Crystallography Open Database

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4038057 CIFC26 H15 F SP 1 21/c 112.8863; 18.6245; 7.636
90; 97.048; 90
1818.8Hoenig, Samuel M.; Yan, Youmian; Dougherty, Emily A.; Hudson, Reuben; Petovic, Sava; Lee, Christopher K.; Hu, Yusheng; Gomez, Lucas S.; Katz, Jeffrey L.
Convergent Strategy for the Synthesis of Oxa-, Thia-, and Selena[5]helicenes by Acetylene-Activated S<sub>N</sub>Ar Reactions.
The Journal of organic chemistry, 2020, 85, 4553-4559
4038058 CIFC27 H26 Fe N O PP 18.068; 8.1779; 9.016
74.336; 74.502; 87.802
551.58Arthurs, Ross A.; Hughes, David L.; Richards, Christopher John
Stereoselective Synthesis of all Possible Phosferrox Ligand Diastereoisomers Displaying Three Elements of Chirality: Stereochemical Optimization for Asymmetric Catalysis.
The Journal of organic chemistry, 2020
4038059 CIFC29 H30 Fe N O PP 418.22498; 8.22498; 36.194
90; 90; 90
2448.53Arthurs, Ross A.; Hughes, David L.; Richards, Christopher John
Stereoselective Synthesis of all Possible Phosferrox Ligand Diastereoisomers Displaying Three Elements of Chirality: Stereochemical Optimization for Asymmetric Catalysis.
The Journal of organic chemistry, 2020
4038060 CIFC29 H30 Fe N O PP 21 21 219.2848; 10.9249; 23.5739
90; 90; 90
2391.23Arthurs, Ross A.; Hughes, David L.; Richards, Christopher John
Stereoselective Synthesis of all Possible Phosferrox Ligand Diastereoisomers Displaying Three Elements of Chirality: Stereochemical Optimization for Asymmetric Catalysis.
The Journal of organic chemistry, 2020
4038061 CIFC19 H23 N7 O2 SP n a 2116.5513; 9.6657; 25.6444
90; 90; 90
4102.59Zaķis, Ja Nis Miķelis; Ozols, Kristers; Novosjolova, Irina; Vilšķe Rsts, Reinis; Mishnev, Anatoly; Turks, Ma Ris
Sulfonyl Group Dance: A Tool for the Synthesis of 6-Azido-2-sulfonylpurine Derivatives.
The Journal of organic chemistry, 2020, 85, 4753-4771
4038062 CIFC18 H21 Cl N4 O2 SP -16.2963; 12.2014; 12.3922
89.249; 79.699; 81.512
926.32Zaķis, Ja Nis Miķelis; Ozols, Kristers; Novosjolova, Irina; Vilšķe Rsts, Reinis; Mishnev, Anatoly; Turks, Ma Ris
Sulfonyl Group Dance: A Tool for the Synthesis of 6-Azido-2-sulfonylpurine Derivatives.
The Journal of organic chemistry, 2020, 85, 4753-4771
4038063 CIFC34 H35 F6 N7 O12P 1 21/n 117.907; 9.0483; 25.336
90; 109.74; 90
3863.9Niedbała, Patryk; Majdecki, Maciej; Dąbrowa, Kajetan; Jurczak, Janusz
Selective Carboxylate Recognition Using Urea-Functionalized Unclosed Cryptands: Mild Synthesis and Complexation Studies.
The Journal of organic chemistry, 2020, 85, 5058-5064
4038064 CIFC22 H22 Br N5P 1 21/n 15.7052; 48.2715; 7.5578
90; 106.145; 90
1999.32Kour, Jaspreet; Venkateswarlu, Vunnam; Verma, Praveen K.; Hussain, Yaseen; Dubey, Gurudutt; Bharatam, Prasad V.; Sahoo, Subash C.; Sawant, Sanghapal D.
Oxone-DMSO Triggered Methylene Insertion and C(sp<sup>2</sup>)-C(sp<sup>3</sup>)-H-C(sp<sup>2</sup>) Bond Formation to Access Functional Bis-Heterocycles.
The Journal of organic chemistry, 2020, 85, 4951-4962
4038066 CIFC17 H20 O6P 1 21 18.26368; 7.69518; 12.43341
90; 95.7545; 90
786.662Zang, Yi; Gong, Yihua; Gong, Jiaojiao; Liu, Junjun; Chen, Chunmei; Gu, Lianghu; Zhou, Yuan; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
Fungal Polyketides with Three Distinctive Ring Skeletons from the Fungus <i>Penicillium canescens</i> Uncovered by OSMAC and Molecular Networking Strategies.
