Crystallography Open Database

Result: there are 591 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Organic & biomolecular chemistry' volume of publication is 16

Left arrow Left arrow First | Left arrow Previous 200 | of 3 | Next 200 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1549028 CIFC23 H26 Br2 O2P 21 21 217.5979; 14.0001; 19.629
90; 90; 90		2088Chang, Shirui; Wang, Lei; Lin, Xufeng
Synthesis and application of a new hexamethyl-1,1'-spirobiindane-based chiral bisphosphine (HMSI-PHOS) ligand in asymmetric allylic alkylation.
Organic & biomolecular chemistry, 2018, 16, 2239-2247
1549215 CIFC24 H33 N O4P 1 21/n 118.3692; 13.9179; 18.6682
90; 107.269; 90		4557.6Shehzadi, Syeda Aaliya; Vande Velde, Christophe M. L.; Saeed, Aamer; Abbaspour Tehrani, Kourosch
Synthesis of highly functionalized 1,6-dihydropyridines via the Zn(OTf)<sub>2</sub>-catalyzed three-component cascade reaction of aldimines and two alkynes (IA<sup>2</sup>-coupling).
Organic & biomolecular chemistry, 2018, 16, 3241-3247
1549216 CIFC20 H27 N O2P -111.9792; 12.1131; 13.4962
94.97; 103.881; 109.494		1762.21Shehzadi, Syeda Aaliya; Vande Velde, Christophe M. L.; Saeed, Aamer; Abbaspour Tehrani, Kourosch
Synthesis of highly functionalized 1,6-dihydropyridines via the Zn(OTf)<sub>2</sub>-catalyzed three-component cascade reaction of aldimines and two alkynes (IA<sup>2</sup>-coupling).
Organic & biomolecular chemistry, 2018, 16, 3241-3247
1549217 CIFC32 H27 Cl N2 O2 SC 1 2/c 117.6414; 17.596; 17.5732
90; 103.004; 90		5315.1Bao, Ming; Lu, Wei; Su, Han; Qiu, Lihua; Xu, Xinfang
A convergent formal [4 + 2] cycloaddition of 1,6-diynes and benzyl azides: construction of spiro-polyheterocycles.
Organic & biomolecular chemistry, 2018, 16, 3258-3265
1549221 CIFC24 H18 N2 O2C 1 2/c 121.348; 9.871; 17.745
90; 92.423; 90		3736Kumari, Santosh; Shakoor, S. M. Abdul; Khullar, Sadhika; Mandal, Sanjay K.; Sakhuja, Rajeev
An unprecedented tandem synthesis of fluorescent coumarin-fused pyrimidines via copper-catalyzed cross-dehydrogenative C(sp<sup>3</sup>)-N bond coupling.
Organic & biomolecular chemistry, 2018, 16, 3220-3228
1549719 CIFC24 H19 N O9P 1 21/c 19.662; 15.701; 14.746
90; 94.165; 90		2231.1Mal, Kajal; Naskar, Barnali; Mondal, Animesh; Goswami, Sanchita; Prodhan, Chandraday; Chaudhuri, Keya; Mukhopadhyay, Chhanda
Dihydroindeno[1,2-b]pyrroles: new Al<sup>3+</sup> selective off-on chemosensors for bio-imaging in living HepG2 cells.
Organic & biomolecular chemistry, 2018, 16, 5920-5931
7155930 CIFC38 H41 N5 O8P 21 21 2110.8476; 17.322; 37.2345
90; 90; 90		6996.4Kicsák, Máté; Mándi, Attila; Varga, Szabolcs; Herczeg, Mihály; Batta, Gyula; Bényei, Attila; Borbás, Anikó; Herczegh, Pál
Tricyclanos: conformationally constrained nucleoside analogues with a new heterotricycle obtained from a d-ribofuranose unit.
Organic & biomolecular chemistry, 2018, 16, 393-401
7155949 CIFC15 H10.25 Cl5.88 D0.88 N O3P 1 21/c 111.5591; 13.2129; 12.0726
90; 90.884; 90		1843.6Rajale, Trideep; Sharma, Shikha; Unruh, Daniel K.; Stroud, Daniel A.; Birney, David M.
A pseudopericyclic [3,5]-sigmatropic rearrangement of a coumarin trichloroacetimidate derivative.
Organic & biomolecular chemistry, 2018, 16, 874-879
7155991 CIFC14 H17 N O4P 21 21 216.32903; 8.54815; 23.7167
90; 90; 90		1283.11Osorio-Nieto, Urbano; Vázquez-Amaya, Laura Y; Höpfl, Herbert; Quintero, Leticia; Sartillo-Piscil, Fernando
The direct and highly diastereoselective synthesis of 3,4-epoxy-2-piperidones. Application to the total synthesis and absolute configurational assignment of 3α,4α-epoxy-5β-pipermethystine.
Organic & biomolecular chemistry, 2017, 16, 77-88
7155992 CIFC17 H19 N O5P 1 21 19.66134; 5.45597; 14.8724
90; 93.7727; 90		782.25Osorio-Nieto, Urbano; Vázquez-Amaya, Laura Y; Höpfl, Herbert; Quintero, Leticia; Sartillo-Piscil, Fernando
The direct and highly diastereoselective synthesis of 3,4-epoxy-2-piperidones. Application to the total synthesis and absolute configurational assignment of 3α,4α-epoxy-5β-pipermethystine.
Organic & biomolecular chemistry, 2017, 16, 77-88
7155993 CIFC14 H17 N O4P 21 21 216.38939; 7.59037; 26.8562
90; 90; 90		1302.47Osorio-Nieto, Urbano; Vázquez-Amaya, Laura Y; Höpfl, Herbert; Quintero, Leticia; Sartillo-Piscil, Fernando
The direct and highly diastereoselective synthesis of 3,4-epoxy-2-piperidones. Application to the total synthesis and absolute configurational assignment of 3α,4α-epoxy-5β-pipermethystine.
Organic & biomolecular chemistry, 2017, 16, 77-88
7155995 CIFC19 H19.5 N2.5 O3P -19.7379; 13.134; 14.204
74.4; 79.76; 87.25		1721.9Bellucci, M. C.; Frigerio, M.; Castellano, C.; Meneghetti, F.; Sacchetti, A.; Volonterio, A.
Design, synthesis, and conformational analysis of 3-cyclo-butylcarbamoyl hydantoins as novel hydrogen bond driven universal peptidomimetics.
Organic & biomolecular chemistry, 2018, 16, 521-525
7155996 CIFC24 H34 N4 O5P 1 c 17.7842; 19.387; 8.315
90; 106.96; 90		1200.3Bellucci, M. C.; Frigerio, M.; Castellano, C.; Meneghetti, F.; Sacchetti, A.; Volonterio, A.
Design, synthesis, and conformational analysis of 3-cyclo-butylcarbamoyl hydantoins as novel hydrogen bond driven universal peptidomimetics.
Organic & biomolecular chemistry, 2018, 16, 521-525
7155997 CIFC300 H324 N12R -3 :H24.68; 24.68; 101.978
90; 90; 120		53793Wang, Xinchang; Peng, Pixian; Xuan, Wei; Wang, Yu; Zhuang, Yongbin; Tian, Zhongqun; Cao, Xiaoyu
Narcissistic chiral self-sorting of molecular face-rotating polyhedra.
Organic & biomolecular chemistry, 2017, 16, 34-37
7155998 CIFC252 H324 N12P -327.8827; 27.8827; 25.2681
90; 90; 120		17012.7Wang, Xinchang; Peng, Pixian; Xuan, Wei; Wang, Yu; Zhuang, Yongbin; Tian, Zhongqun; Cao, Xiaoyu
Narcissistic chiral self-sorting of molecular face-rotating polyhedra.
Organic & biomolecular chemistry, 2017, 16, 34-37
7156001 CIFC24 H18 N4 O4 SP 1 c 17.966; 9.708; 13.669
90; 98.158; 90		1046.4Yang, Ying; Hu, Zi-Lin; Li, Ren-Hao; Chen, Yi-Hui; Zhan, Zhuang-Ping
Pyrazole synthesis via a cascade Sonogashira coupling/cyclization of N-propargyl sulfonylhydrazones.
Organic & biomolecular chemistry, 2018, 16, 197-201
7156002 CIFC25 H21 N5 O7P -19.337; 10.612; 13.512
71.627; 81.23; 72.359		1208.4Mondal, Animesh; Naskar, Barnali; Goswami, Sanchita; Prodhan, Chandraday; Chaudhuri, Keya; Mukhopadhyay, Chhanda
I<sub>2</sub> catalyzed access of spiro[indoline-3,4'-pyridine] appended amine dyad: new ON-OFF chemosensors for Cu<sup>2+</sup> and imaging in living cells.
Organic & biomolecular chemistry, 2018, 16, 302-315
7156003 CIFC17 H28 O4 SiP 21 21 217.2037; 10.9197; 23.762
90; 90; 90		1869.2Ojo, O. Stephen; Nardone, Brunello; Musolino, Stefania F.; Neal, Andrew R.; Wilson, Liam; Lebl, Tomas; Slawin, Alexandra M. Z.; Cordes, David B.; Taylor, James E.; Naismith, James H.; Smith, Andrew D.; Westwood, Nicholas J.
Synthesis of the natural product descurainolide and cyclic peptides from lignin-derived aromatics.
Organic & biomolecular chemistry, 2018, 16, 266-273
7156004 CIFC13 H16 O5P 1 21 114.9553; 8.63515; 19.7885
90; 111.869; 90		2371.61Ojo, O. Stephen; Nardone, Brunello; Musolino, Stefania F.; Neal, Andrew R.; Wilson, Liam; Lebl, Tomas; Slawin, Alexandra M. Z.; Cordes, David B.; Taylor, James E.; Naismith, James H.; Smith, Andrew D.; Westwood, Nicholas J.
Synthesis of the natural product descurainolide and cyclic peptides from lignin-derived aromatics.
Organic & biomolecular chemistry, 2018, 16, 266-273
7156005 CIFC18 H24 O7P 1 21 112.308; 6.22; 13.145
90; 108.591; 90		953.8Ojo, O. Stephen; Nardone, Brunello; Musolino, Stefania F.; Neal, Andrew R.; Wilson, Liam; Lebl, Tomas; Slawin, Alexandra M. Z.; Cordes, David B.; Taylor, James E.; Naismith, James H.; Smith, Andrew D.; Westwood, Nicholas J.
