Crystallography Open Database

Result: there are 528485 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

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Displaying all data in COD

Blue left arrow Blue left arrow First | Blue left arrow Previous 500 | of 1057 | Next 500 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
1554761 CIFC22 H19 N3 O4P 1 21/c 18.7562; 23.4732; 8.8632
90; 92.21; 90		1820.35Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554762 CIFC21 H15 Cl F N3 O3P 1 21/c 17.3959; 19.3566; 12.7098
90; 91.147; 90		1819.2Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554763 CIFC29 H19 F6 N3 O4P 1 21/c 115.9357; 13.7866; 11.8725
90; 93.908; 90		2602.3Song, Zehua; Wang, Guotong; Li, Wei; Li, Shengkun
Innate pharmacophore assisted selective C–H functionalization to therapeutically important nicotinamides
Organic Chemistry Frontiers, 2019, 6, 1613
1554764 CIFC25 H20 B F4 N OP 1 21/n 110.72; 18.331; 12.174
90; 110.527; 90		2240.4Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554765 CIFC25 H21 B F4 N2 O2P 1 21/c 112.3471; 13.3272; 13.9786
90; 98.588; 90		2274.42Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong
Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts.
Organic letters, 2015, 17, 924-927
1554766 CIFC60 H78 Cl2 N4 O16P -115.267; 19.087; 24.39
87.94; 83.839; 73.08		6760Jordan, Jacobs H.; Wishard, Anthony; Mague, Joel T.; Gibb, Bruce C.
Binding properties and supramolecular polymerization of a water-soluble resorcin[4]arene
Organic Chemistry Frontiers, 2019, 6, 1236
1554767 CIFC31 H24 Cl N O3P 1 21 17.081; 19.406; 9.491
90; 98.161; 90		1290.99Jayakumar, Samydurai; Kumarswamyreddy, Nandarapu; Prakash, Muthuraj; Kesavan, Venkitasamy
Palladium catalyzed asymmetric allylation of 3-OBoc-oxindoles: an efficient synthesis of 3-allyl-3-hydroxyoxindoles.
Organic letters, 2015, 17, 1066-1069
1554768 CIFC6.21 H2.28 Cl0.48 N0.07 O0.28 S0P -19.9983; 16.3521; 19.4651
102.163; 90.869; 105.091		2995.41Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554769 CIFC143 H54 N2 O10 S2P 1 21/n 110.4701; 25.097; 16.2566
90; 91.218; 90		4270.8Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554770 CIFC70 H22.75 N O4.88 S2C 1 c 114.4203; 27.3088; 10.3569
90; 94.182; 90		4067.7Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554771 CIFC81 H42.7 N O5.85 S2P -110.4366; 16.3952; 16.824
110.869; 99.019; 100.619		2565.14Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554772 CIFC143 H57.4 N2 O11.7 S2P 1 21/n 110.4595; 25.0584; 16.2556
90; 91.316; 90		4259.4Zhang, Hao; Su, Jie; Pan, Changwang; Lu, Xing; Gan, Liangbing
Synthesis of an open-cage fullerene-based unidirectional H-bonding network and its coordination with titanium
Organic Chemistry Frontiers, 2019, 6, 1397
1554773 CIFC49.05 H59.38 Cl5.87 Li0.15 N3 P3 Ti2P -110.3083; 14.3567; 19.2355
75.287; 74.747; 84.913		2655.7Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
1554774 CIFC16 H19 Cl3 N P TiP -18.8951; 9.2936; 13.0036
79.226; 76.069; 64.74		939.24Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J.
Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes.
Organic letters, 2015, 17, 752-755
1554775 CIFC19 H20 N2 SeP 1 21/c 113.3462; 10.2259; 12.0633
90; 96.466; 90		1635.89Guo, Tao; Wei, Xu-Ning; Liu, Yu; Zhang, Pan-Ke; Zhao, Yun-Hui
Oxidative dual C–H selenation of imidazoheterocycles with ethers or alkanes using selenium powder via a radical pathway
Organic Chemistry Frontiers, 2019, 6, 1414
1554776 CIFC35 H26 N1.6 O10P 21 21 2113.871; 15.1622; 64.627
90; 90; 90		13592Cao, Pei; Yang, Jing; Miao, Cui-Ping; Yan, Yijun; Ma, Ya-Tuan; Li, Xiao-Nian; Zhao, Li-Xing; Huang, Sheng-Xiong
New duclauxamide from Penicillium manginii YIM PH30375 and structure revision of the duclauxin family.
Organic letters, 2015, 17, 1146-1149
1554777 CIFC21 H18 N O3 PP 21 21 218.4621; 19.7458; 21.2129
90; 90; 90		3544.5Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554778 CIFC25 H23 N2 O2 PP 1 21/n 118.5757; 6.176; 18.9148
90; 98.809; 90		2144.38Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554779 CIFC22.5 H14.5 Cl1.5 F3 N2 O2 PC 1 2/c 129.394; 6.3419; 28.119
90; 121.188; 90		4484.2Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554780 CIFC21 H15 N2 O2 PC 1 2/c 124.331; 10.2408; 14.54
90; 102.686; 90		3534.5Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554781 CIFC21 H15 N2 O2 PC 1 2/c 126.4131; 9.7872; 14.9148
90; 115.7; 90		3474.22Bard, Jeremy P.; Deng, Chun-Lin; Richardson, Hannah C.; Odulio, Jacob M.; Barker, Joshua E.; Zakharov, Lev N.; Cheong, Paul H.-Y.; Johnson, Darren W.; Haley, Michael M.
Synthesis, photophysical properties, and self-dimerization studies of 2-λ5-phosphaquinolin-2-ones
Organic Chemistry Frontiers, 2019, 6, 1257
1554782 CIFC34 H29 N5 O4 SP -19.7972; 10.509; 15.4371
72.931; 74.564; 84.268		1464.2Du, Zao; Xing, Yanpeng; Lu, Ping; Wang, Yanguang
Copper-catalyzed cascade double C3-indolations of 3-diazoindolin-2-imines with indoles: convenient access to 3,3-diaryl-2-iminoindoles.