The Journal of organic chemistry, 2020, 85, 4973-4980
4038067 CIFC20 H23 O13C 1 2/c 131.4966; 12.8222; 12.3149
90; 109.069; 90
4700.53Zang, Yi; Gong, Yihua; Gong, Jiaojiao; Liu, Junjun; Chen, Chunmei; Gu, Lianghu; Zhou, Yuan; Wang, Jianping; Zhu, Hucheng; Zhang, Yonghui
Fungal Polyketides with Three Distinctive Ring Skeletons from the Fungus <i>Penicillium canescens</i> Uncovered by OSMAC and Molecular Networking Strategies.
The Journal of organic chemistry, 2020, 85, 4973-4980
4038069 CIFC18 H17 N3 O2P b c a13.2254; 7.5242; 30.3701
90; 90; 90
3022.15Bhujanga Rao, Chitturi; Zhang, Ning; Hu, Jiana; Wang, Yu; Liang, Yongjiu; Zhang, Rui; Yuan, Jingwen; Dong, Dewen
Tf<sub>2</sub>O-Mediated Cyclization of α-Acyl-β-(2-aminopyridinyl)acrylamides: Access to N-Substituted 4<i>H</i>-Pyrido[1,2-<i>a</i>]pyrimidin-4-imines.
The Journal of organic chemistry, 2020, 85, 4695-4705
4038070 CIFC27 H25 F N4 O2 SP 1 21/c 115.9019; 15.189; 9.7547
90; 95.855; 90
2343.8De, Pinaki Bhusan; Atta, Sayan; Pradhan, Sourav; Banerjee, Sonbidya; Shah, Tariq A.; Punniyamurthy, Tharmalingam
Cp*Co(III)-Catalyzed C-7 C-C Coupling of Indolines with Aziridines: Merging C-H Activation and Ring Opening.
The Journal of organic chemistry, 2020, 85, 4785-4794
4038071 CIFC4 H10 N8 O8P 1 21/n 17.742; 6.4525; 11.1204
90; 92.759; 90
554.9Lease, Nicholas; Kay, Lisa M.; Brown, Geoffrey W.; Chavez, David E.; Robbins, David; Byrd, Edward F. C.; Imler, Gregory H.; Parrish, Damon A.; Manner, Virginia W.
Synthesis of Erythritol Tetranitrate (ETN) Derivatives: Functional Group Tuning of Explosive Sensitivity.
The Journal of organic chemistry, 2020
4038072 CIFC13 H18 N2 OP 1 21/c 19.6553; 11.4; 11.05
90; 109.035; 90
1149.77Outin, Johanne; Quellier, Pauline; Bélanger, Guillaume
Sequential One-Pot Vilsmeier-Haack and Organocatalyzed Mannich Cyclizations to Functionalized Benzoindolizidines and Benzoquinolizidines.
The Journal of organic chemistry, 2020, 85, 4712-4729
4038073 CIFC16 H21 N O3C 1 2/c 130.3546; 5.078; 20.1975
90; 113.604; 90
2852.8Outin, Johanne; Quellier, Pauline; Bélanger, Guillaume
Sequential One-Pot Vilsmeier-Haack and Organocatalyzed Mannich Cyclizations to Functionalized Benzoindolizidines and Benzoquinolizidines.
The Journal of organic chemistry, 2020, 85, 4712-4729
4038074 CIFC15 H19 N O3P 1 21/n 112.9004; 7.7842; 13.685
90; 104.82; 90
1328.52Outin, Johanne; Quellier, Pauline; Bélanger, Guillaume
Sequential One-Pot Vilsmeier-Haack and Organocatalyzed Mannich Cyclizations to Functionalized Benzoindolizidines and Benzoquinolizidines.
The Journal of organic chemistry, 2020, 85, 4712-4729
4038075 CIFC19 H27 N O3P -19.1272; 9.8101; 19.409
81.582; 82.675; 85.338
1701.63Outin, Johanne; Quellier, Pauline; Bélanger, Guillaume
Sequential One-Pot Vilsmeier-Haack and Organocatalyzed Mannich Cyclizations to Functionalized Benzoindolizidines and Benzoquinolizidines.
