction of Nitrogen Heterocycles, Acyl/Sulfonyl Chlorides, and Silyloxyfurans/pyrroles.
The Journal of organic chemistry, 2014, 79, 5673-5683
4029609 CIFC25 H24 Cl3 D N2 O4C 1 2/c 132.2117; 9.1944; 23.1388
90; 132.2; 90		5076.7Janody, Simon; Hermange, Philippe; Retailleau, Pascal; Thierry, Josiane; Dodd, Robert H.
Diastereoselective Three-Component Vinylogous Mannich Reaction of Nitrogen Heterocycles, Acyl/Sulfonyl Chlorides, and Silyloxyfurans/pyrroles.
The Journal of organic chemistry, 2014, 79, 5673-5683
4029610 CIFC22 H26 N2 O6P b c a11.2819; 16.3676; 23.2672
90; 90; 90		4296.5Janody, Simon; Hermange, Philippe; Retailleau, Pascal; Thierry, Josiane; Dodd, Robert H.
Diastereoselective Three-Component Vinylogous Mannich Reaction of Nitrogen Heterocycles, Acyl/Sulfonyl Chlorides, and Silyloxyfurans/pyrroles.
The Journal of organic chemistry, 2014, 79, 5673-5683
4029611 CIFC19 H15 N O4P 1 21/c 19.6682; 7.7791; 21.5345
90; 98.014; 90		1603.79Janody, Simon; Hermange, Philippe; Retailleau, Pascal; Thierry, Josiane; Dodd, Robert H.
Diastereoselective Three-Component Vinylogous Mannich Reaction of Nitrogen Heterocycles, Acyl/Sulfonyl Chlorides, and Silyloxyfurans/pyrroles.
The Journal of organic chemistry, 2014, 79, 5673-5683
4029612 CIFC40 H17 F15 N4P 21 21 219.5063; 15.9513; 26.92
90; 90; 90		4082.1Bruce, Alexandra M.; Weyburne, Emily S.; Engle, James T.; Ziegler, Christopher J.; Geier, 3rd, G Richard
Phlorins Bearing Different Substituents at the sp(3)-Hybridized Meso-Position.
The Journal of organic chemistry, 2014, 79, 5664-5672
4029613 CIFC55 H26 F15 N5P -18.3212; 14.29; 24.645
103.203; 95.918; 103.877		2730.9Bruce, Alexandra M.; Weyburne, Emily S.; Engle, James T.; Ziegler, Christopher J.; Geier, 3rd, G Richard
Phlorins Bearing Different Substituents at the sp(3)-Hybridized Meso-Position.
The Journal of organic chemistry, 2014, 79, 5664-5672
4029614 CIFC45 H19 F15 N4C 1 2/c 127.4367; 8.4546; 43.997
90; 96.863; 90		10132.7Bruce, Alexandra M.; Weyburne, Emily S.; Engle, James T.; Ziegler, Christopher J.; Geier, 3rd, G Richard
Phlorins Bearing Different Substituents at the sp(3)-Hybridized Meso-Position.
The Journal of organic chemistry, 2014, 79, 5664-5672
4029615 CIFC20 H17 N O4C 1 2/c 111.832; 19.09; 15.757
90; 100.83; 90		3495.7Zhou, Nini; Xie, Tao; Liu, Lin; Xie, Zhixiang
Cu/Mn Co-oxidized Cyclization for the Synthesis of Highly Substituted Pyrrole Derivatives from Amino Acid Esters: A Strategy for the Biomimetic Syntheses of Lycogarubin C and Chromopyrrolic Acid.
The Journal of organic chemistry, 2014, 79, 6061-6068
4029616 CIFC11 H12 N4 O2 SP 1 21/c 119.3293; 4.6077; 14.1682
90; 110.229; 90		1184.04Dürüst, Yaşar; Sağırlı, Akın
Microwave-Assisted Coupling Reaction of N-Aryl Sydnones with 2-Nitromethylenethiazolidine: Unexpected Formation of (Z)-2-(Nitro((E)-p-substitutedphenyldiazenyl)methylene)thiazolidines.
The Journal of organic chemistry, 2014, 79, 6380-6384
4029617 CIFC9 H10 O3P 1 21/c 19.1941; 6.6988; 13.353
90; 98.298; 90		813.8Bayir, Ali; Brewer, Matthias
Fragmentation of Bicyclic γ-Silyloxy-β-hydroxy-α-diazolactones as an Approach to Ynolides.
