Crystallography Open Database

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4033925 CIFC35 H39 Cl N2 O5 PdP 1 21/c 114.8333; 33.6758; 7.13456
90; 98.9993; 90
3520.01Galenko, Ekaterina E.; Novikov, Mikhail S.; Shakirova, Firuza M.; Shakirova, Julia R.; Kornyakov, Ilya V.; Bodunov, Vladimir A.; Khlebnikov, Alexander F.
Isoxazole Strategy for the Synthesis of 2,2'-Bipyridine Ligands: Symmetrical and Unsymmetrical 6,6'-Binicotinates, 2,2'-Bipyridine-5-carboxylates, and Their Metal Complexes.
The Journal of organic chemistry, 2019, 84, 3524-3536
4033926 CIFC28 H20 Cl3 N3 O4 PdP 1 21/c 115.7195; 15.3316; 10.94788
90; 92.1608; 90
2636.62Galenko, Ekaterina E.; Novikov, Mikhail S.; Shakirova, Firuza M.; Shakirova, Julia R.; Kornyakov, Ilya V.; Bodunov, Vladimir A.; Khlebnikov, Alexander F.
Isoxazole Strategy for the Synthesis of 2,2'-Bipyridine Ligands: Symmetrical and Unsymmetrical 6,6'-Binicotinates, 2,2'-Bipyridine-5-carboxylates, and Their Metal Complexes.
The Journal of organic chemistry, 2019, 84, 3524-3536
4033927 CIFC22 H16 N2 O4 S2P 1 21/n 114.6496; 8.8096; 16.5349
90; 111.902; 90
1979.93Galenko, Ekaterina E.; Novikov, Mikhail S.; Shakirova, Firuza M.; Shakirova, Julia R.; Kornyakov, Ilya V.; Bodunov, Vladimir A.; Khlebnikov, Alexander F.
Isoxazole Strategy for the Synthesis of 2,2'-Bipyridine Ligands: Symmetrical and Unsymmetrical 6,6'-Binicotinates, 2,2'-Bipyridine-5-carboxylates, and Their Metal Complexes.
The Journal of organic chemistry, 2019, 84, 3524-3536
4033928 CIFC11 H13 Cl N2 O2P n m a17.2486; 10.17867; 6.17147
90; 90; 90
1083.51Ebule, Rene; Mudshinge, Sagar; Nantz, Michael H.; Mashuta, Mark S.; Hammond, Gerald B.; Xu, Bo
A 5 + 1 Protic Acid Assisted Aza-Pummerer Approach for Synthesis of 4-Chloropiperidines from Homoallylic Amines.
The Journal of organic chemistry, 2019, 84, 3249-3259
4033929 CIFC29 H25 N O2P 1 21/c 113.95; 11.207; 15.265
90; 112.269; 90
2208.5Chen, Shanping; Jiang, Pingyu; Wang, Pu; Pei, Yong; Huang, Huawen; Xiao, Fuhong; Deng, Guo-Jun
Three-Component Cascade Synthesis of Carbazoles through [1s,6s] Sigmatropic Shift under Metal-Free Conditions.
The Journal of organic chemistry, 2019, 84, 3121-3131
4033930 CIFC41 H47 I3 O2 S12P c a 2126.475; 10.6566; 18.45
90; 90; 90
5205.4Fleck, Nico; Hett, Tobias; Brode, Jonas; Meyer, Andreas; Richert, Sabine; Schiemann, Olav
C-C Cross-Coupling Reactions of Trityl Radicals: Spin Density Delocalization, Exchange Coupling, and a Spin Label.
The Journal of organic chemistry, 2019, 84, 3293-3303
4033931 CIFC14 H16 N2 O3P 1 21/c 110.4114; 7.6195; 16.5784
90; 103.281; 90
1279.99Yang, Zhen; Jiang, Kun; Chen, Ying-Chun; Wei, Ye
Copper-Catalyzed Dihydroquinolinone Synthesis from Isocyanides and O-Benzoyl Hydroxylamines.
The Journal of organic chemistry, 2019, 84, 3725-3734
4033932 CIFC11 H8 Br I O2P 1 21/c 110.7766; 7.8221; 13.4995
90; 94.552; 90
1134.36Gholap, Sachin P.; Jangid, Dashrath; Fernandes, Rodney A.
Metal-Free Brønsted Acid-Catalyzed Rearrangement of δ-Hydroxyalkynones to 2,3-Dihydro-4 H-pyran-4-ones: Total Synthesis of Obolactone and a Catechol Pyran Isolated from Plectranthus sylvestris.
The Journal of organic chemistry, 2019, 84, 3537-3551
4033933 CIFC11 H8 Br2 O2P 1 21/c 110.6794; 7.5795; 13.4516
90; 92.023; 90
1088.15Gholap, Sachin P.; Jangid, Dashrath; Fernandes, Rodney A.
Metal-Free Brønsted Acid-Catalyzed Rearrangement of δ-Hydroxyalkynones to 2,3-Dihydro-4 H-pyran-4-ones: Total Synthesis of Obolactone and a Catechol Pyran Isolated from Plectranthus sylvestris.
The Journal of organic chemistry, 2019, 84, 3537-3551
4033934 CIFC11 H8 Br Cl O2P 1 21/c 110.7391; 7.356; 13.5262
90; 90.473; 90
1068.49Gholap, Sachin P.; Jangid, Dashrath; Fernandes, Rodney A.
Metal-Free Brønsted Acid-Catalyzed Rearrangement of δ-Hydroxyalkynones to 2,3-Dihydro-4 H-pyran-4-ones: Total Synthesis of Obolactone and a Catechol Pyran Isolated from Plectranthus sylvestris.