The Journal of organic chemistry, 2020, 85, 4712-4729
4038076 CIFC17 H23 N O3P -15.4537; 10.2807; 14.458
71.75; 81.119; 85.2
760.08Outin, Johanne; Quellier, Pauline; Bélanger, Guillaume
Sequential One-Pot Vilsmeier-Haack and Organocatalyzed Mannich Cyclizations to Functionalized Benzoindolizidines and Benzoquinolizidines.
The Journal of organic chemistry, 2020, 85, 4712-4729
4038077 CIFC24 H14 F6 N2 O2P -15.7211; 8.2943; 11.0522
92.866; 91.401; 99.979
515.58Das, Tamal Kanti; Madica, Krishnaprasad; Krishnan, Jagadeesh; Marelli, Udaya Kiran; Biju, Akkattu T.
N-Heterocyclic Carbene Catalysis Exploiting Oxidative Imine Umpolung for the Generation of Imidoyl Azoliums.
The Journal of organic chemistry, 2020, 85, 5114-5121
4038078 CIFC22 H15 N3P c c n11.4534; 27.6502; 9.7523
90; 90; 90
3088.4Yee, Nathan; Dadvand, Afshin; Perepichka, Dmitrii F.
Serendipitous Formation of Semiconducting Semi-Nindigo Indigoid by the Degradation of Diindolopyrrole.
The Journal of organic chemistry, 2020, 85, 5073-5077
4038079 CIFC20 H33 B2 N O4C 1 2/c 112.0036; 24.1961; 15.6222
90; 107.779; 90
4320.6Sarkar, Nabin; Bera, Subhadeep; Nembenna, Sharanappa
Aluminum-Catalyzed Selective Hydroboration of Nitriles and Alkynes: A Multifunctional Catalyst.
The Journal of organic chemistry, 2020, 85, 4999-5009
4038080 CIFC42 H55 Al N5P b c a15.7533; 20.3581; 28.1812
90; 90; 90
9037.9Sarkar, Nabin; Bera, Subhadeep; Nembenna, Sharanappa
Aluminum-Catalyzed Selective Hydroboration of Nitriles and Alkynes: A Multifunctional Catalyst.
The Journal of organic chemistry, 2020, 85, 4999-5009
4038081 CIFC27 H28 N2 O6 SP 1 21 110.0988; 9.9019; 13.2271
90; 97.768; 90
1310.54Han, Pan; Mao, Zhuo-Ya; Li, Ming; Si, Chang-Mei; Wei, Bang-Guo; Lin, Guo-Qiang
Synthesis of Amide Enol Carbamates and Carbonates through Cu(OTf)<sub>2</sub>-Catalyzed Reactions of Ynamides with <i>t</i>-Butyl Carbamates/Carbonates.
The Journal of organic chemistry, 2020, 85, 4740-4752
4038082 CIFC28 H28 Br N2 O5 SP -18.3713; 12.9078; 13.4996
73.9; 73.965; 79.977
1339.4Han, Pan; Mao, Zhuo-Ya; Li, Ming; Si, Chang-Mei; Wei, Bang-Guo; Lin, Guo-Qiang
Synthesis of Amide Enol Carbamates and Carbonates through Cu(OTf)<sub>2</sub>-Catalyzed Reactions of Ynamides with <i>t</i>-Butyl Carbamates/Carbonates.
The Journal of organic chemistry, 2020, 85, 4740-4752
4038083 CIFC56 H88.2 Cl3 F0.9 N8 O9.1P 1 21/n 112.1056; 18.4895; 27.4703
90; 96.269; 90
6111.8Delecluse, Magalie; Colomban, Cédric; Chatelet, Bastien; Chevallier-Michaud, Sabine; Moraleda, Delphine; Dutasta, Jean-Pierre; Martinez, Alexandre
Highly Selective Fluoride Recognition by a Small Tris-Urea Covalent Cage.
