Crystallography Open Database

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4037628 CIFC91 H105.5 Cl1.5 N8 Si4P -112.6965; 17.3542; 19.577
78.42; 87.087; 80.742
4169.9Zhao, Kexiang; Long, Guankui; Liu, Wenbo; Li, Dong-Sheng; Gao, Weibo; Zhang, Qichun
U-Shaped Helical Azaarenes: Synthesis, Structures, and Properties.
The Journal of organic chemistry, 2020, 85, 291-295
4037629 CIFC78 H98 N4 Si4P -115.2399; 16.3922; 17.7725
101.974; 113.986; 106.368
3619.9Zhao, Kexiang; Long, Guankui; Liu, Wenbo; Li, Dong-Sheng; Gao, Weibo; Zhang, Qichun
U-Shaped Helical Azaarenes: Synthesis, Structures, and Properties.
The Journal of organic chemistry, 2020, 85, 291-295
4037630 CIFC70 H94 N4 Si4P 1 21/c 112.4305; 25.215; 21.1193
90; 93.47; 90
6607.4Zhao, Kexiang; Long, Guankui; Liu, Wenbo; Li, Dong-Sheng; Gao, Weibo; Zhang, Qichun
U-Shaped Helical Azaarenes: Synthesis, Structures, and Properties.
The Journal of organic chemistry, 2020, 85, 291-295
4037717 CIFC143 H121 Cl2 O13P 1 21 113.575; 20.2391; 20.8569
90; 90.607; 90
5730Nejedlý, Jindřich; Šámal, Michal; Rybáček, Jiří; Sánchez, Isabel Gay; Houska, Václav; Warzecha, Tomáš; Vacek, Jaroslav; Sieger, Ladislav; Buděšínský, Miloš; Bednárová, Lucie; Fiedler, Pavel; Císařová, Ivana; Starý, Ivo; Stará, Irena G
Synthesis of Racemic, Diastereopure, and Enantiopure Carba- or Oxa[5]-, [6]-, [7]-, and -[19]helicene (Di)thiol Derivatives.
The Journal of organic chemistry, 2020, 85, 248-276
4037718 CIFC26 H18 O2 S2P 1 21/c 121.4937; 9.3227; 21.3572
90; 104.637; 90
4140.7Nejedlý, Jindřich; Šámal, Michal; Rybáček, Jiří; Sánchez, Isabel Gay; Houska, Václav; Warzecha, Tomáš; Vacek, Jaroslav; Sieger, Ladislav; Buděšínský, Miloš; Bednárová, Lucie; Fiedler, Pavel; Císařová, Ivana; Starý, Ivo; Stará, Irena G
Synthesis of Racemic, Diastereopure, and Enantiopure Carba- or Oxa[5]-, [6]-, [7]-, and -[19]helicene (Di)thiol Derivatives.
The Journal of organic chemistry, 2020, 85, 248-276
4038011 CIFC51 H68 Cl3 N O8P -110.0957; 16.5247; 16.6164
73.814; 74.718; 89.583
2561.5Smith, Jordan N.; Brind, Thomasin K.; Petrie, Simon B.; Grant, Mikaela S.; Lucas, Nigel T.
One-Step Synthesis of <i>C</i><sub>2v</sub>-Symmetric Resorcin[4]arene Tetraethers.
The Journal of organic chemistry, 2020, 85, 4574-4580
4038012 CIFC60.5 H90 O8.5P -115.8596; 18.1191; 20.983
101.411; 95.612; 107.98
5539.7Smith, Jordan N.; Brind, Thomasin K.; Petrie, Simon B.; Grant, Mikaela S.; Lucas, Nigel T.
One-Step Synthesis of <i>C</i><sub>2v</sub>-Symmetric Resorcin[4]arene Tetraethers.
The Journal of organic chemistry, 2020, 85, 4574-4580
4038013 CIFC78 H121 Br2 Cl5 O8P -111.605; 17.8076; 20.157
83.974; 77.65; 75.603
3935.5Smith, Jordan N.; Brind, Thomasin K.; Petrie, Simon B.; Grant, Mikaela S.; Lucas, Nigel T.
One-Step Synthesis of <i>C</i><sub>2v</sub>-Symmetric Resorcin[4]arene Tetraethers.
The Journal of organic chemistry, 2020, 85, 4574-4580
4038014 CIFC56 H72 O8P 1 21/m 112.5156; 18.1763; 13.11
90; 94.555; 90
2972.94Smith, Jordan N.; Brind, Thomasin K.; Petrie, Simon B.; Grant, Mikaela S.; Lucas, Nigel T.
One-Step Synthesis of <i>C</i><sub>2v</sub>-Symmetric Resorcin[4]arene Tetraethers.