The Journal of organic chemistry, 2019, 84, 3537-3551
4033935 CIFC15 H22 O2P 1 21/c 121.409; 5.8925; 10.5126
90; 98.052; 90
1313.1Gholap, Sachin P.; Jangid, Dashrath; Fernandes, Rodney A.
Metal-Free Brønsted Acid-Catalyzed Rearrangement of δ-Hydroxyalkynones to 2,3-Dihydro-4 H-pyran-4-ones: Total Synthesis of Obolactone and a Catechol Pyran Isolated from Plectranthus sylvestris.
The Journal of organic chemistry, 2019, 84, 3537-3551
4033936 CIFC9 H7 Cl O3P n a 216.7921; 24.5033; 10.1829
90; 90; 90
1694.73Gholap, Sachin P.; Jangid, Dashrath; Fernandes, Rodney A.
Metal-Free Brønsted Acid-Catalyzed Rearrangement of δ-Hydroxyalkynones to 2,3-Dihydro-4 H-pyran-4-ones: Total Synthesis of Obolactone and a Catechol Pyran Isolated from Plectranthus sylvestris.
The Journal of organic chemistry, 2019, 84, 3537-3551
4033937 CIFC12 H10 O4P 1 21/c 15.4376; 9.2746; 19.1403
90; 97.111; 90
957.85Gholap, Sachin P.; Jangid, Dashrath; Fernandes, Rodney A.
Metal-Free Brønsted Acid-Catalyzed Rearrangement of δ-Hydroxyalkynones to 2,3-Dihydro-4 H-pyran-4-ones: Total Synthesis of Obolactone and a Catechol Pyran Isolated from Plectranthus sylvestris.
The Journal of organic chemistry, 2019, 84, 3537-3551
4033938 CIFC25 H21 N3P 1 21/c 15.5637; 16.8977; 19.6894
90; 97.368; 90
1835.8Chang, Meng-Yang; Wu, Yan-Shin
HOAc-Mediated Cyclocondensation of 2-Formylazaarenes and Cyclic Amines. Synthesis of Pyrrolo[1,2- a]azaarenes.
The Journal of organic chemistry, 2019, 84, 3638-3646
4033939 CIFC35 H27 N5P -19.4459; 11.1306; 13.0768
98.277; 90.181; 106.478
1303.27Chang, Meng-Yang; Wu, Yan-Shin
HOAc-Mediated Cyclocondensation of 2-Formylazaarenes and Cyclic Amines. Synthesis of Pyrrolo[1,2- a]azaarenes.
The Journal of organic chemistry, 2019, 84, 3638-3646
4033940 CIFC39 H35 N5P 1 21/c 19.9444; 30.8977; 10.1941
90; 103.583; 90
3044.6Chang, Meng-Yang; Wu, Yan-Shin
HOAc-Mediated Cyclocondensation of 2-Formylazaarenes and Cyclic Amines. Synthesis of Pyrrolo[1,2- a]azaarenes.
The Journal of organic chemistry, 2019, 84, 3638-3646
4033941 CIFC15 H10 N2P 1 21/c 111.5095; 6.0108; 15.9991
90; 109.073; 90
1046.08Chang, Meng-Yang; Wu, Yan-Shin
HOAc-Mediated Cyclocondensation of 2-Formylazaarenes and Cyclic Amines. Synthesis of Pyrrolo[1,2- a]azaarenes.
The Journal of organic chemistry, 2019, 84, 3638-3646
4033942 CIFC20 H13 Br N2 O6P 21 21 218.1343; 11.9258; 18.2918
90; 90; 90
1774.45Suresh, Alati; Baiju, Thekke V.; Kumar, Tarun; Namboothiri, Irishi N. N.
Synthesis of Spiro- and Fused Heterocycles via (4+4) Annulation of Sulfonylphthalide with o-Hydroxystyrenyl Derivatives.
The Journal of organic chemistry, 2019, 84, 3158-3168
4033943 CIFC20 H13 Br N2 O6P -16.90037; 7.8322; 16.9797
82.7874; 85.8772; 79.2104
893.21Suresh, Alati; Baiju, Thekke V.; Kumar, Tarun; Namboothiri, Irishi N. N.
Synthesis of Spiro- and Fused Heterocycles via (4+4) Annulation of Sulfonylphthalide with o-Hydroxystyrenyl Derivatives.
The Journal of organic chemistry, 2019, 84, 3158-3168
4033944 CIFC30 H19 Br O6 SP -17.8843; 10.4889; 16.211
80.468; 87.624; 73.089
1264.9Suresh, Alati; Baiju, Thekke V.; Kumar, Tarun; Namboothiri, Irishi N. N.
Synthesis of Spiro- and Fused Heterocycles via (4+4) Annulation of Sulfonylphthalide with o-Hydroxystyrenyl Derivatives.
The Journal of organic chemistry, 2019, 84, 3158-3168
4033945 CIFC156 H162P 1 21/m 118.83; 32.96; 18.84
90; 119.64; 90
10163Sun, Zhe; Mio, Tatsuru; Ikemoto, Koki; Sato, Sota; Isobe, Hiroyuki
Synthesis, Structures, and Assembly of Geodesic Phenine Frameworks with Isoreticular Networks of [ n]Cyclo- para-phenylenes.
The Journal of organic chemistry, 2019, 84, 3500-3507
4033946 CIFC260 H270P 1 21 116.57; 42.93; 57.47
90; 96.72; 90
40600Sun, Zhe; Mio, Tatsuru; Ikemoto, Koki; Sato, Sota; Isobe, Hiroyuki
Synthesis, Structures, and Assembly of Geodesic Phenine Frameworks with Isoreticular Networks of [ n]Cyclo- para-phenylenes.