Organic letters, 2015, 17, 1192-1195
1554783 CIFC24 H27 N3 O2P 1 21/c 117.5333; 9.245; 13.3467
90; 107.946; 90		2058.18Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
1554784 CIFC13 H18 N2 O2 S2P b c a14.1538; 10.7714; 20.0319
90; 90; 90		3054Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554785 CIFC11 H12 O4 S2P -15.1535; 7.3073; 16.2864
81.694; 82.41; 74.561		582.16Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554786 CIFC36 H38 O2 S2C 1 c 119.6986; 10.9502; 16.5805
90; 122.988; 90		2999.9Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554787 CIFC40 H46 O2 S2P -19.4599; 10.4995; 17.9405
82.254; 86.522; 88.292		1762Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554788 CIFC41 H48 O2 S2P 1 21/n 111.3446; 17.747; 17.3945
90; 97.039; 90		3475.7Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554789 CIFC13 H18 N2 O2 S2P 1 21/c 110.5966; 11.0075; 13.0168
90; 103.286; 90		1477.67Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554790 CIFC37 H40 O2 S2P 1 21/c 114.4032; 9.233; 24.7181
90; 93.6338; 90		3280.5Hoffmann, Kerstin; Guentner, Manuel; Mayer, Peter; Dube, Henry
Symmetric and nonsymmetric bis-hemithioindigos – precise visible light controlled shape-shifters
Organic Chemistry Frontiers, 2019, 6, 1244
1554791 CIFC21 H15 N3 OP 1 21/c 110.5706; 17.3802; 10.1316
90; 96.996; 90		1847.5Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B
One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides.
Organic letters, 2015, 17, 1184-1187
1554792 CIFC24 H12 F6 SeP 1 21/c 112.234; 10.9831; 14.6454
90; 111.492; 90		1831Shi, Xinzhe; Mao, Shuxin; Roisnel, Thierry; Doucet, Henri; Soulé, Jean-François
Palladium-catalyzed successive C–H bond arylations and annulations toward the π-extension of selenophene-containing aromatic skeletons
Organic Chemistry Frontiers, 2019, 6, 2398
1554793 CIFC24 H21 I N2 O3 SP 21 21 2110.7482; 12.7229; 16.152
90; 90; 90		2208.76Fu, Shaomin; Yang, Honghao; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas.
Organic letters, 2015, 17, 1018-1021
1554794 CIFC19 H24 N2 OP c a 2112.8993; 10.853; 11.6466
90; 90; 90		1630.5Li, Bo; Wang, Si-Qing; Liu, Bin; Shi, Bing-Feng
Synthesis of oxazolines from amides via palladium-catalyzed functionalization of unactivated C(sp(3))-H bond.
Organic letters, 2015, 17, 1200-1203
1554795 CIFC36 H23 Br F3 N2 O3P 21 21 2111.6434; 14.186; 17.6525
90; 90; 90		2915.72Li, Boyu; Gao, Fengyun; Feng, Xing; Sun, Mengmeng; Guo, Yifei; Wen, Dongwa; Deng, Yabo; Huang, Jinqi; Wang, Kairong; Yan, Wenjin
Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole-pyrrolidine]s through organocatalytic cycloaddition
Organic Chemistry Frontiers, 2019, 6, 1567
1554796 CIFC24 H44 B2 N2 O4P b a m12.939; 13.093; 15.573
90; 90; 90		2638.2Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554797 CIFC29 H49 B2 Co N2 O4F d d 218.923; 58.36; 11.127
90; 90; 90		12288Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554798 CIFC24 H46 B2 N2 O5P 1 21/n 110.74; 19.626; 13.066
90; 93.197; 90		2749.8Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto
Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water.
Organic letters, 2015, 17, 1212-1215
1554799 CIFC27 H40 O6P 1 21 19.8327; 16.984; 16.2007
90; 101.138; 90		2654.54Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554800 CIFC29 H44 O6P 21 21 2112.0011; 13.3921; 17.7454
90; 90; 90		2852.04Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554801 CIFC26 H38 O6P 1 21 19.6691; 16.4235; 15.94
90; 101.09; 90		2484.01Zhang, Na; Shi, Zhengyi; Guo, Yi; Xie, Shuangshuang; Qiao, Yuben; Li, Xiao-Nian; Xue, Yongbo; Luo, Zengwei; Zhu, Hucheng; Chen, Chunmei; Hu, Linzhen; Zhang, Yonghui
The absolute configurations of hyperilongenols A–C: rare 12,13-seco-spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
Organic Chemistry Frontiers, 2019, 6, 1491
1554802 CIFC24 H41 B2 O2 PP 1 21/n 18.6014; 17.6656; 16.4517
90; 107.162; 90		2388.51Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554803 CIFC28 H33 B2 Fe O2 PP 1 21 112.674; 9.2986; 12.919
90; 113.497; 90		1396.3Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554804 CIFC40 H43 B2 Fe PP 21 21 2110.3874; 17.4963; 18.3521
90; 90; 90		3335.3Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain
Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes.
Organic letters, 2015, 17, 1216-1219
1554805 CIFC162 H174 Au4 Cl16 O8 P4P -112.983; 13.401; 29.22
81.31; 77.62; 61.97		4376Hau, Franky Ka-Wah; Cheung, Kai-Leung; Zhu, Nianyong; Yam, Vivian Wing-Wah
Calixarene-based alkynyl-bridged gold(i) isocyanide and phosphine complexes as building motifs for the construction of chemosensors and supramolecular architectures
Organic Chemistry Frontiers, 2019, 6, 1205
1554806 CIFC13 H12 O4P 1 21/n 110.5408; 14.0223; 15.567
90; 95.216; 90		2291.4Wang, Hong-Li; Shang, Ming; Sun, Shang-Zheng; Zhou, Zeng-Le; Laforteza, Brian N.; Dai, Hui-Xiong; Yu, Jin-Quan
Cu(II)-catalyzed coupling of aromatic C-H bonds with malonates.