The Journal of organic chemistry, 2020, 85, 4574-4580
4038018 CIFC21 H13 NP 1 21/c 112.2331; 8.2123; 14.7327
90; 105.743; 90
1424.55Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038019 CIFC21 H13 NP 1 21/n 113.1743; 8.2226; 13.5
90; 111.313; 90
1362.4Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038020 CIFC21 H13 NP 1 21/n 113.194; 8.3516; 13.506
90; 110.722; 90
1392Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038021 CIFC21 H13 NP 1 21/c 14.623; 22.358; 13.545
90; 96.486; 90
1391.1Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038022 CIFC21 H13 NP 1 21/c 117.0774; 3.9635; 59.803
90; 90.802; 90
4047.4Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038023 CIFC13 H8 NP 1 21/c 19.3677; 8.1391; 11.6155
90; 99.766; 90
872.79Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038024 CIFC13 H8 NP 1 21/c 111.0286; 5.467; 13.9855
90; 91.742; 90
842.84Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038025 CIFC26 H16 N2P 1 21/c 110.979; 5.4664; 13.966
90; 91.652; 90
837.8Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038026 CIFC26 H16 N2P 1 21/n 13.7918; 9.006; 24.601
90; 90.484; 90
840.1Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038027 CIFC13 H8 NP 1 21/n 15.589; 20.882; 7.697
90; 103.696; 90
872.8Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038028 CIFC13 H8 NC 1 2/c 112.53; 10.289; 13.803
90; 104.918; 90
1719.5Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038029 CIFC26 H16 N2P 1 21/c 112.2463; 30.2305; 9.5734
90; 95.933; 90
3525.2Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038030 CIFC26 H16 N2P 1 21/c 112.305; 30.386; 9.6833
90; 96.608; 90
3596.5Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038031 CIFC34 H32 N2P -19.6837; 12.097; 12.2653
89.133; 66.936; 75.404
1273.6Lu, Qing; Kole, Goutam Kumar; Friedrich, Alexandra; Müller-Buschbaum, Klaus; Liu, Zhiqiang; Yu, Xiaoqiang; Marder, Todd B.
Comparison Study of the Site-Effect on Regioisomeric Pyridyl-Pyrene Conjugates: Synthesis, Structures, and Photophysical Properties.
The Journal of organic chemistry, 2020, 85, 4256-4266
4038035 CIFC8 H13 N O4P 21 21 215.312; 11.535; 13.242
90; 90; 90
811.4Hocine, Sofiane; Berger, Gilles; Hanessian, Stephen
Design and Synthesis of Backbone-Fused, Conformationally Constrained Morpholine-Proline Chimeras.
The Journal of organic chemistry, 2020, 85, 4237-4247
4038038 CIFC20 H26 O2P 1 21/n 14.8245; 13.1695; 26.813
90; 90.043; 90
1703.6Igawa, Kazunobu; Kawasaki, Yuuya; Nozaki, Sora; Kokan, Naoto; Tomooka, Katsuhiko
Ozone Oxidation of Silylalkene: Mechanistic Study and Application for the Synthesis of Silacarboxylic Acid Derivatives.
The Journal of organic chemistry, 2020, 85, 4165-4171
4038046 CIFC12 H2 F2 N4C 1 2/m 110.122; 5.827; 8.812
90; 106.72; 90
497.8Liu, En-Chih; Topczewski, Joseph J.
Gram-Scale Synthesis of 2,5-Difluoro-7,7,8,8-tetracyanoquinodimethane (F<sub>2</sub>-TCNQ).
The Journal of organic chemistry, 2020, 85, 4560-4564
4038047 CIFC9 H12 F N O2 SP 1 21/n 15.8237; 8.8525; 19.1618
90; 92.943; 90
986.57Emenike, Bright U.; Dhami, Simran S.
Determining the Ionization Constants of Organic Acids Using Fluorine Gauche Effects.
The Journal of organic chemistry, 2020, 85, 4896-4900
4038052 CIFC20 H15 Cl N3P 1 21 19.2518; 13.2729; 20.695
90; 90.325; 90
2541.3Wang, Jingdong; Liu, Yuxin; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng
Synthesis of 4-Azaindolines Using Phase-Transfer Catalysis via an Intramolecular Mannich Reaction.
The Journal of organic chemistry, 2020, 85, 4047-4057
4038053 CIFC17 H13 F3 N2 O2 SP 21 21 217.532; 9.197; 22.1
90; 90; 90
1531Wang, Wei; Xiong, Wenhui; Wang, Jinping; Wang, Qiu-An; Yang, Wen
Brønsted Acid-Catalyzed Asymmetric Friedel-Crafts Alkylation of Indoles with Benzothiazole-Bearing Trifluoromethyl Ketone Hydrates.
The Journal of organic chemistry, 2020, 85, 4398-4407
4038055 CIFC18 H14 F0 N2 O0P 1 21/c 116.003; 7.6071; 11.779
90; 108.82; 90
1357.3Jia, Chunqi; Wu, Nini; Cai, Xiaofeng; Li, Gang; Zhong, Lei; Zou, Lei; Cui, Xiuling
Ruthenium-Catalyzed <i>meta</i>-Selective C<sub>Ar</sub>-H Bond Formylation of Arenes.
The Journal of organic chemistry, 2020, 85, 4536-4542
4038056 CIFC26 H15 F OP n a 217.789; 10.907; 20.566
90; 90; 90
1747.2Hoenig, 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
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
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
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
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
4038187 CIFC14 H9 N3 O SP b c a11.6638; 7.5007; 27.8059
90; 90; 90
2432.65Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming
Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles.
The Journal of organic chemistry, 2020, 85, 5570-5579
4038188 CIFC24 H20 N4 O3 SP b c a13.0311; 10.4176; 30.827
90; 90; 90
4184.9Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming
Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles.
The Journal of organic chemistry, 2020, 85, 5570-5579
4038189 CIFC12 H13 N3 O S2P 1 21/c 110.0149; 15.6728; 8.2966
90; 102.539; 90
1271.19Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming
Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles.
The Journal of organic chemistry, 2020, 85, 5570-5579
4038190 CIFC24 H26 N4 O3 SeP 1 21/c 111.4655; 12.7451; 15.4702
90; 100.414; 90
2223.4Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming
Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles.
The Journal of organic chemistry, 2020, 85, 5570-5579
4038191 CIFC25 H25 N5 O2P 1 21/c 115.4232; 6.0725; 24.6911
90; 102.638; 90
2256.5Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming
Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles.
The Journal of organic chemistry, 2020, 85, 5570-5579

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