The Journal of organic chemistry, 2019, 84, 3500-3507
4033947 CIFC208 H216C c c a :230.56; 35.21; 22.18
90; 90; 90
23866Sun, Zhe; Mio, Tatsuru; Ikemoto, Koki; Sato, Sota; Isobe, Hiroyuki
Synthesis, Structures, and Assembly of Geodesic Phenine Frameworks with Isoreticular Networks of [ n]Cyclo- para-phenylenes.
The Journal of organic chemistry, 2019, 84, 3500-3507
4033948 CIFC180 H210 Cl24P 1 21/m 118.83; 32.96; 18.84
90; 119.64; 90
10163Sun, Zhe; Mio, Tatsuru; Ikemoto, Koki; Sato, Sota; Isobe, Hiroyuki
Synthesis, Structures, and Assembly of Geodesic Phenine Frameworks with Isoreticular Networks of [ n]Cyclo- para-phenylenes.
The Journal of organic chemistry, 2019, 84, 3500-3507
4033949 CIFC218 H226 Cl30C c c a :230.56; 35.21; 22.18
90; 90; 90
23866Sun, Zhe; Mio, Tatsuru; Ikemoto, Koki; Sato, Sota; Isobe, Hiroyuki
Synthesis, Structures, and Assembly of Geodesic Phenine Frameworks with Isoreticular Networks of [ n]Cyclo- para-phenylenes.
The Journal of organic chemistry, 2019, 84, 3500-3507
4033950 CIFC460 H251 Cl7P -119.82; 20.51; 38.69
81.65; 78.06; 77.99
14965Sun, Zhe; Mio, Tatsuru; Ikemoto, Koki; Sato, Sota; Isobe, Hiroyuki
Synthesis, Structures, and Assembly of Geodesic Phenine Frameworks with Isoreticular Networks of [ n]Cyclo- para-phenylenes.
The Journal of organic chemistry, 2019, 84, 3500-3507
4033951 CIFC28 H22 Cl N O5C 1 2/c 128.1237; 10.7016; 16.0023
90; 94.248; 90
4803Fernández, Patricia; Valdés, Carlos; Fañanás, Francisco J; Rodríguez, Félix
Unusual Reactivity of Isoquinolinones Generated by Silver-Catalyzed Cycloisomerizations of Imines Derived from ortho-Alkynylsalicylaldehydes.
The Journal of organic chemistry, 2019, 84, 3184-3191
4033952 CIFC31 H30 Br N O9P -110.3778; 11.0907; 14.7661
75.263; 76.775; 67.089
1497.82Fernández, Patricia; Valdés, Carlos; Fañanás, Francisco J; Rodríguez, Félix
Unusual Reactivity of Isoquinolinones Generated by Silver-Catalyzed Cycloisomerizations of Imines Derived from ortho-Alkynylsalicylaldehydes.
The Journal of organic chemistry, 2019, 84, 3184-3191
4033953 CIFC18 H14 N2 O2P 21 21 219.0692; 9.9319; 15.9479
90; 90; 90
1436.5Sengoku, Tetsuya; Shirai, Anna; Takano, Ayaka; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi
Divergent Synthesis of Methylene Lactone- and Methylene Lactam-Based Spiro Compounds: Utility of Amido-Functionalized γ-Hydroxylactam as a Precursor for Cytotoxic <i>N</i>,<i>O</i>- and <i>N</i>,<i>N</i>-Spiro Compounds.
The Journal of organic chemistry, 2019, 84, 12532-12541
4033954 CIFC19 H22 B N O3P 1 21/c 111.756; 17.147; 9.519
90; 113.778; 90
1756Sengoku, Tetsuya; Shirai, Anna; Takano, Ayaka; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi
Divergent Synthesis of Methylene Lactone- and Methylene Lactam-Based Spiro Compounds: Utility of Amido-Functionalized γ-Hydroxylactam as a Precursor for Cytotoxic <i>N</i>,<i>O</i>- and <i>N</i>,<i>N</i>-Spiro Compounds.
The Journal of organic chemistry, 2019, 84, 12532-12541
4033955 CIFC15 H20 B N O3P b c a10.5088; 10.1424; 27.846
90; 90; 90
2968Sengoku, Tetsuya; Shirai, Anna; Takano, Ayaka; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi
Divergent Synthesis of Methylene Lactone- and Methylene Lactam-Based Spiro Compounds: Utility of Amido-Functionalized γ-Hydroxylactam as a Precursor for Cytotoxic <i>N</i>,<i>O</i>- and <i>N</i>,<i>N</i>-Spiro Compounds.
The Journal of organic chemistry, 2019, 84, 12532-12541
4033956 CIFC16 H22 B N O3P 1 21/c 114.8806; 10.6387; 10.1915
90; 97.091; 90
1601.1Sengoku, Tetsuya; Shirai, Anna; Takano, Ayaka; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi
Divergent Synthesis of Methylene Lactone- and Methylene Lactam-Based Spiro Compounds: Utility of Amido-Functionalized γ-Hydroxylactam as a Precursor for Cytotoxic <i>N</i>,<i>O</i>- and <i>N</i>,<i>N</i>-Spiro Compounds.
The Journal of organic chemistry, 2019, 84, 12532-12541
4033957 CIFC19 H28 B N O3P 1 21/c 111.9881; 16.7094; 9.6243
90; 90.162; 90
1927.87Sengoku, Tetsuya; Shirai, Anna; Takano, Ayaka; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi
Divergent Synthesis of Methylene Lactone- and Methylene Lactam-Based Spiro Compounds: Utility of Amido-Functionalized γ-Hydroxylactam as a Precursor for Cytotoxic <i>N</i>,<i>O</i>- and <i>N</i>,<i>N</i>-Spiro Compounds.