Synthesis of the natural product descurainolide and cyclic peptides from lignin-derived aromatics.
Organic & biomolecular chemistry, 2018, 16, 266-273
7156006 CIFC13 H16 O5P 1 21/c 17.4671; 32.535; 5.2751
90; 108.583; 90		1214.7Ojo, O. Stephen; Nardone, Brunello; Musolino, Stefania F.; Neal, Andrew R.; Wilson, Liam; Lebl, Tomas; Slawin, Alexandra M. Z.; Cordes, David B.; Taylor, James E.; Naismith, James H.; Smith, Andrew D.; Westwood, Nicholas J.
Synthesis of the natural product descurainolide and cyclic peptides from lignin-derived aromatics.
Organic & biomolecular chemistry, 2018, 16, 266-273
7156007 CIFC22 H44 N O7.5 S2.5 SiI 1 2/a 110.1923; 18.865; 31
90; 91.926; 90		5957.2Ojo, O. Stephen; Nardone, Brunello; Musolino, Stefania F.; Neal, Andrew R.; Wilson, Liam; Lebl, Tomas; Slawin, Alexandra M. Z.; Cordes, David B.; Taylor, James E.; Naismith, James H.; Smith, Andrew D.; Westwood, Nicholas J.
Synthesis of the natural product descurainolide and cyclic peptides from lignin-derived aromatics.
Organic & biomolecular chemistry, 2018, 16, 266-273
7156008 CIFC12 H8 I N SP 1 21/a 114.189; 4.122; 19.078
90; 96.17; 90		1109.4Sonawane, Amol D.; Garud, Dinesh R.; Udagawa, Taro; Koketsu, Mamoru
Synthesis of thieno[2,3-b]quinoline and selenopheno[2,3-b]quinoline derivatives via iodocyclization reaction and a DFT mechanistic study.
Organic & biomolecular chemistry, 2018, 16, 245-255
7156009 CIFC24 H20 Br N O2P 21 21 216.6297; 15.443; 20.287
90; 90; 90		2077Guo, Tao; Yuan, Bin-Hua; Liu, Wen-Jie
Highly efficient asymmetric construction of novel indolines and tetrahydroquinoline derivatives via aza-Barbier/C-N coupling reaction.
Organic & biomolecular chemistry, 2017, 16, 57-61
7156010 CIFC25 H22 Br N O2P 1 21 17.297; 10.159; 14.198
90; 97.465; 90		1043.6Guo, Tao; Yuan, Bin-Hua; Liu, Wen-Jie
Highly efficient asymmetric construction of novel indolines and tetrahydroquinoline derivatives via aza-Barbier/C-N coupling reaction.
Organic & biomolecular chemistry, 2017, 16, 57-61
7156011 CIFC22 H28 Br N O2 SP 1 21 118.851; 6.6457; 20.17
90; 114.181; 90		2305.1Guo, Tao; Yuan, Bin-Hua; Liu, Wen-Jie
Highly efficient asymmetric construction of novel indolines and tetrahydroquinoline derivatives via aza-Barbier/C-N coupling reaction.
Organic & biomolecular chemistry, 2017, 16, 57-61
7156012 CIFC20 H20 O3P b c a19.6052; 6.8504; 24.8223
90; 90; 90		3333.7Lombard, Fanny J.; Lepage, Romain J.; Schwartz, Brett D.; Johnston, Ryne C.; Healy, Peter C.; Krenske, Elizabeth H.; Coster, Mark J.
Synthesis of spirocyclic orthoesters by 'anomalous' rhodium(ii)-catalysed intramolecular C-H insertions.
Organic & biomolecular chemistry, 2018, 16, 256-261
7156013 CIFC18 H15 N3 OP 21 21 215.5664; 8.8236; 28.6221
90; 90; 90		1405.79Ruvinskaya, Julia O.; Rostovskii, Nikolai V.; Filippov, Ilya P.; Khlebnikov, Alexander F.; Novikov, Mikhail S.
A novel approach to 5H-pyrazino[2,3-b]indoles via annulation of 3-diazoindolin-2-imines with 2H-azirines or 5-alkoxyisoxazoles under Rh(ii) catalysis.
Organic & biomolecular chemistry, 2017, 16, 38-42
7156014 CIFC18 H12 N4 OC 1 2/c 119.3723; 8.7871; 19.497
90; 109.41; 90		3130.3Zhang, Cheng; Dong, Shanliang; Zheng, Yang; He, Ciwang; Chen, Jiaolong; Zhen, Jingsen; Qiu, Lihua; Xu, Xinfang
Synthesis of spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles via divergent, thermally induced tandem cyclization/migration of alkyne-tethered diazo compounds.
Organic & biomolecular chemistry, 2018, 16, 688-692
7156015 CIFC23 H17 N3 O3 SP 1 21/n 15.432; 19.9758; 17.4712
90; 97.033; 90		1881.51Zhang, Cheng; Dong, Shanliang; Zheng, Yang; He, Ciwang; Chen, Jiaolong; Zhen, Jingsen; Qiu, Lihua; Xu, Xinfang
Synthesis of spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles via divergent, thermally induced tandem cyclization/migration of alkyne-tethered diazo compounds.
Organic & biomolecular chemistry, 2018, 16, 688-692
7156016 CIFC52.5 H46 Br Cl Cu N3 O P2P -110.2838; 12.8459; 20.2842
101.537; 91.712; 108.106		2483.3Zhang, Cheng; Dong, Shanliang; Zheng, Yang; He, Ciwang; Chen, Jiaolong; Zhen, Jingsen; Qiu, Lihua; Xu, Xinfang
Synthesis of spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles via divergent, thermally induced tandem cyclization/migration of alkyne-tethered diazo compounds.
Organic & biomolecular chemistry, 2018, 16, 688-692
7156017 CIFC11 H13 N O3 S3P -16.0374; 9.0824; 13.2438
71.46; 88.791; 78.837		674.86Anitha, Mandala; Swamy, K. C. Kumara
Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes.
Organic & biomolecular chemistry, 2018, 16, 402-413
7156018 CIFC22 H28 N O5 P SP 1 21/c 115.4813; 13.2156; 11.737
90; 98.003; 90		2377.94Anitha, Mandala; Swamy, K. C. Kumara
Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes.
Organic & biomolecular chemistry, 2018, 16, 402-413
7156019 CIFC10 H11 N O2 S3P 1 21/c 16.1417; 9.665; 20.803
90; 97.498; 90		1224.3Anitha, Mandala; Swamy, K. C. Kumara
Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes.
Organic & biomolecular chemistry, 2018, 16, 402-413
7156020 CIFC17 H17 Cl N2 O3 S2P 1 21/c 110.9934; 15.541; 10.7812
90; 99.582; 90		1816.3Anitha, Mandala; Swamy, K. C. Kumara
Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes.
Organic & biomolecular chemistry, 2018, 16, 402-413
7156021 CIFC18 H19 Cl N2 O2 S2P 1 21/c 117.218; 7.657; 14.611
90; 103.225; 90		1875.2Anitha, Mandala; Swamy, K. C. Kumara
Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes.
Organic & biomolecular chemistry, 2018, 16, 402-413
7156022 CIFC33 H55 Cl6 N5 O8P 21 21 2110.1637; 17.2472; 25.5023
90; 90; 90		4470.4Lee, Jaeyeon; Shim, Jihyun; Kang, Philjae; Choi, Moon-Gun; Choi, Soo Hyuk
Side chain-specific 11/9-helix propensity of α/β-peptides with alternating residue types.
Organic & biomolecular chemistry, 2018, 16, 433-438
7156023 CIFC18 H16 N2 O3P -18.2376; 8.7359; 11.8649
98.745; 102.654; 102.432		795.58Samanta, Sadhanendu; Mondal, Susmita; Hajra, Alakananda
A convergent synthesis of vinyloxyimidazopyridine via Cu(i)-catalyzed three-component coupling.
Organic & biomolecular chemistry, 2018, 16, 1088-1092
7156024 CIFC23 H20 N2 OP -19.5942; 9.7522; 10.4775
101.242; 98.692; 100.998		925.62Samanta, Sadhanendu; Mondal, Susmita; Hajra, Alakananda
A convergent synthesis of vinyloxyimidazopyridine via Cu(i)-catalyzed three-component coupling.
Organic & biomolecular chemistry, 2018, 16, 1088-1092
7156025 CIFC13 H14 F N OP b c a11.0397; 10.6042; 19.2081
90; 90; 90		2248.64Maslivetc, Vladimir; Barrett, Colby; Aksenov, Nicolai A.; Rubina, Marina; Rubin, Michael
Intramolecular nucleophilic addition of carbanions generated from N-benzylamides to cyclopropenes.
Organic & biomolecular chemistry, 2018, 16, 285-294
7156026 CIFC19 H19 N3 O9 SP 1 21 15.9946; 13.3006; 13.1317
90; 93.111; 90		1045.47Moczulski, Marek; Drelich, Piotr; Albrecht, Łukasz
Bifunctional catalysis in the stereocontrolled synthesis of tetrahydro-1,2-oxazines.
Organic & biomolecular chemistry, 2018, 16, 376-379
7156027 CIFC30 H24 Cl2 O2P 1 21/c 115.2712; 11.6024; 14.692
90; 107.143; 90		2487.51Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich
Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps.
Organic & biomolecular chemistry, 2018, 16, 750-755
7156028 CIFC24 H30 O2P 1 21/c 114.8423; 16.4382; 12.546
90; 97.066; 90		3037.73Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich
Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps.
Organic & biomolecular chemistry, 2018, 16, 750-755
7156029 CIFC30 H26 O2P -18.2432; 10.4558; 13.9905
89.46; 73.266; 88.81		1154.51Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich
Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps.
Organic & biomolecular chemistry, 2018, 16, 750-755
7156030 CIFC30 H24 F2 O2P -18.2454; 10.3667; 14.2973
90.201; 104.558; 90.585		1182.78Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich
Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps.
Organic & biomolecular chemistry, 2018, 16, 750-755
7156031 CIFC30 H24 Cl2 O2P -16.164; 8.847; 12.0067
106.131; 92.963; 101.467		612.44Jagtap, Pratap R.; Císařová, Ivana; Jahn, Ullrich
Bioinspired total synthesis of tetrahydrofuran lignans by tandem nucleophilic addition/redox isomerization/oxidative coupling and cycloetherification reactions as key steps.