Organic letters, 2015, 17, 1228-1231
1554807 CIFC27 H23 N OP -110.4979; 10.7112; 10.8365
60.7986; 76.2796; 71.3801		1003.08Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy
Organic Chemistry Frontiers, 2019, 6, 1655
1554808 CIFC27 H23 N OP 1 21 16.7344; 18.9552; 15.1244
90; 90.856; 90		1930.4Lustosa, Danilo M.; Cieslik, Patrick; Hartmann, Deborah; Bruckhoff, Tim; Rudolph, Matthias; Rominger, Frank; Hashmi, A. Stephen K.
Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy
Organic Chemistry Frontiers, 2019, 6, 1655
1554809 CIFC19 H18 N O5 S2P -17.9459; 8.3713; 15.0845
98.477; 91.135; 97.754		982.54Deng, Zhimin; Wei, Jialiang; Liao, Lihao; Huang, Haiyan; Zhao, Xiaodan
Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols.
Organic letters, 2015, 17, 1834-1837
1554810 CIFC24 H22 O3C 1 c 114.8194; 23.1341; 17.3079
90; 104.994; 90		5731.7Gelat, Fabien; Richard, Vincent; Berger, Olivier; Montchamp, Jean-Luc
Development of a new family of chiral auxiliaries.
Organic letters, 2015, 17, 1819-1821
1554811 CIFC34 H30 N2 O7P 21 21 219.7212; 10.3208; 28.5171
90; 90; 90		2861.14Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying
A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones
Organic Chemistry Frontiers, 2019, 6, 1485
1554812 CIFC36 H32 F N3 O7P 1 21 111.7466; 12.2636; 22.7319
90; 93.091; 90		3269.89Liu, Xiong-Li; Zuo, Xiong; Wang, Jun-Xin; Chang, Shun-qin; Wei, Qi-Di; Zhou, Ying
A bifunctional pyrazolone–chromone synthon directed organocatalytic double Michael cascade reaction: forging five stereocenters in structurally diverse hexahydroxanthones
Organic Chemistry Frontiers, 2019, 6, 1485
1554813 CIFC17 H16 Cl N3 OP -18.6811; 13.1015; 15.2298
66.74; 82.416; 77.876		1553.57Guo, Xiao; Chen, Wenteng; Chen, Binhui; Huang, Wei; Qi, Weixing; Zhang, Guolin; Yu, Yongping
One-pot three-component strategy for functionalized 2-aminoimidazoles via ring opening of α-nitro epoxides.
Organic letters, 2015, 17, 1157-1159
1554814 CIFC34 H35 N O6 SP 21 21 219.4387; 22.551; 28.131
90; 90; 90		5987.7Peng, Peng; Geng, Yiqun; Göttker-Schnetmann, Inigo; Schmidt, Richard R.
2-Nitro-thioglycosides: α- and β-selective generation and their potential as β-selective glycosyl donors.
Organic letters, 2015, 17, 1421-1424
1554815 CIFC19 H21 F2 N OP 1 21/c 19.9286; 17.0093; 10.0841
90; 90.259; 90		1703He, Zhengbiao; Tan, Ping; Ni, Chuanfa; Hu, Jinbo
Fluoroalkylative aryl migration of conjugated N-arylsulfonylated amides using easily accessible sodium di- and monofluoroalkanesulfinates.
Organic letters, 2015, 17, 1838-1841
1554816 CIFC17 H16 Br F3 O2P 1 21 16.2353; 7.7873; 17.3098
90; 90.759; 90		840.42Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554817 CIFC23 H21 N O7 SP 1 21 110.6202; 6.377; 16.3385
90; 98.252; 90		1095.07Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554818 CIFC18 H17 F3 O3P 21 21 216.4981; 15.2542; 17.146
90; 90; 90		1699.57Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554819 CIFC24 H31 Ag F6 N2 P2P 1 c 115.277; 8.0788; 21.7171
90; 98.481; 90		2651.01Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554820 CIFC31 H41 Ag F6 N4 P2P 1 21/c 112.7111; 17.36; 15.7081
90; 105.588; 90		3338.73Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554821 CIFC25 H31 Ag F3 N2 O PP 1 21/c 111.3702; 12.6386; 17.83
90; 103.361; 90		2492.88Chen, Daoqian; Lu, Long; Shen, Qilong
[Ag(bpy)(PPhtBu2)(OCF3)]: a stable nucleophilic reagent for chemoselective and stereospecific trifluoromethoxylation of secondary alkyl nosylates
Organic Chemistry Frontiers, 2019, 6, 1801
1554822 CIFC16 H10 N2 OP 1 21/n 16.4176; 20.0965; 9.335
90; 98.274; 90		1191.42Chen, Xiaopei; Cui, Xiuling; Yang, Fangfang; Wu, Yangjie
Base-promoted cross-dehydrogenative coupling of quinoline N-oxides with 1,3-azoles.
Organic letters, 2015, 17, 1445-1448
1554823 CIFC27 H40 O4P 21 21 218.061; 10.8588; 27.7356
90; 90; 90		2427.77Xu, Hou-Chao; Hu, Kun; Shi, Xiao-Huo; Tang, Jian-Wei; Li, Xiao-Nian; Sun, Han-Dong; Puno, Pema-Tenzin
Synergistic use of NMR computation and quantitative interproton distance analysis in the structural determination of neokadcoccitane A, a rearranged triterpenoid featuring an aromatic ring D from Kadsura coccinea
Organic Chemistry Frontiers, 2019, 6, 1619
1554824 CIFC20 H14 O5P 1 21/n 19.0391; 9.7069; 17.2285
90; 102.573; 90		1475.41Tian, Yuan; Jiang, Nan; Zhang, Ai Hua; Chen, Chao Jun; Deng, Xin Zhao; Zhang, Wen Jing; Tan, Ren Xiang
Muta-mycosynthesis of naphthalene analogs.