The Journal of organic chemistry, 2019, 84, 12532-12541
4033958 CIFC17 H9 F3 N2P -17.431; 8.205; 12.763
79.853; 80.198; 71.077
719.2Chen, Zhengwang; Liang, Pei; Xu, Fan; Deng, Zhen; Long, Lipeng; Luo, Guotian; Ye, Min
Metal-Free Aminothiation of Alkynes: Three-Component Tandem Annulation toward Indolizine Thiones from 2-Alkylpyridines, Ynals, and Elemental Sulfur.
The Journal of organic chemistry, 2019, 84, 12639-12647
4033959 CIFC22 H16 N2 OP 1 21/c 18.8092; 11.4234; 17.0959
90; 101.841; 90
1683.77Aksenov, Alexander V.; Aksenov, Dmitrii A.; Aksenov, Nicolai A.; Aleksandrova, Elena V.; Rubin, Michael
Preparation of Stereodefined 2-(3-Oxoindolin-2-yl)-2-Arylacetonitriles via One-Pot Reaction of Indoles with Nitroalkenes.
The Journal of organic chemistry, 2019, 84, 12420-12429
4033960 CIFC23 H18 N2 OP 1 21/n 19.3188; 7.4995; 25.0534
90; 99.986; 90
1724.36Aksenov, Alexander V.; Aksenov, Dmitrii A.; Aksenov, Nicolai A.; Aleksandrova, Elena V.; Rubin, Michael
Preparation of Stereodefined 2-(3-Oxoindolin-2-yl)-2-Arylacetonitriles via One-Pot Reaction of Indoles with Nitroalkenes.
The Journal of organic chemistry, 2019, 84, 12420-12429
4033961 CIFC29 H25 N3 O6P 1 21 113.0203; 6.0434; 16.2047
90; 101.8; 90
1248.2Ramaraju, Panduga; Pawar, Amol Prakash; Iype, Eldhose; Mir, Nisar A.; Choudhary, Sachin; Sharma, Devinder Kumar; Kant, Rajni; Kumar, Indresh
Enantio- and Diastereoselective Two-Pot Synthesis of Isoquinuclidines from Glutaraldehyde and <i>N</i>-Aryl Imines with DFT Calculations.
The Journal of organic chemistry, 2019, 84, 12408-12419
4033962 CIFC56 H71 O3 PP 1 21/n 112.5922; 28.656; 13.3383
90; 100.726; 90
4728.9Wagen, Corin C.; Ingoglia, Bryan T.; Buchwald, Stephen L.
Unexpected Formation of Hexasubstituted Arenes through a 2-fold Palladium-Mediated Ligand Arylation.
The Journal of organic chemistry, 2019, 84, 12672-12679
4033963 CIFC25 H25 N O3 S SeP 1 21/n 110.8819; 11.2677; 19.934
90; 92.701; 90
2441.5Zhang, Rong; Xu, Pei; Wang, Shun-Yi; Ji, Shun-Jun
Visible Light-Induced Co- or Cu-Catalyzed Selenosulfonylation of Alkynes: Synthesis of β-(Seleno)vinyl Sulfones.
The Journal of organic chemistry, 2019, 84, 12324-12333
4033964 CIFC23 H20 O4 S SeP 1 21/c 18.486; 15.1787; 16.604
90; 97.43; 90
2120.7Zhang, Rong; Xu, Pei; Wang, Shun-Yi; Ji, Shun-Jun
Visible Light-Induced Co- or Cu-Catalyzed Selenosulfonylation of Alkynes: Synthesis of β-(Seleno)vinyl Sulfones.
The Journal of organic chemistry, 2019, 84, 12324-12333
4033965 CIFC20 H17 F N2P 21 21 2110.1757; 10.8768; 13.9556
90; 90; 90
1544.59Guan, Xu-Kai; Zhang, Heng; Gao, Ji-Gang; Sun, Dong-Yang; Qin, Xiang-Shuo; Jiang, Guo-Feng; Zhang, Guang-Liang; Zhang, Suoqin
Asymmetric Synthesis of 1,1,1-Triarylethanes by Chiral Imidodiphosphoric Acid Catalyzed Nucleophilic Addition of Pyrrole and Indoles to 3-Vinylindoles.
The Journal of organic chemistry, 2019, 84, 12562-12572
4033966 CIFC16 H15 I O2P 1 21/c 16.6474; 25.6822; 8.2626
90; 90.123; 90
1410.59Li, Mengxue; Yang, Fang; Yuan, Ting; Li, Haoyang; Li, Jian; Chen, Zi-Sheng; Ji, Kegong
Syntheses of <i>Z</i>-Iodovinylfurans and 2-Acyl Furans via Controllable Cyclization of Ynenones.
The Journal of organic chemistry, 2019, 84, 12617-12625
4033967 CIFC27 H24 N2 O SP 1 21/c 17.3362; 12.5626; 24.8378
90; 96.443; 90
2274.64Shen, Shou-Jie; Du, Xiao-Li; Xu, Xiao-Li; Zhao, Ming-Gang; Liang, Jin-Yan
Regioselective N-Addition/Substitution Reaction of α-Alkylidene Pyrazolinones with Propargyl Sulfonium Salts to Construct Allylthio-Containing Pyrazolones.