The Journal of organic chemistry, 2020, 85, 4706-4711
4038084 CIFC23 H36 O6P 1 21/c 17.3636; 27.079; 11.2689
90; 95.314; 90
2237.3Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038085 CIFC27 H46 O5 SiP -110.142; 11.29; 13.629
83.009; 73.442; 70.541
1409.8Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038086 CIFC27 H42 O7C 1 c 113.152; 16.857; 12.706
90; 107.727; 90
2683.2Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038087 CIFC25 H42 O5 SiP -19.5936; 11.1608; 14.6705
69.414; 79.03; 68.15
1361.7Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038088 CIFC25 H38 O5P 1 21/c 113.878; 17.626; 20.717
90; 97.877; 90
5020Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038089 CIFC25 H40 O5P b c a11.6702; 18.6897; 21.5803
90; 90; 90
4706.93Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038090 CIFC25 H40 O6P 21 21 218.674; 11.5004; 23.904
90; 90; 90
2384.5Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038091 CIFC24 H42 O5 SiP 1 21/c 18.2593; 28.326; 10.769
90; 90.695; 90
2519.3Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038092 CIFC7 H8 O3P b c a8.5906; 7.0884; 20.553
90; 90; 90
1251.5Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038093 CIFC15 H20 O3P 1 21/n 17.8382; 16.7731; 9.7678
90; 101.18; 90
1259.81Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038094 CIFC22 H30 O4P 1 21/c 113.1931; 9.645; 15.711
90; 98.127; 90
1979.11Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038095 CIFC27 H38 N2 O4C 1 2/c 132.983; 19.298; 31.32
90; 98.677; 90
19707Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038096 CIFC7 H12 O3P -15.9092; 7.1583; 9.1902
92.766; 105.442; 108.026
352.68Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038097 CIFC15 H18 O3P 1 21 113.0633; 7.8253; 13.0916
90; 106.413; 90
1283.74Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei
Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol.
The Journal of organic chemistry, 2020, 85, 4813-4837
4038098 CIFC25 H35 F3 O6 SiP 1 21 113.1127; 7.7038; 14.0568
90; 97.859; 90
1406.65Kim, Jae Hyun; Song, Yeonghun; Kim, Min Jung; Kim, Sanghee
Asymmetric Total Synthesis of Inthomycins A, B, and C.
The Journal of organic chemistry, 2020, 85, 4795-4806
4038099 CIFC4 H7 N O2 SP n m a9.7717; 8.6052; 6.3132
90; 90; 90
530.86Blahun, Oleksandr P.; Rozhenko, Alexander B.; Rusanov, Eduard; Zhersh, Serhii; Tolmachev, Andrey A.; Volochnyuk, Dmitriy M.; Grygorenko, Oleksandr O.
Twisting and turning the sulfonamide bond: synthetic, quantum chemical and crystallographic study.
The Journal of organic chemistry, 2020
4038100 CIFC5 H9 N O2 SP 1 21/n 16.4204; 11.0682; 8.9552
90; 96.211; 90
632.64Blahun, Oleksandr P.; Rozhenko, Alexander B.; Rusanov, Eduard; Zhersh, Serhii; Tolmachev, Andrey A.; Volochnyuk, Dmitriy M.; Grygorenko, Oleksandr O.
Twisting and turning the sulfonamide bond: synthetic, quantum chemical and crystallographic study.
The Journal of organic chemistry, 2020
4038101 CIFC4 H9 N O2 SP 1 21/m 15.4761; 8.8259; 6.3408
90; 101.156; 90
300.67Blahun, Oleksandr P.; Rozhenko, Alexander B.; Rusanov, Eduard; Zhersh, Serhii; Tolmachev, Andrey A.; Volochnyuk, Dmitriy M.; Grygorenko, Oleksandr O.
Twisting and turning the sulfonamide bond: synthetic, quantum chemical and crystallographic study.
The Journal of organic chemistry, 2020
4038102 CIFC6 H11 N O2 SP 21 21 216.6488; 9.8314; 11.561
90; 90; 90
755.71Blahun, Oleksandr P.; Rozhenko, Alexander B.; Rusanov, Eduard; Zhersh, Serhii; Tolmachev, Andrey A.; Volochnyuk, Dmitriy M.; Grygorenko, Oleksandr O.
Twisting and turning the sulfonamide bond: synthetic, quantum chemical and crystallographic study.
The Journal of organic chemistry, 2020
4038103 CIFC6 H11 N O2 SC 1 2/c 120.487; 7.8317; 10.8348
90; 121.185; 90
1487.22Blahun, Oleksandr P.; Rozhenko, Alexander B.; Rusanov, Eduard; Zhersh, Serhii; Tolmachev, Andrey A.; Volochnyuk, Dmitriy M.; Grygorenko, Oleksandr O.
Twisting and turning the sulfonamide bond: synthetic, quantum chemical and crystallographic study.
The Journal of organic chemistry, 2020
4038104 CIFC5 H9 N O2 SP 1 21/c 18.0536; 6.891; 11.5341
90; 98.817; 90
632.55Blahun, Oleksandr P.; Rozhenko, Alexander B.; Rusanov, Eduard; Zhersh, Serhii; Tolmachev, Andrey A.; Volochnyuk, Dmitriy M.; Grygorenko, Oleksandr O.