The Journal of organic chemistry, 2014, 79, 6037-6046
4029618 CIFC29 H22 O3P 1 21/c 113.084; 11.765; 14.203
90; 105.26; 90		2109.2Zhu, Shifa; Huang, Hua; Zhang, Zhicai; Ma, Tongmei; Jiang, Huanfeng
Mechanistic insight into transition metal-catalyzed reaction of enynal/enynone with alkenes: metal-dependent reaction pathway.
The Journal of organic chemistry, 2014, 79, 6113-6122
4029623 CIFC48 H38 Cl4 O8P 1 21/n 15.6255; 16.167; 23.905
90; 93; 90		2171.1Alcaide, Benito; Almendros, Pedro; Quirós, M Teresa; Lázaro, Carlos; Torres, M. Rosario
Three-Step Metal-Promoted Allene-Based Preparation of Bis(heterocyclic) Cyclophanes from Carbonyl Compounds.
The Journal of organic chemistry, 2014, 79, 6244-6255
4029624 CIFC34 H40 N2 O8P 21 21 218.6543; 12.7816; 29.198
90; 90; 90		3229.8Alcaide, Benito; Almendros, Pedro; Quirós, M Teresa; Lázaro, Carlos; Torres, M. Rosario
Three-Step Metal-Promoted Allene-Based Preparation of Bis(heterocyclic) Cyclophanes from Carbonyl Compounds.
The Journal of organic chemistry, 2014, 79, 6244-6255
4029625 CIFC16 H15 F O3 SP 1 21/c 19.4436; 9.3132; 17.109
90; 93.774; 90		1501.5Wang, Wengui; Shen, Haiming; Wan, Xiao-Long; Chen, Qing-Yun; Guo, Yong
Enantioselective Pd-Catalyzed Allylation of Acyclic α-Fluorinated Ketones.
The Journal of organic chemistry, 2014, 79, 6347-6353
4029626 CIFC28 H34 N2 O7 S2P -18.9439; 11.99; 14.673
107.716; 96.599; 100.669		1448.1Beiginejad, Hadi; Nematollahi, Davood
Electrochemical synthesis of sulfonamide derivatives based on the oxidation of 2,5-diethoxy-4-morpholinoaniline in the presence of arylsulfinic acids.
The Journal of organic chemistry, 2014, 79, 6326-6329
4029627 CIFC23 H29 N5 O7P 21 21 216.3618; 14.8963; 26.543
90; 90; 90		2515.4Milli, Lorenzo; Larocca, Michele; Tedesco, Mattia; Castellucci, Nicola; Ghibaudi, Elena; Cornia, Andrea; Calvaresi, Matteo; Zerbetto, Francesco; Tomasini, Claudia
α,ε-Hybrid Foldamers with 1,2,3-Triazole Rings: Order versus Disorder.
The Journal of organic chemistry, 2014, 79, 5958-5969
4029628 CIFC37 H45 N10 O11P 1 21 111.3992; 9.8228; 19.0001
90; 94.297; 90		2121.5Milli, Lorenzo; Larocca, Michele; Tedesco, Mattia; Castellucci, Nicola; Ghibaudi, Elena; Cornia, Andrea; Calvaresi, Matteo; Zerbetto, Francesco; Tomasini, Claudia
α,ε-Hybrid Foldamers with 1,2,3-Triazole Rings: Order versus Disorder.
The Journal of organic chemistry, 2014, 79, 5958-5969
4029629 CIFC14 H23 Br N4 OP -18.7493; 9.6705; 10.0013
81.549; 65.834; 75.133		745.36Semakin, Artem N.; Sukhorukov, Alexey Yu; Nelyubina, Yulia V.; Khomutova, Yulia A.; Ioffe, Sema L.; Tartakovsky, Vladimir A.
Urotropine isomer (1,4,6,10-tetraazaadamantane): synthesis, structure, and chemistry.
The Journal of organic chemistry, 2014, 79, 6079-6086
4029630 CIFC19 H18 Cl2 N4 S ZnP 1 21/c 111.10561; 12.50496; 14.4266
90; 97.9938; 90		1984.03Vonlanthen, Mireille; Connelly, Colleen M.; Deiters, Alexander; Linden, Anthony; Finney, Nathaniel S.
Thiourea-based fluorescent chemosensors for aqueous metal ion detection and cellular imaging.