The Journal of organic chemistry, 2019, 84, 12520-12531
4033968 CIFC26 H21 Br N2 OP 1 21/c 17.0382; 12.4284; 25.3081
90; 95.463; 90
2203.73Shen, Shou-Jie; Du, Xiao-Li; Xu, Xiao-Li; Zhao, Ming-Gang; Liang, Jin-Yan
Regioselective N-Addition/Substitution Reaction of α-Alkylidene Pyrazolinones with Propargyl Sulfonium Salts to Construct Allylthio-Containing Pyrazolones.
The Journal of organic chemistry, 2019, 84, 12520-12531
4033969 CIFC16 H13 N O3P 4/n :214.3246; 14.3246; 13.4826
90; 90; 90
2766.55Chen, Donghan; Yao, Yongqi; Yang, Wen; Lin, Qifu; Li, Huanyong; Wang, Lin; Chen, Shuqi; Tan, Yun; Yang, Dingqiao
Palladium-Catalyzed <i>syn</i>-Stereocontrolled Ring Opening of Oxabicyclic Alkenes with Arylsulfonyl Hydrazides.
The Journal of organic chemistry, 2019, 84, 12481-12489
4033970 CIFC37 H15 F16 O2 PP 1 21 112.8387; 8.758; 15.1578
90; 107.408; 90
1626.3Fujii, Kohei; Ito, Shigekazu; Mikami, Koichi
Synthetic Methodologies for Perfluoroaryl-Substituted (Diaryl)methylphosphonates, -Phosphinates via S<sub>N</sub>Ar Reaction.
The Journal of organic chemistry, 2019, 84, 12281-12291
4033971 CIFC27 H47 N O5 S SiP -111.3319; 12.7598; 12.8305
110.192; 106.603; 101.611
1573.1Domin, Sylwia; Plata, Paulina; ZambroĊ„, Bartosz K
Diastereoselectivity Switch in the Pd(0)/InI-Mediated Reactions of β-Lactams with Aldehydes: An Entry into Nonracemic Semiprotected (3<i>E</i>)-2,6-Enediols.
The Journal of organic chemistry, 2019, 84, 12268-12280
4033972 CIFC11 H8 O4P 1 21/c 111.629; 6.594; 11.819
90; 92.98; 90
905.1Pilevar, Afsaneh; Hosseini, Abolfazl; Becker, Jonathan; Schreiner, Peter R.
Syn-Dihydroxylation of Alkenes Using a Sterically Demanding Cyclic Diacyl Peroxide.
The Journal of organic chemistry, 2019, 84, 12377-12386
4033973 CIFC22 H26 O4P -17.8299; 10.6683; 12.3114
94.019; 106.392; 111.383
901.29Pilevar, Afsaneh; Hosseini, Abolfazl; Becker, Jonathan; Schreiner, Peter R.
Syn-Dihydroxylation of Alkenes Using a Sterically Demanding Cyclic Diacyl Peroxide.
The Journal of organic chemistry, 2019, 84, 12377-12386
4033974 CIFC37 H33 N O5P -110.3606; 12.1928; 12.3443
73.449; 82.756; 85.252
1481Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033975 CIFC43 H45 N O2P -18.8231; 12.02; 18.5392
100.516; 94.566; 101.37
1881.51Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033976 CIFC36 H34 N2 OP -112.465; 13.193; 18.105
85.557; 88.764; 82.243
2941.1Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033977 CIFC36 H34 N2 OC 1 2/c 133.92; 17.611; 12.341
90; 108.56; 90
6989Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033978 CIFC34 H28 Br2 N2 OP -112.8692; 14.8165; 18.1907
94.0352; 91.0074; 112.648
3189.4Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033979 CIFC35 H31 Cl N2 O3P -19.7033; 11.3031; 14.5288
109.456; 99.8627; 95.9068
1458.17Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033980 CIFC36 H33 Cl N2 O2P -110.215; 12.438; 13.289
66.026; 87.403; 73.883
1477.7Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033981 CIFC43 H38 N2 O2P -19.5778; 11.7023; 16.5026
73.919; 73.572; 84.413
1704.4Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033982 CIFC45 H42 N2 O2P -111.076; 12.665; 14.752
68.944; 75.455; 68.425
1778.9Huang, Ying; Fang, Hui-Lin; Huang, Yi-Xin; Sun, Jing; Yan, Chao-Guo
Synthesis of 7'-Arylidenespiro[indoline-3,1'-pyrrolizines] and 7'-Arylidenespiro[indene-2,1'-pyrrolizines] via [3 + 2] Cycloaddition and β-C-H Functionalized Pyrrolidine.
The Journal of organic chemistry, 2019, 84, 12437-12451
4033983 CIFC25 H26 Cl N3 O RuP c a 219.1; 14.3544; 17.5769
90; 90; 90
2295.98Sagara, Prateep Singh; Siril, Prem Felix; Ravikumar, Ponneri Chandrababu
<i>N</i>-Amino-7-azaindole as the <i>N</i>,<i>N</i>'-Bidentate Directing Group: Ruthenium-Catalyzed Oxidative Annulation of <i>N</i>-(7-Azaindole)benzamides with Alkynes via C-H Bond Activation.
The Journal of organic chemistry, 2019, 84, 12314-12323
4033984 CIFC24 H19 N3 OP -19.2805; 12.3962; 16.8806
107.261; 92.112; 95.307
1842.36Sagara, Prateep Singh; Siril, Prem Felix; Ravikumar, Ponneri Chandrababu
<i>N</i>-Amino-7-azaindole as the <i>N</i>,<i>N</i>'-Bidentate Directing Group: Ruthenium-Catalyzed Oxidative Annulation of <i>N</i>-(7-Azaindole)benzamides with Alkynes via C-H Bond Activation.