Organic & biomolecular chemistry, 2018, 16, 750-755
7156034 CIFC48 H30 F5 N O2C 1 2/c 129.898; 12.7893; 24.928
90; 123.131; 90		7982.2Muthusamy, Sengodagounder; Balasubramani, Alagesan; Suresh, Eringathodi
A BF<sub>3</sub>·Et<sub>2</sub>O catalyzed atom-economical approach to highly substituted indole-3-carbinols from nitrosobenzenes and propargylic alcohols.
Organic & biomolecular chemistry, 2018, 16, 756-764
7156035 CIFC27 H25 Br N O3.5 SP -112.813; 14.49; 16.225
108.147; 98.12; 116.118		2429.6Wang, Shengzheng; Chen, Shuqiang; Guo, Zhongjie; He, Shipeng; Zhang, Fan; Liu, Xueying; Chen, Weiping; Zhang, Shengyong; Sheng, Chunquan
Synthesis of spiro-tetrahydrothiopyran-oxindoles by Michael-aldol cascade reactions: discovery of potential P53-MDM2 inhibitors with good antitumor activity.
Organic & biomolecular chemistry, 2018, 16, 625-634
7156036 CIFC19 H14 Cl N3 OP 1 21/c 112.6542; 6.7364; 18.7735
90; 103.364; 90		1556.99Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter
A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects.
Organic & biomolecular chemistry, 2018, 16, 717-732
7156037 CIFC16 H16 Cl N3 O4 SP -17.2883; 7.8141; 15.5616
78.263; 86.775; 76.922		845.17Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter
A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects.
Organic & biomolecular chemistry, 2018, 16, 717-732
7156038 CIFC20 H15 N3 OC 1 2/c 132.653; 4.8634; 21.787
90; 119.984; 90		2996.8Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter
A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects.
Organic & biomolecular chemistry, 2018, 16, 717-732
7156039 CIFC21 H20 Cl N3 O3 SP 1 21/c 120.255; 7.228; 14.842
90; 107.35; 90		2074Miliutina, Mariia; Janke, Julia; Hassan, Sidra; Zaib, Sumera; Iqbal, Jamshed; Lecka, Joanna; Sévigny, Jean; Villinger, Alexander; Friedrich, Aleksej; Lochbrunner, Stefan; Langer, Peter
A domino reaction of 3-chlorochromones with aminoheterocycles. Synthesis of pyrazolopyridines and benzofuropyridines and their optical and ecto-5'-nucleotidase inhibitory effects.
Organic & biomolecular chemistry, 2018, 16, 717-732
7156040 CIFC23 H20 O3P 1 21/c 114.4555; 5.39; 22.7358
90; 100.038; 90		1744.35Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties.
Organic & biomolecular chemistry, 2018, 16, 480-489
7156041 CIFC24 H20 O4P -16.7449; 11.3462; 12.9292
67.033; 83.287; 88.921		904.39Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties.
Organic & biomolecular chemistry, 2018, 16, 480-489
7156042 CIFC21 H13 I O4P -17.76154; 14.0693; 16.6303
103.626; 100.792; 99.5738		1691.05Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties.
Organic & biomolecular chemistry, 2018, 16, 480-489
7156043 CIFC24 H19 I O4P 1 21/c 112.5028; 9.0127; 17.7036
90; 103.877; 90		1936.69Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties.
Organic & biomolecular chemistry, 2018, 16, 480-489
7156044 CIFC25 H21 I O4P -16.7649; 12.8471; 24.6221
82.354; 86.293; 88.097		2115.77Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties.
Organic & biomolecular chemistry, 2018, 16, 480-489
7156045 CIFC24 H22 O3P 1 21/c 127.2601; 10.403; 26.2305
90; 90.833; 90		7437.8Shoji, Taku; Tanaka, Miwa; Takagaki, Sho; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties.
Organic & biomolecular chemistry, 2018, 16, 480-489
7156046 CIFC14 H23 N O2P 21 21 217.7672; 9.3611; 19.2665
90; 90; 90		1400.86Liu, Yi-Wen; Ma, Rui-Jun; Yan, Jia-Hang; Zhou, Zhu; Wei, Bang-Guo
Asymmetric synthesis of (-)-sedacryptine through a diastereoselective Mannich reaction of N,O-acetals with ketones.
Organic & biomolecular chemistry, 2018, 16, 771-779
7156047 CIFC27 H43 N O4 SiC 1 2 133.616; 7.9053; 11.1852
90; 91.38; 90		2971.5Liu, Yi-Wen; Ma, Rui-Jun; Yan, Jia-Hang; Zhou, Zhu; Wei, Bang-Guo
Asymmetric synthesis of (-)-sedacryptine through a diastereoselective Mannich reaction of N,O-acetals with ketones.
Organic & biomolecular chemistry, 2018, 16, 771-779
7156048 CIFC20 H17 Br O3C 1 2 118.502; 7.545; 14.387
90; 119.633; 90		1745.7Li, Kun; Zhu, Fu-Lin; Liu, Zhen-Ting; Tong, Jing; Hu, Xiang-Ping
Decarboxylation-promoted Pd-catalyzed asymmetric propargylic [3 + 2] annulation for the enantioselective construction of a quaternary stereocenter in 2,3-dihydrofurans.
Organic & biomolecular chemistry, 2018, 16, 742-749
7156049 CIFC12 H16 O2P 1 21/c 115.4159; 16.6808; 17.397
90; 106.212; 90		4295.7Meng, Zhe; Liu, Bo
Total synthesis of five natural eremophilane-type sesquiterpenoids.
Organic & biomolecular chemistry, 2018, 16, 957-962
7156050 CIFC12 H16 O3P -17.3633; 8.6583; 9.2145
95.128; 98.931; 111.272		533.98Meng, Zhe; Liu, Bo
Total synthesis of five natural eremophilane-type sesquiterpenoids.
Organic & biomolecular chemistry, 2018, 16, 957-962
7156051 CIFC14 H20 O4P 1 21/c 115.0329; 7.9949; 11.4441
90; 97.344; 90		1364.14Meng, Zhe; Liu, Bo
Total synthesis of five natural eremophilane-type sesquiterpenoids.
Organic & biomolecular chemistry, 2018, 16, 957-962
7156052 CIFC54 H60 N4 O8P 21 21 2110.7257; 11.3249; 39.4835
90; 90; 90		4795.96Grajewski, J.; Piotrowska, K.; Zgorzelak, M.; Janiak, A.; Biniek-Antosiak, K; Rychlewska, U.; Gawronski, J.
Introduction of axial chirality at a spiro carbon atom in the synthesis of pentaerythritol-imine macrocycles.
Organic & biomolecular chemistry, 2018, 16, 981-987
7156053 CIFC28 H26 N2 O4P 1 21/n 111.2591; 10.2596; 19.9617
90; 91.988; 90		2304.5Shang, Xinye; Liu, Kun; Zhang, Zhongyin; Xu, Xianhong; Li, Pengfei; Li, Wenjun
Direct access to spirobiisoxazoline via the double 1,3-dipolar cycloaddition of nitrile oxide with allenoate.
Organic & biomolecular chemistry, 2018, 16, 895-898
7156054 CIFC31 H23 Br F N3 O4P 21 21 219.608; 9.984; 28.09
90; 90; 90		2695Wu, Shiqi; Zhu, Guodong; Wei, Shiqiang; Chen, Hongbo; Qu, Jingping; Wang, Baomin
Organocatalytic [3 + 2] cycloaddition of oxindole-based azomethine ylides with 3-nitrochromenes: a facile approach to enantioenriched polycyclic spirooxindole-chromane adducts.
Organic & biomolecular chemistry, 2018, 16, 807-815
7156055 CIFC43 H47 B N2 O3P 21 21 219.6421; 18.6118; 20.0924
90; 90; 90		3605.7Setner, B.; Wierzbicka, M.; Jerzykiewicz, L.; Lisowski, M.; Szewczuk, Z.
The unexpected racemization and hydrogen-deuterium exchange of the hydrogen at the α-carbon of proline analogs containing the 5-azoniaspiro[4.4]nonyl-group.
Organic & biomolecular chemistry, 2018, 16, 825-831
7156056 CIFC23 H30 N2 O4 SP 21 21 219.7197; 12.3037; 19.686
90; 90; 90		2354.2Castán, A; Badorrey, R.; Gálvez, J A; López-Ram-de-Víu, P; Díaz-de-Villegas, M D
Michael addition of carbonyl compounds to nitroolefins under the catalysis of new pyrrolidine-based bifunctional organocatalysts.
Organic & biomolecular chemistry, 2018, 16, 924-935
7156057 CIFC24 H20 I N OP b c a14.565; 11.48; 24.047
90; 90; 90		4020.8Liu, Jie-Jie; Huang, Hong-Yan; Cheng, Liang; Liu, Qi; Wang, Dong; Liu, Li
A catalyst-free intermolecular trans-iodoalkylation of alkynes.
Organic & biomolecular chemistry, 2018, 16, 899-903
7156058 CIFC28 H25 N O3P 1 21/c 112.79; 14.85; 12.068
90; 97.127; 90		2274.4Liu, Jie-Jie; Huang, Hong-Yan; Cheng, Liang; Liu, Qi; Wang, Dong; Liu, Li
A catalyst-free intermolecular trans-iodoalkylation of alkynes.
Organic & biomolecular chemistry, 2018, 16, 899-903
7156059 CIFC24 H19 Cl I N OP -19.2532; 9.542; 12.045
82.895; 86.591; 79.419		1036.7Liu, Jie-Jie; Huang, Hong-Yan; Cheng, Liang; Liu, Qi; Wang, Dong; Liu, Li
A catalyst-free intermolecular trans-iodoalkylation of alkynes.
Organic & biomolecular chemistry, 2018, 16, 899-903
7156060 CIFC33 H30 Cl2 N2 O2P 1 21/c 110.69; 28.425; 9.586
90; 111.155; 90		2716.5Liu, Jie-Jie; Huang, Hong-Yan; Cheng, Liang; Liu, Qi; Wang, Dong; Liu, Li
A catalyst-free intermolecular trans-iodoalkylation of alkynes.
Organic & biomolecular chemistry, 2018, 16, 899-903
7156061 CIFC12 H12 Cl2 N2P 1 21/c 113.368; 7.287; 14.142
90; 113.436; 90		1264Chehal, Navneet K.; Budzelaar, Peter H. M.; Hultin, Philip G.