Organic letters, 2015, 17, 1457-1460
1554825 CIFC15 H13 N3P -15.4882; 11.1825; 11.6413
62.292; 80.059; 76.727		613.82Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554826 CIFC17 H17 N3 O2C 1 2/c 115.105; 12.8664; 15.5822
90; 91.952; 90		3026.6Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554827 CIFC19 H17 B F2 N4 O2P -17.1859; 12.0427; 12.0895
93.791; 100.927; 98.538		1011.05Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554828 CIFC17 H16 N3 O2.5P 1 21/c 110.668; 24.498; 11.286
90; 93.034; 90		2945.4Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554829 CIFC17.14 H14.5 B F2 N3 O2P 1 21/c 111.1306; 11.7622; 24.0194
90; 91.217; 90		3143.92Farinone, Marco; Cybińska, Joanna; Pawlicki, Miłosz
A controlled blue-shift in meso-nitrogen aryl fused DIPY and BODIPY skeletons
Organic Chemistry Frontiers, 2019, 6, 2825
1554830 CIFC20 H25 F3 N2 O3 SP 1 21/c 18.128; 15.344; 16.979
90; 102.44; 90		2067.8van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554831 CIFC22 H30 F3 N3 O3 SC 1 2/c 115.441; 10.924; 27.769
90; 90.9; 90		4683.4van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554832 CIFC18 H22 F3 N3 O3 SP 1 21/c 18.4815; 11.074; 21.3223
90; 93.426; 90		1999.1van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554833 CIFC21 H25 N3P -18.61; 9.179; 11.835
93.38; 95.73; 105.2		894.57van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554834 CIFC20 H26 N2P 1 21/c 18.693; 17.464; 11.525
90; 103.69; 90		1700van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554835 CIFC14 H22 N2R 3 c :H26.3163; 26.3163; 10.403
90; 90; 120		6239.3van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop
Base-stabilized nitrilium ions as convenient imine synthons.
Organic letters, 2015, 17, 1461-1464
1554836 CIFC22 H26 N4 O5P 21 21 219.5782; 11.765; 20.2153
90; 90; 90		2278.01Dai, Chuan; Ma, Jun; Li, Min; Wu, Wen; Xia, Xuefeng; Zhang, Jinqiang
Diversity-oriented submonomer synthesis of azapeptides mediated by the Mitsunobu reaction
Organic Chemistry Frontiers, 2019, 6, 2529
1554837 CIFC49 H29 B F20 N O2 RhP 1 21/c 112.2787; 24.2002; 15.5541
90; 101.818; 90		4523.9Otley, Kate D.; Ellman, Jonathan A.
An efficient method for the preparation of styrene derivatives via Rh(III)-catalyzed direct C-H vinylation.
Organic letters, 2015, 17, 1332-1335
1554838 CIFC18 H18 O2P 1 21/c 114.026; 8.7035; 12.0599
90; 104.008; 90		1428.4Liu, Rui; Lu, Ze-Hai; Hu, Xiao-Hui; Li, Jun-Li; Yang, Xian-Jin
Monocarboxylation and intramolecular coupling of butenylated arenes via palladium-catalyzed C-H activation process.
Organic letters, 2015, 17, 1489-1492
1554839 CIFC17 H16 O2 SeP 1 21 16.9078; 10.3981; 10.0732
90; 95.471; 90		720.24Niu, Wenxue; Yeung, Ying-Yeung
Catalytic and highly enantioselective selenolactonization.
Organic letters, 2015, 17, 1660-1663
1554840 CIFC12 H20 O4P 3213.594; 13.594; 5.7493
90; 90; 120		920.11Wang, Hengbin; Negretti, Solymar; Knauff, Allison R.; Montgomery, John
Exo-selective reductive macrocyclization of ynals.
Organic letters, 2015, 17, 1493-1496
1554841 CIFC14 H15 Br N2 O2P 21 21 219.2455; 10.1411; 14.412
90; 90; 90		1351.3Gu, Xiaodong; Dai, Yuanyuan; Guo, Tingting; Franchino, Allegra; Dixon, Darren J.; Ye, Jinxing
A general, scalable, organocatalytic nitro-Michael addition to enones: enantioselective access to all-carbon quaternary stereocenters.
Organic letters, 2015, 17, 1505-1508
1554842 CIFC22 H18 F N3 O2 SP 1 21/c 115.7629; 11.6907; 10.7408
90; 100.958; 90		1943.22Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554843 CIFC16 H23 Cl F6 N3 O2 PC 1 c 110.7226; 12.3939; 15.6108
90; 92.991; 90		2071.77Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554844 CIFC17 H23 Cl2 F6 N2 O2 PP 1 21/c 111.8795; 14.5176; 12.6593
90; 102.138; 90		2134.44Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554845 CIFC28 H41 F6 N4 O2 PC 1 2/c 136.485; 10.158; 16.856
90; 92.44; 90		6241Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554846 CIFC34 H49 F12 N7 O4 P2I 1 2/a 124.915; 8.8562; 19.8464
90; 105.666; 90		4216.5Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554847 CIFC26 H39.5 F9 N4.5 O5 P SP -110.7516; 12.0558; 14.8348
107.62; 93.413; 109.731		1696.8Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554848 CIFC19 H29 Cl F6 N3 O2 PP 1 21/n 17.59057; 26.3895; 12.488
90; 107.133; 90		2390.48Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554849 CIFC21 H32 F6 N4 O2 PP 1 21/c 112.3903; 16.1931; 13.6174
90; 113.783; 90		2500.1Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554850 CIFC16 H23 F12 N3 O2 P2P 1 21/n 110.5891; 16.2883; 13.903
90; 102.985; 90		2336.65Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554851 CIFC26 H41 Cl2 F6 N2 O2 PP 1 21/c 118.6093; 10.778; 15.4265
90; 101.706; 90		3029.76Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554852 CIFC30.33 H52.53 Cl2.12 F6 N3 O2.44 PP -19.5322; 18.6061; 21.1198
83.275; 88.086; 80.993		3673.7Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554853 CIFC22 H35 Cl F6 N3 O2 PP 1 21/n 112.7678; 11.6389; 36.278
90; 94.051; 90		5377.6Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554854 CIFC33 H47.66 F12 N6.5 O4.08 P2P -112.1931; 15.3991; 22.7102
95.65; 102.392; 94.7722		4120.61Devillard, Marc; Regnier, Vianney; Pecaut, Jacques; Martin, David
Stable dicationic dioxoliums and fate of their dioxolyl radicals
Organic Chemistry Frontiers, 2019, 6, 3184
1554855 CIFC18 H21 N3 O2 S2P 1 21/c 110.0095; 11.563; 16.5773
90; 99.859; 90		1890.32Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng
I₂-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles.