The Journal of organic chemistry, 2019, 84, 12314-12323
4033985 CIFC14 H11 N3 OP 1 21/c 111.8814; 19.457; 11.4871
90; 115.705; 90
2392.75Sagara, Prateep Singh; Siril, Prem Felix; Ravikumar, Ponneri Chandrababu
<i>N</i>-Amino-7-azaindole as the <i>N</i>,<i>N</i>'-Bidentate Directing Group: Ruthenium-Catalyzed Oxidative Annulation of <i>N</i>-(7-Azaindole)benzamides with Alkynes via C-H Bond Activation.
The Journal of organic chemistry, 2019, 84, 12314-12323
4033986 CIFC21 H24 Br N O6P -18.6904; 10.4377; 11.8142
79.06; 83.239; 75.759
1016.99Inuki, Shinsuke; Sato, Keisuke; Zui, Naoto; Yamaguchi, Ryosuke; Matsumaru, Takanori; Fujimoto, Yukari
Synthetic Studies on FNC-RED and Its Analogues Containing an All <i>syn</i>-Cyclopentanetetrol Moiety.
The Journal of organic chemistry, 2019, 84, 12680-12685
4033987 CIFC75 H14 O3P b c a16.7603; 16.2554; 27.9643
90; 90; 90
7618.7Wu, Yin-Fu; Wang, Shan-Shan; Yao, Chun-Rui; Chen, Zuo-Chang; Li, Shu-Hui; Yao, Yang-Rong; Zhang, Xue-Peng; Su, Yin; Deng, Shun-Liu; Zhang, Qianyan; Gao, Fei; Xie, Su-Yuan; Huang, Rong-Bin; Zheng, Lan-Sun
General One-step Synthesis of Symmetrical or Unsymmetrical 1,4-Di(organo)fullerenes from Organo(hydro)fullerenes through Direct Oxidative Arylation.
The Journal of organic chemistry, 2019, 84, 12259-12267
4033988 CIFC71 H12 O3 S2P 1 21/c 110.1156; 13.4679; 28.2219
90; 89.999; 90
3844.84Wu, Yin-Fu; Wang, Shan-Shan; Yao, Chun-Rui; Chen, Zuo-Chang; Li, Shu-Hui; Yao, Yang-Rong; Zhang, Xue-Peng; Su, Yin; Deng, Shun-Liu; Zhang, Qianyan; Gao, Fei; Xie, Su-Yuan; Huang, Rong-Bin; Zheng, Lan-Sun
General One-step Synthesis of Symmetrical or Unsymmetrical 1,4-Di(organo)fullerenes from Organo(hydro)fullerenes through Direct Oxidative Arylation.
The Journal of organic chemistry, 2019, 84, 12259-12267
4033989 CIFC38 H30 N2 O6P 1 21/c 118.719; 24.73; 13.634
90; 90.08; 90
6311Liu, Rongfang; Qin, Zifeng; Fan, Binbin; Li, Ruifeng; Zhou, Rong; He, Zhengjie
Phosphine-Catalyzed Chemo- and Diastereoselective [2 + 2 + 2] and [3 + 2] Annulations of γ-Methyl Allenoates with Doubly Activated Olefins: Syntheses of Highly Substituted Cyclohexanes and Cyclopentenes.
The Journal of organic chemistry, 2019, 84, 12490-12498
4033990 CIFC29 H28 N2 O6P 1 21/c 115.402; 12.284; 14.044
90; 101.07; 90
2607.7Liu, Rongfang; Qin, Zifeng; Fan, Binbin; Li, Ruifeng; Zhou, Rong; He, Zhengjie
Phosphine-Catalyzed Chemo- and Diastereoselective [2 + 2 + 2] and [3 + 2] Annulations of γ-Methyl Allenoates with Doubly Activated Olefins: Syntheses of Highly Substituted Cyclohexanes and Cyclopentenes.
The Journal of organic chemistry, 2019, 84, 12490-12498
4033991 CIFC23 H17 N3P 1 21/c 18.8801; 10.4479; 19.147
90; 91.163; 90
1776.06Li, Yong; Huang, Jiu-Hong; Wang, Juan-Li; Song, Gui-Ting; Tang, Dian-Yong; Yao, Fang; Lin, Hui-Kuan; Yan, Wei; Li, Hong-Yu; Xu, Zhi-Gang; Chen, Zhong-Zhu
Diversity-Oriented Synthesis of Imidazo-Dipyridines with Anticancer Activity via the Groebke-Blackburn-Bienaymé and TBAB-Mediated Cascade Reaction in One Pot.
The Journal of organic chemistry, 2019, 84, 12632-12638
4033992 CIFC21 H34 O4 SiP -111.8826; 14.0278; 14.7882
67.8036; 70.5153; 77.3415
2139.34Niu, Guang-Hao; Liu, Pin-Heng; Hung, Wei-Chun; Tseng, Ping-Yao; Chuang, Gary Jing
Formal Synthesis of (±)-Pentalenolactone A Methyl Ester.
The Journal of organic chemistry, 2019, 84, 10172-10182
4033993 CIFC14 H18 O3P 1 21/n 16.4887; 7.174; 25.6544
90; 93.117; 90
1192.44Niu, Guang-Hao; Liu, Pin-Heng; Hung, Wei-Chun; Tseng, Ping-Yao; Chuang, Gary Jing
Formal Synthesis of (±)-Pentalenolactone A Methyl Ester.
The Journal of organic chemistry, 2019, 84, 10172-10182
4033994 CIFC14 H17 O2P 1 21/n 17.6989; 14.1778; 12.0083
90; 105.433; 90
1263.48Niu, Guang-Hao; Liu, Pin-Heng; Hung, Wei-Chun; Tseng, Ping-Yao; Chuang, Gary Jing
Formal Synthesis of (±)-Pentalenolactone A Methyl Ester.