Twisting and turning the sulfonamide bond: synthetic, quantum chemical and crystallographic study.
The Journal of organic chemistry, 2020
4038108 CIFC14 H17 O6 PP 21 21 216.1955; 13.6351; 17.2061
90; 90; 90
1453.51Hernández-Guerra, Daniel; Kennedy, Alan R.; León, Elisa I; Martín, Ángeles; Pérez-Martín, Inés; Rodríguez, María S; Suárez, Ernesto
Synthetic Approaches to Phosphasugars (2-oxo-1,2-oxaphosphacyclanes) Using the Anomeric Alkoxyl Radical β-Fragmentation Reaction as the Key Step.
The Journal of organic chemistry, 2020, 85, 4861-4880
4038109 CIFC24 H19 N OP 1 21/c 112.5295; 6.114; 24.4215
90; 104.339; 90
1812.5Parveen, Naziya; Sekar, Govindasamy
Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones.
The Journal of organic chemistry, 2020, 85, 4682-4694
4038110 CIFC21 H19 N O3C 1 2/c 120.5819; 12.8776; 13.9465
90; 102.536; 90
3608.3Parveen, Naziya; Sekar, Govindasamy
Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones.
The Journal of organic chemistry, 2020, 85, 4682-4694
4038111 CIFC24 H19 N O2P 1 21/n 114.253; 8.2293; 16.3693
90; 98.613; 90
1898.34Parveen, Naziya; Sekar, Govindasamy
Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones.
The Journal of organic chemistry, 2020, 85, 4682-4694
4038112 CIFC23 H15 Cl O2P 1 c 19.7179; 12.4696; 7.5883
90; 106.874; 90
879.95Parveen, Naziya; Sekar, Govindasamy
Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones.
The Journal of organic chemistry, 2020, 85, 4682-4694
4038113 CIFC27 H25 N O4P 1 21/c 18.1334; 31.8582; 9.231
90; 110.33; 90
2242.9Parveen, Naziya; Sekar, Govindasamy
Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones.
The Journal of organic chemistry, 2020, 85, 4682-4694
4038114 CIFC15 H8 O2 S2P 1 21/n 19.424; 9.68; 13.829
90; 94.214; 90
1258.1Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038115 CIFC15 H8 O2 S2P n m a15.3775; 7.2583; 11.0501
90; 90; 90
1233.35Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038116 CIFC13 H8 O2P 1 21/n 19.559; 5.316; 17.355
90; 92.38; 90
881.1Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038117 CIFC13 H6 Cl2 O2C 1 2/m 113.357; 12.364; 7.308
90; 118.676; 90
1058.9Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038118 CIFC15 H8 O4P 1 21/n 19.217; 12.573; 9.542
90; 99.09; 90
1091.9Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038119 CIFC15 H8 O3 SP 1 21/n 19.457; 9.423; 13.368
90; 90.586; 90
1191.2Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038120 CIFC21 H12 O4P 1 21/n 111.825; 17.04; 16.23
90; 109.86; 90
3076Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038121 CIFC23 H12 O4P n a 2117.395; 9.112; 10.203
90; 90; 90
1617.2Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038122 CIFC25 H14 O4P 21 21 2113.845; 13.921; 18.938
90; 90; 90
3650Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038123 CIFC33 H18 O4C 2 2 218.351; 21.414; 13.48
90; 90; 90
2410.6Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038124 CIFC34 H20 Cl2 O4P 21 21 215.3479; 17.257; 28.107
90; 90; 90
2594Wössner, Jan S; Esser, Birgit
Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties.
The Journal of organic chemistry, 2020, 85, 5048-5057
4038125 CIFC132 H204 Cl36 Cu12 N48 O49.66C 1 2/m 126.405; 29.054; 13.1898
90; 105.232; 90
9763.4Yepremyan, Akop; Mekhail, Magy A.; Niebuhr, Brian P.; Pota, Kristof; Sadagopan, Nishanth; Schwartz, Timothy M.; Green, Kayla N.
Synthesis of 12-Membered Tetra-aza Macrocyclic Pyridinophanes Bearing Electron-Withdrawing Groups.