E-Z isomerization in Suzuki cross-couplings of haloenones: ligand effects and evidence for a separate catalytic cycle.
Organic & biomolecular chemistry, 2018, 16, 1134-1143
7156062 CIFC17 H11 Cl O2P 21 21 216.1663; 12.6929; 17.4233
90; 90; 90		1363.7Chehal, Navneet K.; Budzelaar, Peter H. M.; Hultin, Philip G.
E-Z isomerization in Suzuki cross-couplings of haloenones: ligand effects and evidence for a separate catalytic cycle.
Organic & biomolecular chemistry, 2018, 16, 1134-1143
7156063 CIFC17 H11 Cl O2P 1 21 18.087; 6.124; 13.998
90; 91.49; 90		693Chehal, Navneet K.; Budzelaar, Peter H. M.; Hultin, Philip G.
E-Z isomerization in Suzuki cross-couplings of haloenones: ligand effects and evidence for a separate catalytic cycle.
Organic & biomolecular chemistry, 2018, 16, 1134-1143
7156064 CIFC16 H13 Cl O2P b c a8.858; 11.306; 27.121
90; 90; 90		2716.1Chehal, Navneet K.; Budzelaar, Peter H. M.; Hultin, Philip G.
E-Z isomerization in Suzuki cross-couplings of haloenones: ligand effects and evidence for a separate catalytic cycle.
Organic & biomolecular chemistry, 2018, 16, 1134-1143
7156065 CIFC16 H13 Cl OP b c a8.8054; 11.6093; 26.7629
90; 90; 90		2735.8Chehal, Navneet K.; Budzelaar, Peter H. M.; Hultin, Philip G.
E-Z isomerization in Suzuki cross-couplings of haloenones: ligand effects and evidence for a separate catalytic cycle.
Organic & biomolecular chemistry, 2018, 16, 1134-1143
7156066 CIFC16 H13 Cl O2P 1 21/c 114.28; 9.823; 9.912
90; 98.27; 90		1376Chehal, Navneet K.; Budzelaar, Peter H. M.; Hultin, Philip G.
E-Z isomerization in Suzuki cross-couplings of haloenones: ligand effects and evidence for a separate catalytic cycle.
Organic & biomolecular chemistry, 2018, 16, 1134-1143
7156067 CIFC16 H13 Br F N O4P 21 21 229.849; 7.002; 7.688
90; 90; 90		1606.81Huang, Jian Qiang; Nairoukh, Zackaria; Marek, Ilan
Electrophilic fluorination of stereodefined disubstituted silyl ketene hemiaminals en route to tertiary α-fluorinated carbonyl derivatives.
Organic & biomolecular chemistry, 2018, 16, 1079-1082
7156068 CIFC23 H21 N3 O3I 1 2/a 112.091; 12.635; 25.986
90; 92.324; 90		3967Mondal, Amrita; Kundu, Priyanka; Jash, Moumita; Chowdhury, Chinmay
Palladium-catalysed stereoselective synthesis of 4-(diarylmethylidene)-3,4-dihydroisoquinolin-1(2H)-ones: expedient access to 4-substituted isoquinolin-1(2H)-ones and isoquinolines.
Organic & biomolecular chemistry, 2018, 16, 963-980
7156069 CIFC22 H17 N OP 1 21/n 110.117; 13.923; 12.307
90; 99.313; 90		1710.7Mondal, Amrita; Kundu, Priyanka; Jash, Moumita; Chowdhury, Chinmay
Palladium-catalysed stereoselective synthesis of 4-(diarylmethylidene)-3,4-dihydroisoquinolin-1(2H)-ones: expedient access to 4-substituted isoquinolin-1(2H)-ones and isoquinolines.
Organic & biomolecular chemistry, 2018, 16, 963-980
7156070 CIFC22 H17 N OP -16.6454; 8.8659; 15.1694
94.198; 102.08; 102.439		846.86Mondal, Amrita; Kundu, Priyanka; Jash, Moumita; Chowdhury, Chinmay
Palladium-catalysed stereoselective synthesis of 4-(diarylmethylidene)-3,4-dihydroisoquinolin-1(2H)-ones: expedient access to 4-substituted isoquinolin-1(2H)-ones and isoquinolines.
Organic & biomolecular chemistry, 2018, 16, 963-980
7156071 CIFC24 H17 N O3C 1 2/c 120.649; 10.8202; 20.1324
90; 126.199; 90		3629.8Mondal, Amrita; Kundu, Priyanka; Jash, Moumita; Chowdhury, Chinmay
Palladium-catalysed stereoselective synthesis of 4-(diarylmethylidene)-3,4-dihydroisoquinolin-1(2H)-ones: expedient access to 4-substituted isoquinolin-1(2H)-ones and isoquinolines.
Organic & biomolecular chemistry, 2018, 16, 963-980
7156073 CIFC21 H18 F3 N3 O4P n m a14.9764; 6.8786; 19.4161
90; 90; 90		2000.18Utecht, Greta; Fruziński, Andrzej; Jasiński, Marcin
Polysubstituted 3-trifluoromethylpyrazoles: regioselective (3 + 2)-cycloaddition of trifluoroacetonitrile imines with enol ethers and functional group transformations.
Organic & biomolecular chemistry, 2018, 16, 1252-1257
7156074 CIFC13 H13 F3 N2 OP b c a15.5438; 7.15478; 23.2224
90; 90; 90		2582.62Utecht, Greta; Fruziński, Andrzej; Jasiński, Marcin
Polysubstituted 3-trifluoromethylpyrazoles: regioselective (3 + 2)-cycloaddition of trifluoroacetonitrile imines with enol ethers and functional group transformations.
Organic & biomolecular chemistry, 2018, 16, 1252-1257
7156075 CIFC37 H35 Cl N2 O8P 1 21/c 115.05; 15.9438; 15.0274
90; 113.382; 90		3309.8Ren, Hong-Xia; Peng, Lin; Song, Xiang-Jia; Liao, Li-Guo; Zou, Ying; Tian, Fang; Wang, Li-Xin
Effective and diastereoselective preparation of dispiro[cyclopent-3'-ene]bisoxindoles via novel [3 + 2] annulation of isoindigos and MBH carbonates.
Organic & biomolecular chemistry, 2018, 16, 1297-1304
7156076 CIFC20 H13 Cl N2 OP 21 21 216.3278; 13.3923; 18.8088
90; 90; 90		1593.9Kour, Dilpreet; Gupta, Annah; Kapoor, Kamal K.; Gupta, Vivek K.; Rajnikant, ?; Singh, Deepika; Das, Parthasarathi
Iodine-NH<sub>4</sub>OAc mediated regioselective synthesis of 2-aroyl-3-arylimidazo[1,2-a]pyridines from 1,3-diaryl-prop-2-en-1-ones.
Organic & biomolecular chemistry, 2018, 16, 1330-1336
7156077 CIFC12 H16 N2 O8 SP 41 21 28.791; 8.791; 38.3254
90; 90; 90		2961.85Vejlegaard, Kim; Wegeberg, Christina; McKee, Vickie; Wengel, Jesper
Novel conformationally constrained 2'-C-methylribonucleosides: synthesis and incorporation into oligonucleotides.
Organic & biomolecular chemistry, 2018, 16, 1312-1321
7156078 CIFC12 H16 N2 O8 SP 19.0606; 10.3676; 16.4849
82.4953; 85.481; 74.878		1480.49Vejlegaard, Kim; Wegeberg, Christina; McKee, Vickie; Wengel, Jesper
Novel conformationally constrained 2'-C-methylribonucleosides: synthesis and incorporation into oligonucleotides.
Organic & biomolecular chemistry, 2018, 16, 1312-1321
7156079 CIFC13 H16 N2 O5P 1 21 15.9509; 7.1789; 16.121
90; 90.821; 90		688.6Ahn, Yeong-Chan; Fischer, Conrad; van Belkum, Marco J.; Vederas, John C.
PLP-independent racemization: mechanistic and mutational studies of O-ureidoserine racemase (DcsC).
Organic & biomolecular chemistry, 2018, 16, 1126-1133
7156080 CIFC13 H16 N2 O5P 1 21 15.9238; 7.1787; 16.1585
90; 90.8223; 90		687.07Ahn, Yeong-Chan; Fischer, Conrad; van Belkum, Marco J.; Vederas, John C.
PLP-independent racemization: mechanistic and mutational studies of O-ureidoserine racemase (DcsC).
Organic & biomolecular chemistry, 2018, 16, 1126-1133
7156081 CIFC24 H32 N4 O2P 21 21 218.83; 14.378; 17.669
90; 90; 90		2243.2Darapaneni, Chandra Mohan; Kaniraj, Prathap Jeya; Maayan, Galia
Water soluble hydrophobic peptoids via a minor backbone modification.
Organic & biomolecular chemistry, 2018, 16, 1480-1488
7156082 CIFC13 H10 F3 N O3P b c a11.243; 30.552; 7.3019
90; 90; 90		2508.2Zeng, Qin; Zhang, Li; Xiao, Yuanjing; Zhang, Junliang
Divergent access to N-hydroxypyrroles and isoxazoles via the gold(i)- or Brønsted acid-catalysed regioselective cyclization of N-(2-trifluoromethyl-3-alkynyl) oximes.
Organic & biomolecular chemistry, 2018, 16, 1375-1380
7156083 CIFC12 H7 F3 N2 OP 1 2/c 114.0956; 11.3444; 19.9859
90; 134.705; 90		2271.42Zeng, Qin; Zhang, Li; Xiao, Yuanjing; Zhang, Junliang
Divergent access to N-hydroxypyrroles and isoxazoles via the gold(i)- or Brønsted acid-catalysed regioselective cyclization of N-(2-trifluoromethyl-3-alkynyl) oximes.
Organic & biomolecular chemistry, 2018, 16, 1375-1380
7156084 CIFC26 H19 Cl F3 N3P 1 21 111.476; 10.3255; 12.5157
90; 95.523; 90		1476.2Rahman, Abdul; Xie, En; Lin, Xufeng
Organocatalytic asymmetric synthesis of benzazepinoindole derivatives with trifluoromethylated quaternary stereocenters by chiral phosphoric acid catalysts.