Organic letters, 2015, 17, 1521-1524
1554856 CIFC20 H26 N2 O8 SiC 1 2/c 118.687; 6.709; 37.603
90; 90.534; 90		4714Yin, Zhiping; Liu, Zengjin; Huang, Zhenggang; Chu, Yang; Chu, Zhiwen; Hu, Jia; Gao, Lu; Song, Zhenlei
Synthesis of functionalized γ-lactone via Sakurai exo-cyclization/rearrangement of 3,3-bis(silyl) enol ester with a tethered acetal.
Organic letters, 2015, 17, 1553-1556
1554857 CIFC19 H20 O3 SP -16.9512; 8.6039; 15.1128
102.337; 92.466; 108.002		833.95He, Fu-Sheng; Wu, Youqian; Li, Xiaofang; Xia, Hongguang; Wu, Jie
Photoredox-catalyzed sulfonylation of alkenylcyclobutanols with the insertion of sulfur dioxide through semipinacol rearrangement
Organic Chemistry Frontiers, 2019, 6, 1873
1554858 CIFC60 H85 I3 N10 O12P -114.2686; 14.6629; 17.0163
80.443; 70.781; 82.037		3301.6Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554859 CIFC17 H23 N O5 SP 1 21/n 16.0877; 10.8073; 26.052
90; 93.948; 90		1709.9Xu, Dongyang; Wei, Hongbo; Zhen, Yanxia; Gao, Yu-Qi; Li, Ruoxin; Li, Xingzhou; He, Yupeng; Zhang, Zhong; Xie, Weiqing
Carboxylate phosphabetaine as a bifunctional organocatalyst for the intramolecular ring opening of oxetane
Organic Chemistry Frontiers, 2019, 6, 1681
1554860 CIFC60 H78 Cl6 N10 O10C 1 2/c 122.9779; 30.564; 22.926
90; 114.207; 90		14685.1Saha, Subrata; Santra, Saikat; Ghosh, Pradyut
[2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation.
Organic letters, 2015, 17, 1854-1857
1554861 CIFC9 H11 B0.75 O2.25P 1 21/n 16.4968; 22.26; 7.1909
90; 116.2; 90		933.1Bhavanarushi, Sangepu; Xu, Yin; Khan, Imran; Luo, Zhibin; Liu, Bin; Xie, Jimin
Transition-metal-free borylation of propargylic alcohols: structurally variable synthesis in ionic liquid medium
Organic Chemistry Frontiers, 2019, 6, 1895
1554862 CIFC27 H27 F3 N2 O8P -18.5362; 11.0883; 14.8339
89.337; 75.808; 89.011		1360.96Huang, Lin; Zheng, Sheng-Cai; Tan, Bin; Liu, Xin-Yuan
Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes.
Organic letters, 2015, 17, 1589-1592
1554863 CIFC11 H7 F3 N2 O2P 1 21/n 15.41; 17.433; 11.237
90; 93.29; 90		1058Peng, Xiaofeng; Zhang, Xiaofei; Li, Shunyao; Lu, Yunfu; Lan, Lefu; Yang, Chunhao
Silver-mediated synthesis of novel 3-CF3/CN/phosphonate-substituted pyrazoles as pyrrolomycin analogues from 3-formylchromones and diazo compounds
Organic Chemistry Frontiers, 2019, 6, 1775
1554864 CIFC14 H11 N O7P n a 218.6933; 19.9383; 7.6281
90; 90; 90		1322.18Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Substituted quinoline quinones as surrogates for the PQQ cofactor: an electrochemical and computational study.
Organic letters, 2015, 17, 1850-1853
1554865 CIFC24 H22 N2 O9 SP 21 21 2112.2161; 12.5468; 16.7879
90; 90; 90		2573.13Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong
Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes
Organic Chemistry Frontiers, 2019, 6, 1891
1554866 CIFC24 H24 O6P 1 21/c 110.3133; 11.2328; 19.0954
90; 99.604; 90		2181.14Zhou, Qing; Chen, Bo; Huang, Xiao-Bing; Zeng, Ya-Li; Chu, Wen-Dao; He, Long; Liu, Quan-Zhong
Palladium-catalyzed diastereo- and enantioselective formal [3 + 2] cycloaddition of vinyl cyclopropanes with cyclic 1-azadienes
Organic Chemistry Frontiers, 2019, 6, 1891
1554867 CIFC23 H26 Br N O4 SP 1 21 19.8067; 9.9678; 11.8916
90; 104.237; 90		1126.7Serpier, Fabien; Flamme, Benjamin; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain
Chiral pyrrolidines and piperidines from enantioselective rhodium-catalyzed cascade arylative cyclization.
Organic letters, 2015, 17, 1720-1723
1554868 CIFC24 H19 Cl N2 O3P 21 21 215.9309; 17.47; 19.675
90; 90; 90		2038.6Chu, Ming-Ming; Qi, Suo-Suo; Wang, Yi-Feng; Wang, Biao; Jiang, Zhen-Hui; Xu, Dan-Qian; Xu, Zhen-Yuan
Organocatalytic asymmetric [4 + 1] annulation of in situ generated ortho-quinomethanes with 4-halo pyrazolones: straightforward access to chiral spiro-benzofuran pyrazolones
Organic Chemistry Frontiers, 2019, 6, 1977
1554869 CIFC28 H19 N O3 S2P -110.443; 11.228; 11.795
70.186; 87.728; 65.484		1175.6Ming, Wenbo; Liu, Xiaocui; Wang, Lianjie; Liu, Jun; Wang, Mang
Tandem Thien- and benzannulations of α-alkenoyl-α-alkynyl ketene dithioacetals with cyanoacetates: synthesis of functionalized benzo[b]thiophenes.