The Journal of organic chemistry, 2020, 85, 4988-4998
4038126 CIFC13 H20 Cl2 F6 N4 O6 S2P 1 21/c 111.471; 7.8357; 24.225
90; 90.475; 90
2177.3Yepremyan, Akop; Mekhail, Magy A.; Niebuhr, Brian P.; Pota, Kristof; Sadagopan, Nishanth; Schwartz, Timothy M.; Green, Kayla N.
Synthesis of 12-Membered Tetra-aza Macrocyclic Pyridinophanes Bearing Electron-Withdrawing Groups.
The Journal of organic chemistry, 2020, 85, 4988-4998
4038127 CIFC17 H21 N O3P -18.3484; 8.596; 10.5662
94.799; 97.856; 97.882
739.98Rinaldi, Antonia; Langé, Vittoria; Scarpi, Dina; Occhiato, Ernesto G.
One-Pot Access to 1,7a-Dihydro-1,3a-ethano-indene and 1,8a-Dihydro-1,3a-ethano-azulene Skeletons by a Sequential Gold(I)-Catalyzed Propargyl Claisen Rearrangement/Nazarov Cyclization/[4+2] Cycloaddition Reaction.
The Journal of organic chemistry, 2020, 85, 5078-5086
4038128 CIFC29 H22 O2P 1 21/c 17.7659; 24.493; 11.05
90; 102.439; 90
2052.48Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038129 CIFC29 H22 S2P 1 21/c 17.63396; 24.8669; 11.3736
90; 102.352; 90
2109.1Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038130 CIFC33 H32 N2I 41/a :230.826; 30.826; 10.4869
90; 90; 90
9965.1Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038131 CIFC25 H12 O S2C 1 2/c 125.198; 8.1409; 17.1786
90; 105.547; 90
3395Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038132 CIFC29 H22 N2 OP 1 21/c 14.8822; 24.2724; 18.1588
90; 111.851; 90
1997.27Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038133 CIFC59 H52 N4 OI -428.0545; 28.0545; 5.2665
90; 90; 90
4145.03Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038134 CIFC118 H99 N9I -428.056; 28.056; 5.2757
90; 90; 90
4152.71Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038135 CIFC61 H54 N4 OI -428.0572; 28.0572; 5.2734
90; 90; 90
4151.25Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek
Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes.
The Journal of organic chemistry, 2020, 85, 4672-4681
4038136 CIFC17 H21 N O3P 21 21 2116.6762; 15.5082; 6.1829
90; 90; 90
1599.01Banjare, Shyam Kumar; Biswal, Pragati; Ravikumar, Ponneri Chandrababu
Cobalt-Catalyzed One-Step Access to Pyroquilon and C-7 Alkenylation of Indoline with Activated Alkenes Using Weakly Coordinating Functional Group.
The Journal of organic chemistry, 2020
4038137 CIFC11 H10 F N OP c a 2115.8646; 5.3549; 10.5519
90; 90; 90
896.42Banjare, Shyam Kumar; Biswal, Pragati; Ravikumar, Ponneri Chandrababu
Cobalt-Catalyzed One-Step Access to Pyroquilon and C-7 Alkenylation of Indoline with Activated Alkenes Using Weakly Coordinating Functional Group.
The Journal of organic chemistry, 2020
4038138 CIFC12 H15 N O4 SP 1 21/n 115.8628; 10.9634; 16.5749
90; 117.617; 90
2554.1Yuan, Yang; Chen, Bo; Zhang, Youcan; Wu, Xiao-Feng
Pd/C-Catalyzed Carbonylative Synthesis of α-Carbonyl-α'-Amide Sulfoxonium Ylides from Azides.
The Journal of organic chemistry, 2020
4038139 CIFC29 H27 N3P 1 n 16.2091; 11.431; 31.863
90; 94.557; 90
2254.4Chang, Meng-Yang; Tsai, Yu-Lin
One-Pot Amberlyst 15-Controlled Cyclocondensation of Piperidines and Arylaldehydes. Synthesis of 3,5-Diarylmethyl Pyridines.
The Journal of organic chemistry, 2020
4038141 CIFC18 H14 Cl N O2P -18.2025; 8.57; 12.1558
99.418; 99.192; 116.633
726.73Li, Zhenmin; Xie, Jianwei; Lu, Ping; Wang, Yanguang
Synthesis of 8-Alkoxy-5H-isochromeno[3,4-c]isoquinolines and 1-Alkoxy-4-arylisoquinolin-3-ols through Rh(III)-Catalyzed C-H Functionalization of Benzimidates with 4-Diazoisochroman-3-imines and 4-Diazoisoquinolin-3-ones.