Organic & biomolecular chemistry, 2018, 16, 1367-1374
7156085 CIFC16 H20 O4P -17.424; 8.7348; 10.9347
87.855; 80.444; 88.215		698.53Peter, Clovis; Geoffroy, Philippe; Miesch, Michel
Intramolecular Morita-Baylis-Hillman reaction as a strategy for the construction of tricyclic sesquiterpene cores.
Organic & biomolecular chemistry, 2018, 16, 1381-1389
7156086 CIFC16 H20 O4P 1 21/c 110.4839; 13.1593; 21.3419
90; 103.329; 90		2865Peter, Clovis; Geoffroy, Philippe; Miesch, Michel
Intramolecular Morita-Baylis-Hillman reaction as a strategy for the construction of tricyclic sesquiterpene cores.
Organic & biomolecular chemistry, 2018, 16, 1381-1389
7156087 CIFC16 H10 Cl F N2 OP -17.6576; 10.1949; 10.3237
115.042; 92.445; 108.132		679.55Zhang, Yingchao; Wen, Chunxia; Li, Jizhen
C5-Regioselective C-H fluorination of 8-aminoquinoline amides and sulfonamides with Selectfluor under metal-free conditions.
Organic & biomolecular chemistry, 2018, 16, 1912-1920
7156088 CIFC32 H28 N2 O2P 1 21/n 113.672; 17.459; 23.66
90; 92.451; 90		5642Wan, Ying; Wang, Hai-Qing; Xu, Meng-Meng; Mei, Guang-Jian; Shi, Feng
Direct C3-arylations of 2-indolylmethanols with tryptamines and tryptophols via an umpolung strategy.
Organic & biomolecular chemistry, 2018, 16, 1536-1542
7156089 CIFC36 H35 N3 O2C 1 c 114.9636; 12.2439; 33.362
90; 96.5; 90		6073.1Wan, Ying; Wang, Hai-Qing; Xu, Meng-Meng; Mei, Guang-Jian; Shi, Feng
Direct C3-arylations of 2-indolylmethanols with tryptamines and tryptophols via an umpolung strategy.
Organic & biomolecular chemistry, 2018, 16, 1536-1542
7156090 CIFC13 H12 F3 N O2P 1 21/c 17.8606; 8.5158; 18.6068
90; 98.771; 90		1230.96Achary, Raghavendra; Mathi, Gangadhar Rao; Kim, Seulgi; Hwang, Jong Yeon; Kim, Pilho
Grignard-mediated rearrangement of trifluoroacetyl from dihydroisoquinoline enamides to afford tertiary trifluoromethylcarbinols.
Organic & biomolecular chemistry, 2018, 16, 1452-1456
7156091 CIFC15 H15 F3 N2 OP 1 21/n 16.9263; 8.7238; 22.5349
90; 95.292; 90		1355.84Achary, Raghavendra; Mathi, Gangadhar Rao; Kim, Seulgi; Hwang, Jong Yeon; Kim, Pilho
Grignard-mediated rearrangement of trifluoroacetyl from dihydroisoquinoline enamides to afford tertiary trifluoromethylcarbinols.
Organic & biomolecular chemistry, 2018, 16, 1452-1456
7156092 CIFC32 H28 N2P -110.474; 10.511; 13.935
87.432; 75.479; 71.405		1406.6Li, Xiao-Fang; Zhang, Xing-Guo; Hu, Bo-Lun; Zhang, Xiao-Hong
Palladium-catalyzed dimerization of N-aryl propargylamines for the synthesis of 3-vinylquinolines.
Organic & biomolecular chemistry, 2018, 16, 1736-1744
7156093 CIFC26 H21 N OP -19.8683; 10.505; 10.8101
110.935; 95.718; 105.727		983.13Li, Xiao-Fang; Zhang, Xing-Guo; Hu, Bo-Lun; Zhang, Xiao-Hong
Palladium-catalyzed dimerization of N-aryl propargylamines for the synthesis of 3-vinylquinolines.
Organic & biomolecular chemistry, 2018, 16, 1736-1744
7156094 CIFC26 H38 N6 O6 S6C 1 2/c 115.4619; 9.5378; 22.6171
90; 92.5215; 90		3332.2Cholewiak, Agnieszka; Dobrzycki, Łukasz; Jurczak, Janusz; Ulatowski, Filip
Disulphide bond exchange inhibited by air - kinetic and thermodynamic products in a library of macrocyclic cysteine derivatives.
Organic & biomolecular chemistry, 2018, 16, 2411-2420
7156095 CIFC124.4 H156.62 N20 O25.4 S16.2P 21 21 2119.763; 21.594; 33.712
90; 90; 90		14387Cholewiak, Agnieszka; Dobrzycki, Łukasz; Jurczak, Janusz; Ulatowski, Filip
Disulphide bond exchange inhibited by air - kinetic and thermodynamic products in a library of macrocyclic cysteine derivatives.
Organic & biomolecular chemistry, 2018, 16, 2411-2420
7156096 CIFC31 H48 N4 O7P 1 21 112.0777; 21.0362; 14.3712
90; 107.602; 90		3480.3Konda, Maruthi; Jadhav, Rohit G.; Maiti, Sayan; Mobin, Shaikh M.; Kauffmann, Brice; Das, Apurba K.
Understanding the conformational analysis of gababutin based hybrid peptides.
Organic & biomolecular chemistry, 2018, 16, 1728-1735
7156097 CIFC31 H50 N4 O9P 1 21 110.958; 16.851; 18.872
90; 101.84; 90		3410.6Konda, Maruthi; Jadhav, Rohit G.; Maiti, Sayan; Mobin, Shaikh M.; Kauffmann, Brice; Das, Apurba K.
Understanding the conformational analysis of gababutin based hybrid peptides.
Organic & biomolecular chemistry, 2018, 16, 1728-1735
7156098 CIFC112 H199 N16 O28P 1 21 120.8114; 12.8324; 23.6124
90; 100.846; 90		6193.29Konda, Maruthi; Jadhav, Rohit G.; Maiti, Sayan; Mobin, Shaikh M.; Kauffmann, Brice; Das, Apurba K.
Understanding the conformational analysis of gababutin based hybrid peptides.
Organic & biomolecular chemistry, 2018, 16, 1728-1735
7156099 CIFC17 H14 N2 O4 SP 1 21/c 17.6656; 19.475; 10.707
90; 93.755; 90		1595Zeng, Fanxun; Zhang, Letian; Shao, Xusheng; Li, Zhong; Xu, Xiaoyong
Catalyst-free synthesis of thiazolidines via sequential hydrolysis/rearrangement reactions of 5-arylidenethiazolidin-4-ones at room temperature.
Organic & biomolecular chemistry, 2018, 16, 1932-1938
7156100 CIFC25 H22 Co2 O9P -18.576; 9.059; 16.3
81.049; 89.263; 78.661		1226.3Montaña, Ángel M; Ponzano, Stefano; Sanasi, Maria-Filomena; Kociok-Köhn, Gabriele
Synthesis of the 10-oxabicyclo[5.2.1]decane framework present in bioactive natural products.
Organic & biomolecular chemistry, 2018, 16, 1557-1580
7156101 CIFC32 H23 N O2P -18.1795; 11.924; 14.235
108.105; 96.245; 108.712		1215.9Wang, Wenhui; Sun, Jinwei; Hu, Huayou; Liu, Yun
Copper-catalyzed aerobic cyclizations of tetrahydroisoquinolines with bromoketones and alkenes for the synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines.
Organic & biomolecular chemistry, 2018, 16, 1651-1658
7156102 CIFC20 H11 Cl N2 O2P -18.8729; 9.3458; 10.6991
68.971; 88.64; 69.793		772.05Zhang, Yan; Liu, Jian-Quan; Wang, Xiang-Shan
An efficient synthesis of 16H-dibenzo[2,3:6,7][1,4]oxazepino[5,4-b]quinazolin-16-ones via an Ullmann reaction catalyzed by CuI.
Organic & biomolecular chemistry, 2018, 16, 1679-1685
7156103 CIFC23 H13 Cl F3 N3 OP -19.584; 9.866; 11.366
80.384; 84.059; 66.028		967.5Donthiboina, Kavitha; Namballa, Hari Krishna; Shaik, Siddiq Pasha; Nanubolu, Jagadeesh Babu; Shankaraiah, Nagula; Kamal, Ahmed
Iodine promoted dual oxidative C(sp<sup>3</sup>)-H amination of 2-methyl-3-arylquinazolin-4(3H)-ones: a facile route to 1,4-diarylimidazo[1,5-a]quinazolin-5(4H)-ones.
Organic & biomolecular chemistry, 2018, 16, 1720-1727
7156104 CIFC13 H8 F3 N O3 SP -14.7875; 10.5072; 14.2488
71.68; 88.646; 76.869		661.76Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156105 CIFC15 H7 F3 O4 SP 1 21/c 112.2391; 8.0497; 13.6415
90; 91.602; 90		1343.45Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156106 CIFC17 H12 O3 SP 1 21/c 19.0948; 20.0144; 7.8362
90; 106.353; 90		1368.7Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156107 CIFC11 H5 F3 O3 SP -18.0423; 8.0926; 9.4378
68.147; 84.221; 72.377		543.3Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156108 CIFC16 H9 Br O2 SP -17.8595; 7.9836; 12.2941
89.939; 74.827; 68.477		688.73Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156109 CIFC12 H4 F6 O2 S2P 1 21/c 14.6767; 19.3071; 14.5648
90; 97.949; 90		1302.47Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156110 CIFC15 H7 F3 O2 SP -17.4794; 7.9785; 11.9788
95.823; 102.31; 113.691		625.39Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156111 CIFC13 H9 F3 O3 SI 1 2/a 114.5769; 11.1576; 31.0437
90; 102.048; 90		4937.8Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156112 CIFC17 H12 O2 SP -17.2227; 8.4064; 12.3348
75.046; 76.516; 66.783		657.64Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156113 CIFC11 H5 F3 O2 SP 1 21/c 119.2151; 7.8797; 7.1525
90; 97.718; 90		1073.14Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156114 CIFC21 H14 O4 SP b c a14.1466; 12.4232; 18.979
90; 90; 90		3335.5Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156115 CIFC20 H20 O5C 1 2 117.823; 6.9975; 27.834
90; 100.799; 90		3409.9Henrion, S.; Macé, A; Vallejos, M. M.; Roisnel, T.; Carboni, B.; Villalgordo, J. M.; Carreaux, F.
Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (-)-nicotlactone B and (-)-galbacin.
Organic & biomolecular chemistry, 2018, 16, 1672-1678
7156116 CIFC17 H14 Cl N O5P 21 21 217.5946; 13.4938; 15.8269
90; 90; 90		1621.94Maity, Rajendra; Pan, Subhas Chandra
Organocatalytic asymmetric Michael/hemiacetalization/acyl transfer reaction of α-nitroketones with o-hydroxycinnamaldehydes: synthesis of 2,4-disubstituted chromans.
Organic & biomolecular chemistry, 2018, 16, 1598-1608
7156117 CIFC55 H56 N4 O12P 1 21/c 121.1; 23.1109; 23.201
90; 112.784; 90		10430.9Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156118 CIFC61 H68 N4 O12P 1 21/n 111.9894; 21.2887; 21.7173
90; 93.3; 90		5533.9Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156119 CIFC63 H68 N6 O12P b c a20.9082; 23.7424; 23.9838
90; 90; 90		11905.8Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156120 CIFC57 H60 N4 O12P -112.346; 19.5371; 22.8661
106.561; 102.458; 97.147		5059.3Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156121 CIFC61 H68 Cl4 N4 O12P -111.0365; 16.7007; 17.2058
93.872; 92.106; 108.051		3002.8Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156122 CIFC59 H64 N4 O12P 1 21/c 111.5406; 19.4516; 23.9649
90; 101.455; 90		5272.56Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156123 CIFC13 H9 F3 O4 SP 1 21/c 113.1925; 13.3019; 7.7183
90; 100.757; 90		1330.6Wang, Yajun; Wu, Rui; Zhao, Shijun; Quan, Zhengjun; Su, Yingpeng; Huo, Congde
Air promoted annulation of thiophenols with alkynes leading to benzothiophenes.
Organic & biomolecular chemistry, 2018, 16, 1667-1671
7156124 CIFC17 H22 O7P 21 21 218.16871; 8.25025; 23.3395
90; 90; 90		1572.94Zhang, Zhan-Xin; Wu, Pei-Qian; Li, Hui-Hong; Qi, Feng-Ming; Fei, Dong-Qing; Hu, Qiao-Ling; Liu, Ying-Hong; Huang, Xiao-Ling
Norcrassin A, a novel C<sub>16</sub> tetranorditerpenoid, and bicrotonol A, an unusual dimeric labdane-type diterpenoid, from the roots of Croton crassifolius.
Organic & biomolecular chemistry, 2018, 16, 1745-1750
7156125 CIFC40 H68 O4C 1 2 123.0565; 6.6594; 26.3805
90; 117.81; 90		3582.7Zhang, Zhan-Xin; Wu, Pei-Qian; Li, Hui-Hong; Qi, Feng-Ming; Fei, Dong-Qing; Hu, Qiao-Ling; Liu, Ying-Hong; Huang, Xiao-Ling
Norcrassin A, a novel C<sub>16</sub> tetranorditerpenoid, and bicrotonol A, an unusual dimeric labdane-type diterpenoid, from the roots of Croton crassifolius.
Organic & biomolecular chemistry, 2018, 16, 1745-1750
7156126 CIFC26 H22 N2 O3P 1 21 110.4093; 6.2017; 15.4242
90; 92.398; 90		994.84Zhu, Yanshuo; Guo, Jia; Jin, Shaojing; Guo, Jiaomei; Bai, Xuguan; Wang, Qilin; Bu, Zhanwei
Construction of bridged cyclic N,O-ketal spirooxindoles through a Michael addition/N,O-ketalization sequence.
Organic & biomolecular chemistry, 2018, 16, 1751-1759
7156127 CIFC93 H88 N8 O19 S4P 111.3575; 12.9479; 15.7889
81.909; 88.938; 72.873		2196.15Wang, Zhen-Hua; You, Yong; Chen, Yong-Zheng; Xu, Xiao-Ying; Yuan, Wei-Cheng
An asymmetric organocatalytic vinylogous Mannich reaction of 3-methyl-5-arylfuran-2(3H)-ones with N-(2-pyridinesulfonyl) imines: enantioselective synthesis of δ-amino γ,γ-disubstituted butenolides.
Organic & biomolecular chemistry, 2018, 16, 1636-1640
7156128 CIFC18 H20 N4 O3P -18.7419; 10.7719; 10.9487
65.802; 70.156; 75.68		877.51Obydennov, D. L.; Khammatova, L. R.; Eltsov, O. S.; Sosnovskikh, V. Y.
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines.
Organic & biomolecular chemistry, 2018, 16, 1692-1707
7156129 CIFC27 H22 N4 O2P 1 c 18.521; 10.998; 23.489
90; 93.24; 90		2197.7Obydennov, D. L.; Khammatova, L. R.; Eltsov, O. S.; Sosnovskikh, V. Y.
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines.
Organic & biomolecular chemistry, 2018, 16, 1692-1707
7156130 CIFC27 H21 Cl N4 O2P -18.803; 10.863; 12.961
84.4; 71.46; 80.99		1159.1Obydennov, D. L.; Khammatova, L. R.; Eltsov, O. S.; Sosnovskikh, V. Y.
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines.
Organic & biomolecular chemistry, 2018, 16, 1692-1707
7156131 CIFC18 H13 N3P 1 21/n 18.9797; 17.5384; 9.3882
90; 108.488; 90		1402.24Guan, Qianqian; Sun, Qi; Wen, Lixian; Zha, Zhenggen; Yang, Yu; Wang, Zhiyong
The synthesis of benzimidazoles via a recycled palladium catalysed hydrogen transfer under mild conditions.
Organic & biomolecular chemistry, 2018, 16, 2088-2096
7156132 CIFC27 H20 Br N O SeP 1 21/n 113.917; 10.417; 16.611
90; 103.506; 90		2341.6Li, Xiwang; He, Pei; Zhou, Hai-Bing; Dong, Chune
One-step pathway to selenoisobenzofuran-1(3H)-imine derivatives through highly selective selenocyclization of olefinic amides with benzeneselenyl chloride.
Organic & biomolecular chemistry, 2018, 16, 2150-2155
7156133 CIFC19 H13 Cl F3 N3 O2P 1 21/n 15.77529; 22.1018; 14.0999
90; 101.182; 90		1765.61Lim, Bumhee; Park, Seunggun; Park, Jae Hyun; Gam, Jongsik; Kim, Sanghee; Yang, Jung Woon; Lee, Jeeyeon
A metal-free and mild approach to 1,3,4-oxadiazol-2(3H)-ones via oxidative C-C bond cleavage using molecular oxygen.
Organic & biomolecular chemistry, 2018, 16, 2105-2113
7156134 CIFC11 H8 Cl N3 O2P -15.781; 8.5176; 11.7466
102.453; 90.5; 98.113		558.69Lim, Bumhee; Park, Seunggun; Park, Jae Hyun; Gam, Jongsik; Kim, Sanghee; Yang, Jung Woon; Lee, Jeeyeon
A metal-free and mild approach to 1,3,4-oxadiazol-2(3H)-ones via oxidative C-C bond cleavage using molecular oxygen.
Organic & biomolecular chemistry, 2018, 16, 2105-2113
7156135 CIFC21 H29 N3 O3P b c a16.772; 9.0637; 25.832
90; 90; 90		3926.9Wang, Hui; Fang, Bin; Zhou, Le; Li, Di; Kong, Lin; Uvdal, Kajsa; Hu, Zhangjun
A reversible and highly selective two-photon fluorescent "on-off-on" probe for biological Cu<sup>2+</sup> detection.
Organic & biomolecular chemistry, 2018, 16, 2264-2268
7156136 CIFC7 H11 N3 OP 1 21 15.5524; 7.337; 9.871
90; 91.581; 90		402Halder, Joydev; Das, Debabrata; Nanda, Samik
A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters.
Organic & biomolecular chemistry, 2018, 16, 2549-2575
7156137 CIFC26 H32 O3 SiP 1 21 110.523; 10.046; 11.683
90; 103.959; 90		1198.6Halder, Joydev; Das, Debabrata; Nanda, Samik
A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters.
Organic & biomolecular chemistry, 2018, 16, 2549-2575
7156138 CIFC25 H33 N3 O2 SiP 1 21 110.558; 39.473; 11.458
90; 90; 90		4775Halder, Joydev; Das, Debabrata; Nanda, Samik
A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters.
Organic & biomolecular chemistry, 2018, 16, 2549-2575
7156139 CIFC27 H34 O3 SiP 21 21 218.2816; 11.7445; 25.888
90; 90; 90		2518Halder, Joydev; Das, Debabrata; Nanda, Samik
A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters.
Organic & biomolecular chemistry, 2018, 16, 2549-2575
7156140 CIFC20 H29 Cl OP 1 21 18.5588; 6.9137; 15.0132
90; 99.591; 90		875.96Kratena, Nicolas; Pilz, Sarah M.; Weil, Matthias; Gmeiner, Günter; Enev, Valentin S.; Gärtner, Peter
Synthesis and structural elucidation of a dehydrochloromethyltestosterone metabolite.
Organic & biomolecular chemistry, 2018, 16, 2508-2521
7156141 CIFC19 H29 Cl O2P 21 21 217.5312; 20.9084; 21.2244
90; 90; 90		3342.1Kratena, Nicolas; Pilz, Sarah M.; Weil, Matthias; Gmeiner, Günter; Enev, Valentin S.; Gärtner, Peter
Synthesis and structural elucidation of a dehydrochloromethyltestosterone metabolite.
Organic & biomolecular chemistry, 2018, 16, 2508-2521
7156142 CIFC26 H45 Cl O2 SiC 1 2 113.2696; 7.0208; 28.171
90; 97.17; 90		2604Kratena, Nicolas; Pilz, Sarah M.; Weil, Matthias; Gmeiner, Günter; Enev, Valentin S.; Gärtner, Peter
Synthesis and structural elucidation of a dehydrochloromethyltestosterone metabolite.
Organic & biomolecular chemistry, 2018, 16, 2508-2521
7156143 CIFC19 H29 Cl O2P 1 21 17.1254; 11.6665; 10.8645
90; 103.497; 90		878.21Kratena, Nicolas; Pilz, Sarah M.; Weil, Matthias; Gmeiner, Günter; Enev, Valentin S.; Gärtner, Peter
Synthesis and structural elucidation of a dehydrochloromethyltestosterone metabolite.