Organic letters, 2015, 17, 1746-1749
1554870 CIFC19 H18 N2 O4P 1 21/c 19.3579; 12.566; 29.371
90; 96.6; 90		3430.9Zhang, Wei; Zheng, Han-Liang; Liu, Yang; Yu, Ao; Yang, Chen; Li, Xin; Cheng, Jin-Pei
Catalyst-free amination of α-cyanoarylacetates enabled by single-electron transfer
Organic Chemistry Frontiers, 2019, 6, 1900
1554871 CIFC15 H21 N O3P 1 21/n 15.1627; 14.8595; 17.7219
90; 96.198; 90		1351.59Borrero, Nicholas V.; DeRatt, Lindsey G.; Ferreira Barbosa, Lais; Abboud, Khalil A.; Aponick, Aaron
Tandem gold-catalyzed dehydrative cyclization/diels-alder reactions: facile access to indolocarbazole alkaloids.
Organic letters, 2015, 17, 1754-1757
1554872 CIFC28 H29 N3 O4P 1 21 17.807; 15.9924; 10.5193
90; 109.003; 90		1241.79Zhang, Yan-Ping; You, Yong; Zhao, Jian-Qiang; Zhou, Xiao-Jian; Zhang, Xiao-Mei; Xu, Xiao-Ying; Yuan, Wei-Cheng
A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides
Organic Chemistry Frontiers, 2019, 6, 1879
1554873 CIFC20 H16 O2P 21 21 215.9724; 14.8969; 16.4863
90; 90; 90		1466.79Peraino, Nicholas J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Diastereoselective synthesis of γ-lactones through reaction of enediolates with α,β-unsaturated sulfoxonium salts.
Organic letters, 2015, 17, 1735-1737
1554874 CIFC23 H30 O8P 21 21 218.0029; 15.3468; 17.8042
90; 90; 90		2186.69Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554875 CIFC12 H13 Br O2P 1 21/c 16.0066; 11.7969; 16.772
90; 97.594; 90		1178Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554876 CIFC29 H27 N2 O4.5C 1 c 114.3037; 14.0845; 23.7866
90; 91.922; 90		4789.36Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554877 CIFC23 H21 NP 1 21/c 110.4176; 11.9596; 16.0413
90; 114.231; 90		1822.51Che, Chao; Zheng, Hanliang; Zhu, Gangguo
Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides.
Organic letters, 2015, 17, 1617-1620
1554878 CIFC29 H36 N2 O4P 1 21 18.527; 16.7982; 9.3056
90; 102.717; 90		1300.22Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554879 CIFC28.33333 H40.33333 N O9.33333P 21 21 218.09067; 25.4976; 41.3088
90; 90; 90		8521.7Guo, Cui; Wang, Pei; Lin, Xiuping; Salendra, Limbadri; Kong, Fandong; Liao, Shengrong; Yang, Bin; Zhou, Xuefeng; Wang, Junfeng; Liu, Yonghong
Phloroglucinol heterodimers and bis-indolyl alkaloids from the sponge-derived fungus Aspergillus sp. SCSIO 41018
Organic Chemistry Frontiers, 2019, 6, 3053
1554880 CIFC13 H22 O2C 1 c 114.0887; 10.5929; 9.0247
90; 114.771; 90		1222.92Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier
A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates.
Organic letters, 2015, 17, 2054-2057
1554881 CIFC17 H23 N O4P 1 21/c 112.0924; 16.7422; 8.278
90; 107.825; 90		1595.5Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554882 CIFC14 H13 F3 O5P -16.4241; 10.1906; 11.3167
68.951; 83.144; 83.818		684.79Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554883 CIFC17 H20 O4P 1 21/c 112.1636; 10.2486; 12.3402
90; 110.011; 90		1445.5Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554884 CIFC16 H18 O4P 1 21/c 17.6075; 9.2096; 19.424
90; 98.561; 90		1345.7Zhang, Zhen; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
Copper-catalyzed highly diastereoselective cross-dehydrogenative coupling between 8-hydroxyisochromanes and 1,3-dicarbonyl compounds
Organic Chemistry Frontiers, 2019, 6, 2275
1554885 CIFC20 H20 Br2 Cl2 N2 O4P 15.0746; 14.828; 16.699
65.191; 89.579; 80.838		1123.5Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554886 CIFC33 H27 Cl3 N2 O5 SP 21 21 2110.9357; 11.7723; 24.8931
90; 90; 90		3204.7Ren, Xiao-Rui; Lin, Jun-Bing; Hu, Xiu-Qin; Xu, Peng-Fei
Bifunctional Brønsted base catalyzed inverse-electron-demand aza-Diels–Alder reactions of saccharin-derived 1-azadienes with azlactones
Organic Chemistry Frontiers, 2019, 6, 2280
1554887 CIFC13 H15 Br Cl N O3P 1 21 14.8035; 8.2644; 18.363
90; 94.441; 90		726.79Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554888 CIFC10 H9 N O SeP 1 21/c 15.4632; 16.8139; 10.7302
90; 98.574; 90		974.64Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua
Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates
Organic Chemistry Frontiers, 2019, 6, 1967
1554889 CIFC24 H33 N O3 SeP 1 21 110.1323; 7.4394; 15.4852
90; 100.787; 90		1146.62Xiao, Jun-An; Li, Yu-Chun; Cheng, Xiu-Liang; Chen, Wen-Qiang; Cui, Jian-Guo; Huang, Yan-Min; Huang, Jun; Xiao, Qi; Su, Wei; Yang, Hua
Selenocyanobenziodoxolone: a practical electrophilic selenocyanation reagent and its application for solid-state synthesis of α-carbonyl selenocyanates
Organic Chemistry Frontiers, 2019, 6, 1967
1554890 CIFC13 H16 Br Cl2 N O3P 1 21 110.669; 4.7706; 15.964
90; 107.952; 90		773Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554891 CIFC21 H21 Cl O5P 21 21 217.229; 11.212; 22.921
90; 90; 90		1857.8Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554892 CIFC20 H18 O4P 1 21 110.3231; 8.3376; 10.651
90; 116.926; 90		817.35Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554893 CIFC21 H19 Cl O4P 21 21 2110.5134; 7.5193; 22.921
90; 90; 90		1812Lv, Xue-Jiao; Zhao, Wei-Wei; Chen, Ying-Han; Wan, Sheng-Biao; Liu, Yan-Kai
Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways
Organic Chemistry Frontiers, 2019, 6, 1972
1554894 CIFC6 H12 Cl2 O2P 1 21 14.9886; 19.578; 9.0155
90; 92.03; 90		880Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554895 CIFC16 H15 N3 O4 SP 1 21/n 114.05; 8.3338; 14.2852
90; 101.509; 90		1639Wang, Guodong; Sun, Jian; Wang, Kai; Han, Junfen; Li, Hongshuang; Duan, Guiyun; You, Guirong; Li, Furong; Xia, Chengcai
Palladium-catalyzed direct C–H nitration and intramolecular C–H functionalization for the synthesis of 3-nitro-1-(phenylsulfonyl)-1H-indazole derivatives
Organic Chemistry Frontiers, 2019, 6, 1608
1554896 CIFC13 H15 Br Cl N O3P 1 21 112.2792; 4.9357; 13.4763
90; 115.38; 90		737.92Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554897 CIFC16 H19 N O3P 1 21 17.9218; 6.5193; 13.434
90; 101.58; 90		679.67Mandzhulo, Aleksandr; Vashchenko, Iryna; Gerasov, Andrii; Vovk, Mykhaylo; Rusanov, Eduard; Fetyukhin, Volodymyr; Lukin, Oleg; Shivanyuk, Alexander
Selective synthesis of N-protected exo-spiro[oxirane-3,2′-tropanes]
Organic Chemistry Frontiers, 2019, 6, 1692
1554898 CIFC13 H15 Br Cl N O3C 1 2 116.929; 4.841; 36.446
90; 101.211; 90		2930Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554899 CIFC24 H36 O3P 21 21 218.9194; 12.8315; 18.5057
90; 90; 90		2118Zhao, Nan; Xie, Shengling; Tian, Peilin; Tong, Rongbiao; Ning, Chengqing; Xu, Jing
Asymmetric total synthesis of (+)-astellatol and (−)-astellatene
Organic Chemistry Frontiers, 2019, 6, 2014
1554900 CIFC14 H18 Cl N O8 SP 21 21 216.1403; 13.657; 20.719
90; 90; 90		1737.5Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554901 CIFC20 H30 O4P 21 21 219.9964; 10.5385; 17.4587
90; 90; 90		1839.22Zhang, Jing; Tang, Xuli; Han, Xiao; Feng, Danqing; Luo, Xiangchao; Ofwegen, Leen van; Li, Pinglin; Li, Guoqiang
Sarcoglaucins A-I, new antifouling cembrane-type diterpenes from the South China Sea soft coral Sarcophyton glaucum
Organic Chemistry Frontiers, 2019, 6, 2004
1554902 CIFC6 H12 Cl2 O2P 21 21 215.8932; 9.8358; 14.7998
90; 90; 90		857.86Shemet, Andrej; Sarlah, David; Carreira, Erick M.
Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.
Organic letters, 2015, 17, 1878-1881
1554903 CIFC19 H20 N2 O3P 1 21 16.5666; 16.4713; 8.0376
90; 111.405; 90		809.39Wang, Bo; Wang, Yuankai; Wang, Zixuan; Wang, Jianbo
Rh(i)-Catalyzed intramolecular [2 + 2 + 1] cycloaddition of diynes with the N-terminal of the diazo group
Organic Chemistry Frontiers, 2019, 6, 2329
1554904 CIFC18 H14 N2 OP 1 21/c 117.283; 5.72; 16.0086
90; 115.367; 90		1430Bunescu, Ala; Wang, Qian; Zhu, Jieping
Synthesis of functionalized epoxides by copper-catalyzed alkylative epoxidation of allylic alcohols with alkyl nitriles.
Organic letters, 2015, 17, 1890-1893
1554905 CIFC45 H42 F4 O7C 1 2/c 115.1446; 24.455; 20.982
90; 93.45; 90		7756.8Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.
Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight
Organic Chemistry Frontiers, 2019, 6, 1961
1554906 CIFC47 H45 F4 O7P -111.4709; 13.897; 14.895
107.986; 112.427; 96.387		2015.5Wu, Tuoqi; Senior, James; Bremner, Glen; Finden, Jeremy; Branda, Neil R.
Unusual structural changes as a result of weathering benzofuran-based diarylethenes in simulated sunlight
Organic Chemistry Frontiers, 2019, 6, 1961
1554907 CIFC28 H36 N2 O10 Pd3P 1 21/c 18.2684; 13.1049; 14.9823
90; 98.209; 90		1606.8Guo, Kun; Chen, Xiaolan; Guan, Mingyu; Zhao, Yingsheng
Direct ortho-C-H functionalization of aromatic alcohols masked by acetone oxime ether via exo-palladacycle.
Organic letters, 2015, 17, 1802-1805
1554908 CIFC24 H19 N OP 1 21/c 110.273; 10.178; 16.954
90; 99.61; 90		1747.8Zhao, Hong-Ping; Ma, Xiao-Pan; Nie, Shu-Min; Xiao, Yuhong; Mo, Dong-Liang
Synthesis of chromeno[4,3-b]quinolines and spirobenzofuran-3,3′-quinolines through silver-mediated Appel reaction/C–Br bond cleavage/double selective rearrangement sequence
Organic Chemistry Frontiers, 2019, 6, 2334
1554909 CIFC21 H24 B N O2P 1 21/n 19.82013; 15.1033; 12.9881
90; 93.8267; 90		1922.05Pareek, Manish; Fallon, Thomas; Oestreich, Martin
Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 2082-2085
1554910 CIFC30 H21 N O2P 1 21/n 110.5982; 10.2369; 20.9415
90; 99.629; 90		2240Wang, Jian; Cai, Panyuan; He, Yimiao; Liu, Yuan; Zhong, Ling; Ding, Shumin; Shang, Yongjia
Tuneable access to isoquinolines via a transition-metal-free C(sp3)–C(sp3) bond cleavage rearrangement reaction
Organic Chemistry Frontiers, 2019, 6, 2430
1554911 CIFC27 H29 F6 N2 O P RuP -110.7138; 10.8978; 12.099
92.748; 96.702; 90.476		1401.24Hong, Xi; Zhou, Quan; Huang, Shuang; Cui, He-Zhen; Li, Zhi-Ming; Hou, Xiu-Feng
Transition metal catalysed C7 and ortho-selective halogenation of 2-arylbenzo[d]oxazoles
Organic Chemistry Frontiers, 2019, 6, 2226
1554912 CIFC20 H41 B2 F8 N5 OP 21 21 219.9728; 10.8425; 25.575
90; 90; 90		2765.4Mirabdolbaghi, Roya; Dudding, Travis
Expanding the forefront of strong organic Brønsted acids: proton-catalyzed hydroamination of unactivated alkenes and activation of Au(I) for alkyne hydroamination.