The Journal of organic chemistry, 2019, 84, 10172-10182
4033995 CIFC14 H18 O3P -16.5759; 7.0819; 13.0369
90.667; 99.802; 100.196
588.269Niu, Guang-Hao; Liu, Pin-Heng; Hung, Wei-Chun; Tseng, Ping-Yao; Chuang, Gary Jing
Formal Synthesis of (±)-Pentalenolactone A Methyl Ester.
The Journal of organic chemistry, 2019, 84, 10172-10182
4033996 CIFC14 H21 N O7 SP 21 21 217.7353; 12.3699; 17.0299
90; 90; 90
1629.5Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4033997 CIFC13 H19 N O7 SP 21 21 2117.1318; 11.3992; 7.7486
90; 90; 90
1513.21Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4033998 CIFC19 H23 N O5P 21 21 216.0414; 18.1188; 32.9664
90; 90; 90
3608.6Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4033999 CIFC20 H25 N O5P 21 21 217.9339; 9.5184; 50.1703
90; 90; 90
3788.76Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034000 CIFC20 H25 N O5P 21 21 217.4709; 9.7; 26.3803
90; 90; 90
1911.72Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034001 CIFC18 H23 N O4P 21 21 218.5022; 9.5737; 21.0075
90; 90; 90
1709.96Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034002 CIFC19 H25 N O4P 1 21 19.0485; 20.726; 9.711
90; 90.9436; 90
1820.95Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034003 CIFC13 H19 N O8 S2P 21 21 217.8667; 8.4699; 25.7707
90; 90; 90
1717.11Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034004 CIFC18 H22 Cl N O5 SP 1 21 111.8798; 7.2157; 12.259
90; 114.56; 90
955.8Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034005 CIFC13 H19 N O7 S2P 1 21 19.3561; 8.2582; 10.6327
90; 92.674; 90
820.64Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034006 CIFC19 H23 N O5 SP 21 21 216.8792; 9.6131; 27.6203
90; 90; 90
1826.54Bagum, Halima; Christensen, Kirsten E.; Genov, Miroslav; Pretsch, Alexander; Pretsch, Dagmar; Moloney, Mark G.
Synthetic Access to 3-Substituted Pyroglutamic Acids from Tetramate Derivatives of Serine, Threonine, <i>allo</i>-Threonine, and Cysteine.
The Journal of organic chemistry, 2019, 84, 10257-10279
4034007 CIFC16 H17 N O3 SP 1 21/c 115.819; 6.6125; 13.7597
90; 103.292; 90
1400.75Lee, Robert; Bashrum, Bryan; Cagle, Ethan C.; Walters, Jillian; Massey, Jake; Zanghi, Monica; Birchfield, Carolyn; French, David; Joy, Jessica; Dos Passos Gomes, Gabriel; Wiget, Paul A.
Electronic Donation or Steric Contraction: A Spectroscopic and Structural Analysis of Medium-Sized Constrained Rings for Potential Long-Range Hyperconjugation.
The Journal of organic chemistry, 2019, 84, 9897-9906
4034008 CIFC10 H12 O2P 1 21/c 19.0498; 6.4259; 14.3599
90; 100.944; 90
819.89Lee, Robert; Bashrum, Bryan; Cagle, Ethan C.; Walters, Jillian; Massey, Jake; Zanghi, Monica; Birchfield, Carolyn; French, David; Joy, Jessica; Dos Passos Gomes, Gabriel; Wiget, Paul A.
Electronic Donation or Steric Contraction: A Spectroscopic and Structural Analysis of Medium-Sized Constrained Rings for Potential Long-Range Hyperconjugation.
The Journal of organic chemistry, 2019, 84, 9897-9906
4034009 CIFC9 H10 O2P 1 21/c 16.2951; 10.3461; 10.9731
90; 95.099; 90
711.847Lee, Robert; Bashrum, Bryan; Cagle, Ethan C.; Walters, Jillian; Massey, Jake; Zanghi, Monica; Birchfield, Carolyn; French, David; Joy, Jessica; Dos Passos Gomes, Gabriel; Wiget, Paul A.
Electronic Donation or Steric Contraction: A Spectroscopic and Structural Analysis of Medium-Sized Constrained Rings for Potential Long-Range Hyperconjugation.
The Journal of organic chemistry, 2019, 84, 9897-9906
4034010 CIFC11 H14 OP c c n20.0831; 7.6632; 10.9517
90; 90; 90
1685.48Lee, Robert; Bashrum, Bryan; Cagle, Ethan C.; Walters, Jillian; Massey, Jake; Zanghi, Monica; Birchfield, Carolyn; French, David; Joy, Jessica; Dos Passos Gomes, Gabriel; Wiget, Paul A.
Electronic Donation or Steric Contraction: A Spectroscopic and Structural Analysis of Medium-Sized Constrained Rings for Potential Long-Range Hyperconjugation.
The Journal of organic chemistry, 2019, 84, 9897-9906
4034011 CIFC33 H30 Br N5 O4P 21 21 2113.207; 13.296; 34.839
90; 90; 90
6118Lin, Ye; Zhao, Bo-Liang; Du, Da-Ming
Bifunctional Squaramide-Catalyzed Asymmetric [3 + 2] Cyclization of 2-(1-Methyl-2-oxoindolin-3-yl)malononitriles with Unsaturated Pyrazolones To Construct Spirooxindole-Fused Spiropyrazolones.
The Journal of organic chemistry, 2019, 84, 10209-10220
4034012 CIFC12 H14 F3 N O2P 1 21 115.4743; 5.3473; 15.7831
90; 91.454; 90
1305.56Chen, Mu-Wang; Yang, Qin; Deng, Zhihong; Ding, Qiuping; Peng, Yiyuan
Synthesis of Chiral β-Fluoroalkyl β-Amino Acid Derivatives via Palladium-Catalyzed Hydrogenation.