Organic & biomolecular chemistry, 2018, 16, 2508-2521
7156144 CIFC19 H27 Cl O2P 21 21 217.4333; 13.538; 16.411
90; 90; 90		1651.5Kratena, Nicolas; Pilz, Sarah M.; Weil, Matthias; Gmeiner, Günter; Enev, Valentin S.; Gärtner, Peter
Synthesis and structural elucidation of a dehydrochloromethyltestosterone metabolite.
Organic & biomolecular chemistry, 2018, 16, 2508-2521
7156145 CIFC33 H25 O2 PP 21 21 2111.149; 11.921; 18.456
90; 90; 90		2452.9Yin, Yao; Weng, Wei-Zhi; Sun, Jian-Guo; Zhang, Bo
Eosin Y-catalyzed, visible-light-promoted carbophosphinylation of allylic alcohols via a radical neophyl rearrangement.
Organic & biomolecular chemistry, 2018, 16, 2356-2361
7156146 CIFC20 H18 N2 OP 1 21/c 111.586; 15.822; 8.7845
90; 97.997; 90		1594.7Wang, Ting; Qing, Xushun; Dai, Chenlu; Su, Zhenjie; Wang, Cunde
Regioselective construction of 1,3-diaryl tetrahydroindazolones via the three-component reaction of 1,3-cyclohexanediones, β-nitrostyrenes and arylhydrazines.
Organic & biomolecular chemistry, 2018, 16, 2456-2463
7156147 CIFC15 H15 N O3P 1 21/c 112.836; 8.234; 13.79
90; 117.679; 90		1290.7Wang, Ting; Qing, Xushun; Dai, Chenlu; Su, Zhenjie; Wang, Cunde
Regioselective construction of 1,3-diaryl tetrahydroindazolones via the three-component reaction of 1,3-cyclohexanediones, β-nitrostyrenes and arylhydrazines.
Organic & biomolecular chemistry, 2018, 16, 2456-2463
7156148 CIFC17 H14 N2 O SP b c a31.267; 8.132; 22.702
90; 90; 90		5772Wang, Ting; Qing, Xushun; Dai, Chenlu; Su, Zhenjie; Wang, Cunde
Regioselective construction of 1,3-diaryl tetrahydroindazolones via the three-component reaction of 1,3-cyclohexanediones, β-nitrostyrenes and arylhydrazines.
Organic & biomolecular chemistry, 2018, 16, 2456-2463
7156149 CIFC27 H26 O5P 1 21/c 111.9068; 10.5151; 18.2449
90; 108.882; 90		2161.36Ivanov, Konstantin L.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya; Budynina, Ekaterina M.
Donor-acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes.
Organic & biomolecular chemistry, 2018, 16, 3897-3909
7156150 CIFC14 H15 Br O6P 1 21/n 18.0373; 17.6384; 10.4852
90; 97.079; 90		1475.1Ivanov, Konstantin L.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya; Budynina, Ekaterina M.
Donor-acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes.
Organic & biomolecular chemistry, 2018, 16, 3897-3909
7156151 CIFC13 H13 Br O5P -18.4387; 8.5555; 9.4816
97.917; 100.06; 92.556		665.94Ivanov, Konstantin L.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya; Budynina, Ekaterina M.
Donor-acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes.
Organic & biomolecular chemistry, 2018, 16, 3897-3909
7156152 CIFC15 H17 Cl O6P 1 21/c 18.835; 6.916; 24.341
90; 90.48; 90		1487.3Ivanov, Konstantin L.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya; Budynina, Ekaterina M.
Donor-acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes.
Organic & biomolecular chemistry, 2018, 16, 3897-3909
7156153 CIFC13 H13 Cl O5P 1 21/c 19.594; 8.102; 17.944
90; 104.5; 90		1350.4Ivanov, Konstantin L.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya; Budynina, Ekaterina M.
Donor-acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes.
Organic & biomolecular chemistry, 2018, 16, 3897-3909
7156154 CIFC16 H19 Br O7P 1 21/c 19.6172; 18.6822; 10.3451
90; 109.39; 90		1753.28Ivanov, Konstantin L.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya; Budynina, Ekaterina M.
Donor-acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes.
Organic & biomolecular chemistry, 2018, 16, 3897-3909
7156155 CIFC21 H15 N3 O6 SP 1 21 18.2614; 11.369; 10.8661
90; 106.297; 90		979.58K, Nagarjuna Reddy; U, Subhadra; B, Sridhar; B V, Subba Reddy
Ru(ii)-Catalyzed spirocyclization of aryl N-sulfonyl ketimines with aryl isocyanates through an aromatic C-H bond activation.
Organic & biomolecular chemistry, 2018, 16, 2522-2526
7156156 CIFC15 H24 N4 O6 SP -16.5612; 9.2289; 15.5715
95.807; 94.598; 98.71		922.86Matić, Josipa; Nekola, Irena; Višnjevac, Aleksandar; Kobetić, Renata; Martin-Kleiner, Irena; Kralj, Marijeta; Žinić, Biserka
C5-Morpholinomethylation of N1-sulfonylcytosines by a one-pot microwave assisted Mannich reaction.
Organic & biomolecular chemistry, 2018, 16, 2678-2687
7156157 CIFC27 H40 O5P 1 21/c 110.94; 23.899; 10.129
90; 96.474; 90		2631.4Qi, Jifeng; Deng, Ziyang; Huang, Bo; Cui, Sunliang
Metal-free α-alkylation of alcohols with para-quinone methides.
Organic & biomolecular chemistry, 2018, 16, 2762-2767
7156158 CIFC16 H10 F2 O3P -17.0746; 8.499; 10.459
92.779; 104.832; 93.958		605Wang, Rui; Han, Jie; Li, Chenchen; Zhang, Jie; Liang, Yong; Wang, Tao; Zhang, Zunting
One-pot synthesis of 3-fluoroflavones via 1-(2-hydroxyphenyl)-3-phenylpropane-1,3-diones and selectfluor at room temperature.
Organic & biomolecular chemistry, 2018, 16, 2479-2488
7156159 CIFC24 H24 OP -116.3273; 16.8364; 17.1138
89.826; 66.421; 65.168		3835.3Virumbrales, Cintia; Suárez-Pantiga, Samuel; Solas, Marta; Fernández-Rodríguez, Manuel A; Sanz, Roberto
Gold(i)-catalyzed diastereoselective synthesis of 1-α-oxybenzyl-1H-indenes.
Organic & biomolecular chemistry, 2018, 16, 2623-2628
7156160 CIFC16 H26 N2 O7P 21 21 218.5004; 12.8701; 16.4218
90; 90; 90		1796.56Josa-Culleré, Laia; Christensen, Kirsten E.; Moloney, Mark G.
Diastereoselective reduction of the tricarbonyl moiety in bicyclic tetramates giving pyroglutamates.
Organic & biomolecular chemistry, 2018, 16, 2705-2710
7156161 CIFC15 H23 I N2 O6P 21 21 218.5534; 13.2093; 16.1337
90; 90; 90		1822.86Josa-Culleré, Laia; Christensen, Kirsten E.; Moloney, Mark G.
Diastereoselective reduction of the tricarbonyl moiety in bicyclic tetramates giving pyroglutamates.
Organic & biomolecular chemistry, 2018, 16, 2705-2710
7156162 CIFC24 H18 N4 O2P -18.7409; 9.6037; 12.1665
72.299; 87.366; 72.955		929.18Kripalaya Ratheesh, Arya; Sparkes, Hazel A.; Prasad, Karnam Jayarampillai Rajendra
A new strategy for the synthesis of diverse benzo[a]carbazoles via a divergent catalytic Michael reaction.
Organic & biomolecular chemistry, 2018, 16, 2527-2540
7156163 CIFC23 H16 N4 O2P -18.3973; 8.5161; 14.1035
97.848; 104.222; 108.609		900.83Kripalaya Ratheesh, Arya; Sparkes, Hazel A.; Prasad, Karnam Jayarampillai Rajendra
A new strategy for the synthesis of diverse benzo[a]carbazoles via a divergent catalytic Michael reaction.
Organic & biomolecular chemistry, 2018, 16, 2527-2540
7156164 CIFC20 H17 Br O5P 21 21 216.3579; 12.657; 22.518
90; 90; 90		1812.1Shen, Yue; Yang, Peng-Fei; Yang, Gaosheng; Chen, Wen-Long; Chai, Zhuo
Lewis acid-catalyzed enantiospecific [3 + 2] annulations of γ-butyrolactone fused cyclopropanes with aromatic aldehydes: synthesis of chiral furanolignans.
Organic & biomolecular chemistry, 2018, 16, 2688-2696
7156165 CIFC21 H20 O7P 21 21 215.8248; 11.9048; 26.568
90; 90; 90		1842.3Shen, Yue; Yang, Peng-Fei; Yang, Gaosheng; Chen, Wen-Long; Chai, Zhuo
Lewis acid-catalyzed enantiospecific [3 + 2] annulations of γ-butyrolactone fused cyclopropanes with aromatic aldehydes: synthesis of chiral furanolignans.
Organic & biomolecular chemistry, 2018, 16, 2688-2696
7156166 CIFC16 H14 B2 F8 O2 S8P 1 21/n 110.7366; 11.0614; 21.0424
90; 101.46; 90		2449.2Schröder, Hendrik V; Witte, Felix; Gaedke, Marius; Sobottka, Sebastian; Suntrup, Lisa; Hupatz, Henrik; Valkonen, Arto; Paulus, Beate; Rissanen, Kari; Sarkar, Biprajit; Schalley, Christoph A.
An aryl-fused redox-active tetrathiafulvalene with enhanced mixed-valence and radical-cation dimer stabilities.
Organic & biomolecular chemistry, 2018, 16, 2741-2747
7156167 CIFC16 H14 O2 S8P 1 21/c 131.739; 4.5314; 14.5044
90; 101.228; 90		2046.1Schröder, Hendrik V; Witte, Felix; Gaedke, Marius; Sobottka, Sebastian; Suntrup, Lisa; Hupatz, Henrik; Valkonen, Arto; Paulus, Beate; Rissanen, Kari; Sarkar, Biprajit; Schalley, Christoph A.
An aryl-fused redox-active tetrathiafulvalene with enhanced mixed-valence and radical-cation dimer stabilities.