The Journal of organic chemistry, 2014, 79, 6054-6060
4029631 CIFC24 H11 Br F4 O2P 1 21/c 15.2823; 43.495; 9.5276
90; 119.975; 90		1896.2Widner, Danielle L.; Knauf, Qianwei R.; Merucci, Mark T.; Fritz, Thomas R.; Sauer, Jon S.; Speetzen, Erin D.; Bosch, Eric; Bowling, Nathan P.
Intramolecular halogen bonding supported by an aryldiyne linker.
The Journal of organic chemistry, 2014, 79, 6269-6278
4029632 CIFC25 H14 Br F3 O2P 1 21/c 19.8898; 26.9161; 7.5176
90; 97.266; 90		1985.1Widner, Danielle L.; Knauf, Qianwei R.; Merucci, Mark T.; Fritz, Thomas R.; Sauer, Jon S.; Speetzen, Erin D.; Bosch, Eric; Bowling, Nathan P.
Intramolecular halogen bonding supported by an aryldiyne linker.
The Journal of organic chemistry, 2014, 79, 6269-6278
4029633 CIFC24 H11 F4 I O2P 1 21/c 110.581; 25.437; 7.4819
90; 101.72; 90		1971.8Widner, Danielle L.; Knauf, Qianwei R.; Merucci, Mark T.; Fritz, Thomas R.; Sauer, Jon S.; Speetzen, Erin D.; Bosch, Eric; Bowling, Nathan P.
Intramolecular halogen bonding supported by an aryldiyne linker.
The Journal of organic chemistry, 2014, 79, 6269-6278
4029634 CIFC25 H14 Cl F3 O2P -17.4366; 10.2527; 13.9827
102.272; 101.077; 102.529		984.72Widner, Danielle L.; Knauf, Qianwei R.; Merucci, Mark T.; Fritz, Thomas R.; Sauer, Jon S.; Speetzen, Erin D.; Bosch, Eric; Bowling, Nathan P.
Intramolecular halogen bonding supported by an aryldiyne linker.
The Journal of organic chemistry, 2014, 79, 6269-6278
4029635 CIFC25 H10 Br F4 NP 1 21/c 111.1682; 7.7306; 21.808
90; 101.726; 90		1843.5Widner, Danielle L.; Knauf, Qianwei R.; Merucci, Mark T.; Fritz, Thomas R.; Sauer, Jon S.; Speetzen, Erin D.; Bosch, Eric; Bowling, Nathan P.
Intramolecular halogen bonding supported by an aryldiyne linker.
The Journal of organic chemistry, 2014, 79, 6269-6278
4029636 CIFC25 H10 F4 I NP -18.1996; 11.0966; 21.8061
76.617; 80.379; 88.778		1902.75Widner, Danielle L.; Knauf, Qianwei R.; Merucci, Mark T.; Fritz, Thomas R.; Sauer, Jon S.; Speetzen, Erin D.; Bosch, Eric; Bowling, Nathan P.
Intramolecular halogen bonding supported by an aryldiyne linker.
The Journal of organic chemistry, 2014, 79, 6269-6278
4029637 CIFC12 H9 N3P c a 218.357; 10.5669; 10.885
90; 90; 90		961.23Takagi, Koji; Al-Amin, Mohammad; Hoshiya, Naoyuki; Wouters, Johan; Sugimoto, Hiroshi; Shiro, Yoshitsugu; Fukuda, Hayato; Shuto, Satoshi; Arisawa, Mitsuhiro
Palladium-Nanoparticle-Catalyzed 1,7-Palladium Migration Involving C-H Activation, Followed by Intramolecular Amination: Regioselective Synthesis of N1-Arylbenzotriazoles and an Evaluation of Their Inhibitory Activity toward Indoleamine 2,3-Dioxygenase.