The Journal of organic chemistry, 2019, 84, 10371-10379
4034013 CIFC7 H10 N2 O2 SP n a 2117.027; 7.4312; 6.8749
90; 90; 90
869.89Mamidala, Ramesh; Biswal, Priyabrata; Subramani, M. Siva; Samser, Shaikh; Venkatasubbaiah, Krishnan
Palladacycle-Phosphine Catalyzed Methylation of Amines and Ketones Using Methanol.
The Journal of organic chemistry, 2019, 84, 10472-10480
4034014 CIFC53 H37 Cl6 F12 N4 O4 Pd2P -112.6732; 15.4639; 16.0509
114.873; 96.893; 94.6
2803.2Mamidala, Ramesh; Biswal, Priyabrata; Subramani, M. Siva; Samser, Shaikh; Venkatasubbaiah, Krishnan
Palladacycle-Phosphine Catalyzed Methylation of Amines and Ketones Using Methanol.
The Journal of organic chemistry, 2019, 84, 10472-10480
4034015 CIFC24 H18 N2 O4P 1 21/c 129.2218; 9.7598; 20.4945
90; 91.601; 90
5842.7Kumar, Sandeep; Pradhan, Sourav; Roy, Subhasish; De, Pinaki Bhusan; Punniyamurthy, Tharmalingam
Iron-Catalyzed Regioselective Remote C(sp<sup>2</sup>)-H Carboxylation of Naphthyl and Quinoline Amides.
The Journal of organic chemistry, 2019, 84, 10481-10489
4034016 CIFC22 H23 N5 O3 SF d d 255.259; 21.9278; 7.1347
90; 90; 90
8645.2Rémond, Maxime; Zheng, Zheng; Jeanneau, Erwann; Andraud, Chantal; Bretonnière, Yann; Redon, Sébastien
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push-Pull Dipolar Fluorophores.
The Journal of organic chemistry, 2019, 84, 9965-9974
4034017 CIFC46 H39 N3 O SP 1 21/c 122.113; 9.141; 19.164
90; 105.731; 90
3729Rémond, Maxime; Zheng, Zheng; Jeanneau, Erwann; Andraud, Chantal; Bretonnière, Yann; Redon, Sébastien
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push-Pull Dipolar Fluorophores.
The Journal of organic chemistry, 2019, 84, 9965-9974
4034018 CIFC35 H27 N3 O SP b c a11.1584; 15.1108; 33.728
90; 90; 90
5687Rémond, Maxime; Zheng, Zheng; Jeanneau, Erwann; Andraud, Chantal; Bretonnière, Yann; Redon, Sébastien
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push-Pull Dipolar Fluorophores.
The Journal of organic chemistry, 2019, 84, 9965-9974
4034019 CIFC17 H13 N3 O SP 1 21/m 110.406; 6.819; 10.517
90; 102.1; 90
729.69Rémond, Maxime; Zheng, Zheng; Jeanneau, Erwann; Andraud, Chantal; Bretonnière, Yann; Redon, Sébastien
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push-Pull Dipolar Fluorophores.
The Journal of organic chemistry, 2019, 84, 9965-9974
4034020 CIFC46 H39 N3 O3 SP -111.812; 12.9977; 13.5311
65.759; 79.321; 87.886
1859.7Rémond, Maxime; Zheng, Zheng; Jeanneau, Erwann; Andraud, Chantal; Bretonnière, Yann; Redon, Sébastien
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push-Pull Dipolar Fluorophores.
The Journal of organic chemistry, 2019, 84, 9965-9974
4034021 CIFC16 H14 N2 O SP 1 21/c 17.118; 17.3683; 11.5631
90; 94.347; 90
1425.4Rémond, Maxime; Zheng, Zheng; Jeanneau, Erwann; Andraud, Chantal; Bretonnière, Yann; Redon, Sébastien
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push-Pull Dipolar Fluorophores.
The Journal of organic chemistry, 2019, 84, 9965-9974
4034022 CIFC35 H27 N3 O3 SP 1 21/c 122.307; 9.2796; 14.2356
90; 104.766; 90
2849.5Rémond, Maxime; Zheng, Zheng; Jeanneau, Erwann; Andraud, Chantal; Bretonnière, Yann; Redon, Sébastien
4,5,5-Trimethyl-2,5-dihydrofuran-Based Electron-Withdrawing Groups for NIR-Emitting Push-Pull Dipolar Fluorophores.
The Journal of organic chemistry, 2019, 84, 9965-9974
4034023 CIFC27 H25 N O2 SP 1 21/c 112.7314; 23.7964; 7.2381
90; 90.855; 90
2192.6Li, Chen-Long; Yu, Zhi-Xiang
Asymmetric Synthesis of Azepine-Fused Cyclobutanes from Yne-Methylenecyclopropanes Involving Cyclopropanation/C-C Cleavage/Wagner-Meerwein Rearrangement and Reaction Mechanism.
The Journal of organic chemistry, 2019, 84, 9913-9928
4034024 CIFC27 H24 Br N O2 SP 21 21 217.0599; 15.7538; 20.8421
90; 90; 90
2318.06Li, Chen-Long; Yu, Zhi-Xiang
Asymmetric Synthesis of Azepine-Fused Cyclobutanes from Yne-Methylenecyclopropanes Involving Cyclopropanation/C-C Cleavage/Wagner-Meerwein Rearrangement and Reaction Mechanism.
The Journal of organic chemistry, 2019, 84, 9913-9928

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