Organic & biomolecular chemistry, 2018, 16, 2741-2747
7156168 CIFC33 H33 Br O4 S SeP 1 21 17.9327; 18.8397; 22.3499
90; 100.199; 90		3287.4Luo, Shilong; Zhang, Nan; Wang, Zhen; Yan, Hailong
Enantioselective addition of selenosulfonates to α,β-unsaturated ketones.
Organic & biomolecular chemistry, 2018, 16, 2893-2901
7156169 CIFC30 H30 N2 O4P -19.795; 10.469; 12.397
87.898; 81.097; 82.861		1246Wani, Imtiyaz Ahmad; Bhattacharyya, Aditya; Sayyad, Masthanvali; Ghorai, Manas K.
Temperature-modulated diastereoselective transformations of 2-vinylindoles to tetrahydrocarbazoles and tetrahydrocycloheptadiindoles.
Organic & biomolecular chemistry, 2018, 16, 2910-2922
7156170 CIFC60 H60 N4 O8P -113.1542; 13.3153; 15.723
103.217; 113.154; 93.739		2427.7Wani, Imtiyaz Ahmad; Bhattacharyya, Aditya; Sayyad, Masthanvali; Ghorai, Manas K.
Temperature-modulated diastereoselective transformations of 2-vinylindoles to tetrahydrocarbazoles and tetrahydrocycloheptadiindoles.
Organic & biomolecular chemistry, 2018, 16, 2910-2922
7156171 CIFC26 H26 N2 O4P -17.581; 10.819; 13.144
89.938; 87.155; 82.887		1068.4Wani, Imtiyaz Ahmad; Bhattacharyya, Aditya; Sayyad, Masthanvali; Ghorai, Manas K.
Temperature-modulated diastereoselective transformations of 2-vinylindoles to tetrahydrocarbazoles and tetrahydrocycloheptadiindoles.
Organic & biomolecular chemistry, 2018, 16, 2910-2922
7156172 CIFC14 H16 Cl N3 O6 SP -17.8621; 10.129; 12.5926
70.829; 76.104; 67.503		867.55Zhou, Minghui; Su, Qin; Addepalli, Yesu; He, Yun; Wang, Zhen
An asymmetric Mannich reaction of α-diazocarbonyl compounds and N-sulfonyl cyclic ketimines catalyzed by complexes generated from chiral and achiral phosphines with gold(i).
Organic & biomolecular chemistry, 2018, 16, 2923-2931
7156173 CIFC21 H20 N2 O5P 1 21/n 18.809; 12.652; 16.37
90; 91.413; 90		1824Mondal, Susmita; Hajra, Alakananda
Ruthenium(ii)-catalyzed remote C-H addition of 8 aminoquinoline amide to activated aldehyde.
Organic & biomolecular chemistry, 2018, 16, 2846-2850
7156174 CIFC26 H25.12 O5 SI 1 2/a 120.187; 12.8111; 19.386
90; 110.362; 90		4700.3Ma, Shanshan; Yu, Aimin; Meng, Xiangtai
Phosphine-catalyzed [4 + 2] annulation of γ-benzyl allenoates: facile synthesis of benzothieno[3,2-b]pyran derivatives.
Organic & biomolecular chemistry, 2018, 16, 2885-2892
7156175 CIFC24 H21 Cl O7 SP -110.8783; 11.1724; 11.9506
103.441; 110.162; 103.53		1245.2Ma, Shanshan; Yu, Aimin; Meng, Xiangtai
Phosphine-catalyzed [4 + 2] annulation of γ-benzyl allenoates: facile synthesis of benzothieno[3,2-b]pyran derivatives.
Organic & biomolecular chemistry, 2018, 16, 2885-2892
7156176 CIFC14 H14 N4 OP 1 21/c 17.753; 14.532; 11.144
90; 98.574; 90		1241.5Tong, Feng; Linares-Mendez, Iamnica J; Han, Yi-Fei; Wisner, James A.; Wang, Hong-Bo
Readily functionalized AAA-DDD triply hydrogen-bonded motifs.
Organic & biomolecular chemistry, 2018, 16, 2947-2954
7156177 CIFC28 H22 N O4 PP 1 21/c 112.3199; 22.2918; 9.1023
90; 108.63; 90		2368.8Su, Xiaoxue; Yang, Fan; Wu, Yusheng; Wu, Yangjie
Direct C4-H phosphonation of 8-hydroxyquinoline derivatives employing photoredox catalysis and silver catalysis.
Organic & biomolecular chemistry, 2018, 16, 2753-2756
7156178 CIFC25 H27 F3 N4 O6P -19.0578; 9.3785; 15.7048
103.167; 101.337; 91.84		1269.54Vorobyeva, Daria V.; Vinogradov, Mikhail M.; Nelyubina, Yulia V.; Loginov, Dmitry A.; Peregudov, Alexander S.; Osipov, Sergey N.
Rhodium(iii)-catalyzed CF<sub>3</sub>-carbenoid C-H functionalization of 6-arylpurines.
Organic & biomolecular chemistry, 2018, 16, 2966-2974
7156179 CIFC21 H24 N4 O4P 1 21/n 19.7486; 10.5135; 19.312
90; 100.75; 90		1944.6Vorobyeva, Daria V.; Vinogradov, Mikhail M.; Nelyubina, Yulia V.; Loginov, Dmitry A.; Peregudov, Alexander S.; Osipov, Sergey N.
Rhodium(iii)-catalyzed CF<sub>3</sub>-carbenoid C-H functionalization of 6-arylpurines.
Organic & biomolecular chemistry, 2018, 16, 2966-2974
7156180 CIFC32 H22 Br Cl4 N O2 S2P 1 21/c 19.9316; 9.6118; 33.373
90; 97.634; 90		3157.6Bi, Cheng; Zhang, Lianpeng; Qiu, Guanyinsheng; Li, Xiaofang; Yao, Jinzhong; Zhou, Hongwei
Stereoselective and regioselective 5-exo-dig cyclization of 8-alkynylnaphthalen-1-amines for the synthesis of (E)-2-(arylthio)alkylene-1,2-dihydrobenzo[cd]indoles.
Organic & biomolecular chemistry, 2018, 16, 3006-3011
7156181 CIFC15 H14 N2 OP 1 21/c 110.5352; 5.659; 20.7179
90; 95.495; 90		1229.5Das, Ranajit; Banerjee, Mainak; Rai, Rakesh Kumar; Karri, Ramesh; Roy, Gouriprasanna
Metal-free C(sp<sup>2</sup>)-H functionalization of azoles: K<sub>2</sub>CO<sub>3</sub>/I<sub>2</sub>-mediated oxidation, imination, and amination.
Organic & biomolecular chemistry, 2018, 16, 4243-4260
7156182 CIFC11 H12 I2 N2P -110.1088; 10.1122; 15.6369
106.118; 90.862; 117.901		1337.2Das, Ranajit; Banerjee, Mainak; Rai, Rakesh Kumar; Karri, Ramesh; Roy, Gouriprasanna
Metal-free C(sp<sup>2</sup>)-H functionalization of azoles: K<sub>2</sub>CO<sub>3</sub>/I<sub>2</sub>-mediated oxidation, imination, and amination.
Organic & biomolecular chemistry, 2018, 16, 4243-4260
7156183 CIFC10 H9 I N2P 21 21 218.7463; 9.1092; 13.1444
90; 90; 90		1047.24Das, Ranajit; Banerjee, Mainak; Rai, Rakesh Kumar; Karri, Ramesh; Roy, Gouriprasanna
Metal-free C(sp<sup>2</sup>)-H functionalization of azoles: K<sub>2</sub>CO<sub>3</sub>/I<sub>2</sub>-mediated oxidation, imination, and amination.
Organic & biomolecular chemistry, 2018, 16, 4243-4260
7156184 CIFC11 H12 N2 O3P 1 21/c 14.6419; 24.9757; 9.3367
90; 97.371; 90		1073.5Das, Ranajit; Banerjee, Mainak; Rai, Rakesh Kumar; Karri, Ramesh; Roy, Gouriprasanna
Metal-free C(sp<sup>2</sup>)-H functionalization of azoles: K<sub>2</sub>CO<sub>3</sub>/I<sub>2</sub>-mediated oxidation, imination, and amination.
Organic & biomolecular chemistry, 2018, 16, 4243-4260
7156185 CIFC10 H13 Br N2 OP 1 21/n 18.9971; 8.2161; 14.939
90; 92.864; 90		1102.93Das, Ranajit; Banerjee, Mainak; Rai, Rakesh Kumar; Karri, Ramesh; Roy, Gouriprasanna
Metal-free C(sp<sup>2</sup>)-H functionalization of azoles: K<sub>2</sub>CO<sub>3</sub>/I<sub>2</sub>-mediated oxidation, imination, and amination.
Organic & biomolecular chemistry, 2018, 16, 4243-4260
7156186 CIFC21 H14 Cl N3 OP 1 21/n 15.07; 20.668; 16
90; 93.39; 90		1674Das, Ranajit; Banerjee, Mainak; Rai, Rakesh Kumar; Karri, Ramesh; Roy, Gouriprasanna
Metal-free C(sp<sup>2</sup>)-H functionalization of azoles: K<sub>2</sub>CO<sub>3</sub>/I<sub>2</sub>-mediated oxidation, imination, and amination.
Organic & biomolecular chemistry, 2018, 16, 4243-4260
7156187 CIFC14 H18 N2 O5 SP 1 21/c 110.0967; 11.1751; 13.81
90; 104.85; 90		1506.16Fegheh-Hassanpour, Younes; Ebrahim, Faisal; Arif, Tanzeel; Sintim, Herman O.; Claridge, Timothy D. W.; Amin, Nader T.; Hodgson, David M.
On the ozonolysis of unsaturated tosylhydrazones as a direct approach to diazocarbonyl compounds.
Organic & biomolecular chemistry, 2018, 16, 2876-2884
7156188 CIFC14 H16 F5 N O2 SP 1 21/c 113.9735; 11.3828; 10.4133
90; 109.645; 90		1559.91Savoie, Paul R.; von Hahmann, Cortney N.; Penger, Alexander; Wei, Zheng; Welch, John T.
The control of stereochemistry by the pentafluorosulfanyl group.
Organic & biomolecular chemistry, 2018, 16, 3151-3159

Left arrow Left arrow First | Left arrow Previous 200 | of 3 | Next 200 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.