The Journal of organic chemistry, 2014, 79, 6366-6371
4029638 CIFC19 H14 O4P -18.048; 8.856; 11.42
83.591; 83.761; 69.162		753.9Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029639 CIFC24 H22 O4P 1 21/c 111.8725; 13.22; 12.4188
90; 102.876; 90		1900.2Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029640 CIFC24 H16 O4P -111.919; 12.417; 14.246
65.888; 68.574; 80.752		1791.3Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029641 CIFC24 H16 O4P 1 21/c 117.8867; 13.1372; 7.7251
90; 90.981; 90		1815Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029642 CIFC20 H16 O4C 1 2/c 117.3561; 7.9958; 12.4699
90; 115.147; 90		1566.5Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029643 CIFC21 H18 O4P 1 21/c 112.5816; 15.5161; 18.1947
90; 97.332; 90		3522.9Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029644 CIFC16 H14 O2P 1 21/c 112.3999; 4.6759; 22.7022
90; 105.674; 90		1267.34Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029645 CIFC25 H18 O4P -17.693; 11.2962; 11.8573
74.464; 71.929; 83.348		943.2Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029646 CIFC20 H14 O4C 1 2/c 131.285; 12.3872; 9.6298
90; 104.768; 90		3608.6Menning, Sebastian; Krämer, Maximilian; Duckworth, Andrew; Rominger, Frank; Beeby, Andrew; Dreuw, Andreas; Bunz, Uwe H. F.
Bridged tolanes: a twisted tale.
The Journal of organic chemistry, 2014, 79, 6571-6578
4029647 CIFC17 H19 Br O5P 1 21/c 19.6418; 27.8197; 13.1253
90; 109.997; 90		3308.37Alvarez-Fernández, Ana; Suárez-Rodríguez, Tatiana; Suárez-Sobrino, Angel L
Nucleophilic Addition/Double Cyclization Cascade Processes between Enynyl Fischer Carbene Complexes and Alkynyl Malonates.
The Journal of organic chemistry, 2014, 79, 6419-6423
4029648 CIFC20 H20 O5P 1 21/c 18.5989; 7.9316; 25.5665
90; 91.71; 90		1742.94Alvarez-Fernández, Ana; Suárez-Rodríguez, Tatiana; Suárez-Sobrino, Angel L
Nucleophilic Addition/Double Cyclization Cascade Processes between Enynyl Fischer Carbene Complexes and Alkynyl Malonates.
The Journal of organic chemistry, 2014, 79, 6419-6423
4029649 CIFC19 H24 O5P -17.69; 10.0039; 11.5864
69.737; 83.163; 80.305		822.46Alvarez-Fernández, Ana; Suárez-Rodríguez, Tatiana; Suárez-Sobrino, Angel L
Nucleophilic Addition/Double Cyclization Cascade Processes between Enynyl Fischer Carbene Complexes and Alkynyl Malonates.
The Journal of organic chemistry, 2014, 79, 6419-6423
4029650 CIFC12 H12 N2 OC 1 2/c 117.184; 10.142; 12.177
90; 106.912; 90		2030.4Zhang, Yan; Zheng, Jing; Cui, Sunliang
Rh(III)-Catalyzed C-H Activation/Cyclization of Indoles and Pyrroles: Divergent Synthesis of Heterocycles.
The Journal of organic chemistry, 2014, 79, 6490-6500
4029651 CIFC15 H16 N2 OP 1 21/c 19.0763; 12.2352; 12.0706
90; 107.042; 90		1281.59Zhang, Yan; Zheng, Jing; Cui, Sunliang
Rh(III)-Catalyzed C-H Activation/Cyclization of Indoles and Pyrroles: Divergent Synthesis of Heterocycles.
The Journal of organic chemistry, 2014, 79, 6490-6500
4029652 CIFC18 H14 N2 O3P -17.924; 10.1644; 11.0285
110.602; 110.187; 95.953		754.32Zhang, Yan; Zheng, Jing; Cui, Sunliang
Rh(III)-Catalyzed C-H Activation/Cyclization of Indoles and Pyrroles: Divergent Synthesis of Heterocycles.
The Journal of organic chemistry, 2014, 79, 6490-6500
4029653 CIFC43 H49 Cl3 N5 Na O6P -112.3245; 12.522; 16.8567
99.594; 110.951; 104.075		2262.27Lee, Jung Ha; Lee, Ji Hyun; Choi, Ye Rin; Kang, Philjae; Choi, Moon-Gun; Jeong, Kyu-Sung
Synthetic K+/Cl—Selective Symporter across a Phospholipid Membrane
The Journal of Organic Chemistry, 2014, 79, 6403
4029656 CIFC11 H16 O3P 1 21/c 16.282; 25.09; 6.268
90; 94.09; 90		985Liang, Demin; Zou, Yue; Wang, Quanrui; Goeke, Andreas
Sequential Diels-Alder Reaction/Rearrangement Sequence: Synthesis of Functionalized Bicyclo[2.2.1]heptane Derivatives and Revision of Their Relative Configuration.