The Journal of organic chemistry, 2020
4038142 CIFC25 H22 N2 O3 SP 1 21/c 18.1535; 23.0669; 11.4261
90; 96.471; 90
2135.28Li, Zhenmin; Xie, Jianwei; Lu, Ping; Wang, Yanguang
Synthesis of 8-Alkoxy-5H-isochromeno[3,4-c]isoquinolines and 1-Alkoxy-4-arylisoquinolin-3-ols through Rh(III)-Catalyzed C-H Functionalization of Benzimidates with 4-Diazoisochroman-3-imines and 4-Diazoisoquinolin-3-ones.
The Journal of organic chemistry, 2020
4038143 CIFC22 H13 F2 N OP c c n16.8351; 25.1745; 7.294
90; 90; 90
3091.31Li, Zhenmin; Xie, Jianwei; Lu, Ping; Wang, Yanguang
Synthesis of 8-Alkoxy-5H-isochromeno[3,4-c]isoquinolines and 1-Alkoxy-4-arylisoquinolin-3-ols through Rh(III)-Catalyzed C-H Functionalization of Benzimidates with 4-Diazoisochroman-3-imines and 4-Diazoisoquinolin-3-ones.
The Journal of organic chemistry, 2020
4038144 CIFC25 H24 N2 O4 SP -19.1814; 11.0147; 12.5984
80.885; 84.454; 65.767
1146.4Li, Zhenmin; Xie, Jianwei; Lu, Ping; Wang, Yanguang
Synthesis of 8-Alkoxy-5H-isochromeno[3,4-c]isoquinolines and 1-Alkoxy-4-arylisoquinolin-3-ols through Rh(III)-Catalyzed C-H Functionalization of Benzimidates with 4-Diazoisochroman-3-imines and 4-Diazoisoquinolin-3-ones.
The Journal of organic chemistry, 2020
4038145 CIFC16 H10 N2 OP 1 21/n 114.297; 5.3712; 14.656
90; 89.839; 90
1125.5Li, Zhenmin; Xie, Jianwei; Lu, Ping; Wang, Yanguang
Synthesis of 8-Alkoxy-5H-isochromeno[3,4-c]isoquinolines and 1-Alkoxy-4-arylisoquinolin-3-ols through Rh(III)-Catalyzed C-H Functionalization of Benzimidates with 4-Diazoisochroman-3-imines and 4-Diazoisoquinolin-3-ones.
The Journal of organic chemistry, 2020
4038146 CIFC37 H24 OP 1 21/n 110.2162; 14.533; 16.867
90; 97.256; 90
2484.2Mayer, Péter J; El Bakouri, Ouissam; Holczbauer, Tamás; Samu, Gergely F.; Janáky, Csaba; Ottosson, Henrik; London, Gábor
Structure-property relationships in unsymmetric bis(antiaromatics): Who wins the battle between pentalene and benzocyclobutadiene?
The Journal of organic chemistry, 2020
4038147 CIFC49 H50 O8P 1 21 110.5804; 17.897; 12.255
90; 115.276; 90
2098.41Li, Yulong; Xu, Zhezhe; Xie, Zhipeng; Guan, Xingchao; Xie, Zhixiang
Total Synthesis of Nominal <i>ent</i>-Chlorabietol B.
The Journal of organic chemistry, 2020
4038148 CIFC21 H15 N O6C 1 2/c 118.904; 7.2383; 25.7728
90; 96.279; 90
3505.4Noland, Wayland E.; Kumar, Honnaiah Vijay; Reddi, Yernaidu; Cramer, Christopher J.; Novikov, Alexei V.; Kim, Hyejin; Zhu, Yumeng; Chin, Yoke Ching; Zhou, Yuqi; Radakovic, Predrag; Uprety, Anjola; Xie, Jun; Flick, Grant C.
Diels-Alder/Ene Reactivities of 2-(1´-Cycloalkenyl)thiophenes and 2-(1´-Cycloalkenyl)benzo[b]thiophenes with N-Phenylmaleimides: Role of Cycloalkene Ring Size on Benzothiophene and Dibenzothiophene Product Distributions.