The Journal of organic chemistry, 2014, 79, 6726-6731
4029657 CIFC17 H21 N O4P -16.082; 11.612; 12.591
66.576; 79.752; 88.139		802.2Liang, Demin; Zou, Yue; Wang, Quanrui; Goeke, Andreas
Sequential Diels-Alder Reaction/Rearrangement Sequence: Synthesis of Functionalized Bicyclo[2.2.1]heptane Derivatives and Revision of Their Relative Configuration.
The Journal of organic chemistry, 2014, 79, 6726-6731
4029658 CIFC19 H12 Br NP 1 21/c 17.9306; 15.123; 12.1926
90; 105.512; 90		1409Bentley, Keith W.; Wolf, Christian
Comprehensive Chirality Sensing: Development of Stereodynamic Probes with a Dual (Chir)optical Response.
The Journal of organic chemistry, 2014, 79, 6517-6531
4029659 CIFC18 H12 Br O2C 1 2/c 121.461; 7.9205; 16.9348
90; 103.402; 90		2800.2Bentley, Keith W.; Wolf, Christian
Comprehensive Chirality Sensing: Development of Stereodynamic Probes with a Dual (Chir)optical Response.
The Journal of organic chemistry, 2014, 79, 6517-6531
4029660 CIFC41 H31 Cl3 N2 O3P 21 21 2112.362; 14.611; 19.273
90; 90; 90		3481.1Bentley, Keith W.; Wolf, Christian
Comprehensive Chirality Sensing: Development of Stereodynamic Probes with a Dual (Chir)optical Response.
The Journal of organic chemistry, 2014, 79, 6517-6531
4029661 CIFC32 H22 O2P 21 21 219.3196; 14.6659; 15.9831
90; 90; 90		2184.6Bentley, Keith W.; Wolf, Christian
Comprehensive Chirality Sensing: Development of Stereodynamic Probes with a Dual (Chir)optical Response.
The Journal of organic chemistry, 2014, 79, 6517-6531
4029662 CIFC48 H34 N4P -19.841; 10.425; 19.35
78.097; 89.125; 73.819		1863.6Lu, Xuefeng; Fan, Suhua; Wu, Jinhong; Jia, Xiaowei; Wang, Zhong-Sheng; Zhou, Gang
Controlling the charge transfer in d-a-d chromophores based on pyrazine derivatives.
The Journal of organic chemistry, 2014, 79, 6480-6489
4029663 CIFC48 H34 N4P -110.685; 11.672; 15.495
71.759; 83.525; 79.61		1802Lu, Xuefeng; Fan, Suhua; Wu, Jinhong; Jia, Xiaowei; Wang, Zhong-Sheng; Zhou, Gang
Controlling the charge transfer in d-a-d chromophores based on pyrazine derivatives.
The Journal of organic chemistry, 2014, 79, 6480-6489
4029664 CIFC22 H21 N O3 SP 1 21/n 110.2238; 16.902; 10.8891
90; 94.605; 90		1875.6Ghorai, Manas K.; Sahoo, Ashis Kumar; Bhattacharyya, Aditya
Syntheses of Imidazo-, Oxa-, and Thiazepine Ring Systems via Ring-Opening of Aziridines/Cu-Catalyzed C-N/C-C Bond Formation.
The Journal of organic chemistry, 2014, 79, 6468-6479
4029665 CIFC29 H26 N2 O2 SP -110.604; 10.677; 11.678
66.35; 80.173; 74.336		1163.2Ghorai, Manas K.; Sahoo, Ashis Kumar; Bhattacharyya, Aditya
Syntheses of Imidazo-, Oxa-, and Thiazepine Ring Systems via Ring-Opening of Aziridines/Cu-Catalyzed C-N/C-C Bond Formation.
The Journal of organic chemistry, 2014, 79, 6468-6479
4029666 CIFC40 H27 N7 NiP -19.5758; 11.8423; 13.6132
99.878; 91.632; 100.298		1493.56Devillers, Charles H.; Hebié, Seydou; Lucas, Dominique; Cattey, Hélène; Clément, Sébastien; Richeter, Sébastien
Aromatic Nucleophilic Substitution (SNAr) of meso-Nitroporphyrin with Azide and Amines as an Alternative Metal Catalyst Free Synthetic Approach To Obtain meso-N-Substituted Porphyrins.
The Journal of organic chemistry, 2014, 79, 6424-6434

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