The Journal of organic chemistry, 2020
4038149 CIFC30 H24 Br2 N2 O4 SP 21 21 217.6871; 13.649; 25.234
90; 90; 90
2647.6Noland, Wayland E.; Kumar, Honnaiah Vijay; Reddi, Yernaidu; Cramer, Christopher J.; Novikov, Alexei V.; Kim, Hyejin; Zhu, Yumeng; Chin, Yoke Ching; Zhou, Yuqi; Radakovic, Predrag; Uprety, Anjola; Xie, Jun; Flick, Grant C.
Diels-Alder/Ene Reactivities of 2-(1´-Cycloalkenyl)thiophenes and 2-(1´-Cycloalkenyl)benzo[b]thiophenes with N-Phenylmaleimides: Role of Cycloalkene Ring Size on Benzothiophene and Dibenzothiophene Product Distributions.
The Journal of organic chemistry, 2020
4038150 CIFC30 H28 F N O5 SP 1 21/n 111.104; 18.824; 12.741
90; 90.46; 90
2663.1Qu, Yi; Xu, Wentao; Zhang, Jingjing; Liu, Yuxiu; Li, Yongqiang; Song, Hongjian; Wang, Qingmin
Visible-Light-Mediated [2+2+1] Carbocyclization Reactions of 1,7-Enynes with Bromofluoroacetate to Form Fused Monofluorinated Cyclopenta[c]quinolin-4-ones.
The Journal of organic chemistry, 2020
4038151 CIFC29 H26 F N O5 SF d d 256.287; 11.896; 16.142
90; 90; 90
10809Qu, Yi; Xu, Wentao; Zhang, Jingjing; Liu, Yuxiu; Li, Yongqiang; Song, Hongjian; Wang, Qingmin
Visible-Light-Mediated [2+2+1] Carbocyclization Reactions of 1,7-Enynes with Bromofluoroacetate to Form Fused Monofluorinated Cyclopenta[c]quinolin-4-ones.
The Journal of organic chemistry, 2020
4038152 CIFC45 H53 N O8P 1 21/c 111.9373; 17.1695; 19.1617
90; 106.874; 90
3758.2Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038153 CIFC92.6 H116.6 F4.8 N O23.6P -112.4816; 13.6012; 14.6525
64.281; 77.984; 77.832
2171.4Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038154 CIFC300.75 H72 N O13.75P -112.3935; 12.7003; 31.989
79.2; 80.931; 81.646
4849.2Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038155 CIFC102 H126 N2 O23P -112.5897; 12.7023; 15.9641
77.76; 75.988; 73.191
2343.3Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038156 CIFC51 H63 N O10P b c n50.063; 16.205; 16.6954
90; 90; 90
13544.5Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038157 CIFC52 H65 N O10P b c n50.2896; 16.4078; 16.6971
90; 90; 90
13777.5Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038158 CIFC47 H54 O10P -112.1038; 13.3562; 14.1984
68.194; 72.806; 89.471
2022.7Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038159 CIFC7 H6 F3 N O2P 3214.511; 14.511; 10.2
90; 90; 120
1860.1Taimoory, S. Maryamdokht; Twum, Kwaku; Dashti, Mohadeseh; Pan, FangFang; Lahtinen, Manu; Rissanen, Kari; Puttreddy, Rakesh; Trant, John F.; Beyeh, Ngong Kodiah
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three Component Complexes.
The Journal of organic chemistry, 2020
4038160 CIFC14 H12 N4P 1 21/c 116.5911; 5.9508; 12.3528
90; 93.863; 90
1216.82Zhang, Yuan; Lee, Jack Chang Hung; Reese, Matthew R.; Boscoe, Brian P.; Humphrey, John M.; Helal, Christopher J.
5-Aryl Tetrazoles from Direct C-H Arylation with Aryl Bromides.
The Journal of organic chemistry, 2020
4038161 CIFC33 H30 N2 O4 S2P 1 21/c 113.1147; 22.827; 9.7575
90; 98.306; 90
2890.46Watanabe, Kazuhiro; Moriyama, Katsuhiko
C-H Sulfonylation via 1,3-Rearrangement of Sulfonyl Group in N-protected 3-Bissulfonimidoindole Derivatives Using Fluorine Reagent.
The Journal of organic chemistry, 2020
4038162 CIFC22 H20 N2 O4 S2C 1 2/c 132.963; 8.7052; 15.5575
90; 114.78; 90
4053.2Watanabe, Kazuhiro; Moriyama, Katsuhiko
C-H Sulfonylation via 1,3-Rearrangement of Sulfonyl Group in N-protected 3-Bissulfonimidoindole Derivatives Using Fluorine Reagent.
The Journal of organic chemistry, 2020

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