Organic letters, 2015, 17, 1930-1933
1554913 CIFC14 H12 N2 OP 21 21 216.8959; 7.1261; 24.02
90; 90; 90		1180.4Feng, Guang-Shou; Zhao, Zi-Biao; Shi, Lei; Zhou, Yong-Gui
Iridium-catalyzed asymmetric hydrogenation of quinazolinones
Organic Chemistry Frontiers, 2019, 6, 2250
1554914 CIFC25 H36 F3 N3 O4P -17.9555; 12.7291; 14.1773
101.894; 105.578; 101.34		1304Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554915 CIFC20 H27 F3 N2 O3P 1 21/c 19.676; 6.0187; 35.338
90; 90.313; 90		2057.9Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554916 CIFC18 H23 F3 N2 O3P -18.4082; 8.9935; 12.6932
109.241; 90.111; 102.16		883.25Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554917 CIFC18 H16 F3 N OP 21 21 215.8836; 19.2027; 26.5181
90; 90; 90		2996Geoghegan, Kimberly; Bode, Jeffrey W.
Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles.
Organic letters, 2015, 17, 1934-1937
1554918 CIFC35 H27 Br F3 N3 O3P 21 21 218.4795; 18.0358; 21.5437
90; 90; 90		3294.78Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing
Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
Organic Chemistry Frontiers, 2019, 6, 1989
1554919 CIFC40 H31 Cl2 F4 N2 O3P 21 21 2111.9726; 16.0021; 18.2529
90; 90; 90		3497.01Zhao, Xiaoyun; Xiong, Jiale; An, Junkai; Yu, Jicong; Zhu, Liping; Feng, Xing; Jiang, Xianxing
Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocenters via asymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
Organic Chemistry Frontiers, 2019, 6, 1989
1554920 CIFC21 H16 N2 O2 SC 1 c 113.529; 16.7566; 8.6938
90; 116.175; 90		1768.8Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
1554921 CIFC24 H24 N2 O2 SP 1 21/c 112.5268; 10.8502; 16.3904
90; 103.482; 90		2166.4Lee, Dong Jin; Yoo, Eun Jeong
Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions.
Organic letters, 2015, 17, 1830-1833
1554922 CIFC31 H28 N2 O5P n a 2121.4324; 13.5256; 8.8733
90; 90; 90		2572.2Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei
Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes
Organic Chemistry Frontiers, 2019, 6, 2415
1554923 CIFC30 H25 N3 O3P -18.9859; 10.004; 15.8029
97.57; 90.211; 115.564		1267.4Zhang, Si-Chen; Lei, Xin-Xin; Yang, Yong-jian; Luo, Yong-Chun; Zhang, Huan-Huan; Xu, Peng-Fei
Palladium catalysed [3 + 2]-annulation reaction of vinylcyclopropanes with pentafulvenes: synthesis of polysubstituted spiro[4,4]nona-6,8-dienes
Organic Chemistry Frontiers, 2019, 6, 2415
1554924 CIFC19 H29 F N2 O5 SiP 21 21 216.42; 8.0707; 40.1927
90; 90; 90		2082.54Istrate, Alena; Medvecky, Michal; Leumann, Christian J.
2'-Fluorination of tricyclo-DNA controls furanose conformation and increases RNA affinity.
Organic letters, 2015, 17, 1950-1953
1554925 CIFC38 H31 Br Cl3 N3 O4P 21 21 219.1965; 9.694; 38.3086
90; 90; 90		3415.2Zhang, Jing; Chan, Wai-Lun; Chen, Ligong; Ullah, Nisar; Lu, Yixin
Creation of bispiro[pyrazolone-3,3′-oxindoles] via a phosphine-catalyzed enantioselective [3 + 2] annulation of the Morita–Baylis–Hillman carbonates with pyrazoloneyldiene oxindoles
Organic Chemistry Frontiers, 2019, 6, 2210
1554926 CIFC19 H16 N2 O4P 1 21 17.5248; 11.7969; 18.7512
90; 98.035; 90		1648.2Bisai, Vishnumaya; Unhale, Rajshekhar A.; Suneja, Arun; Dhanasekaran, Sivasankaran; Singh, Vinod K.
An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence.
Organic letters, 2015, 17, 2102-2105
1554927 CIFC16 H18 OR 3 :H20.961; 20.961; 7.086
90; 90; 120		2696.2Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554928 CIFC27 H34 O3 SiC 1 2/c 142.742; 10.4771; 10.9037
90; 93.609; 90		4873.1Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554929 CIFC14 H18 O5P -17.3423; 8.4321; 10.4623
85.681; 85.985; 78.332		631.55Lin, Minggui; Cui, Hao; Hua, Yuhui; Zhang, Yandong
Domino enyne metathesis en route to skeletally diverse, privileged scaffolds: synthesis of the tricyclic core of pseudolaric acid F
Organic Chemistry Frontiers, 2019, 6, 2771
1554930 CIFC16 H25 N O2 S3P 21 21 215.36225; 12.0412; 27.5363
90; 90; 90		1777.96Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554931 CIFC18 H19 N O4 SP b c a17.4772; 10.488; 19.6463
90; 90; 90		3601.2Huang, Guofei; Ren, Xiaoyu; Jiang, Chunhui; Wu, Jia-Hong; Gao, Guowei; Wang, Tianli
Efficient synthesis of (E)-2-nitromethylcinnamates via phosphine-catalyzed tandem α-addition and 1,3-rearrangement
Organic Chemistry Frontiers, 2019, 6, 2872
1554932 CIFC18 H19 Cl F3 N O SP 1 21 111.7646; 15.4251; 12.0356
90; 118.452; 90		1920.3Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554933 CIFC10 H8 N2 SP n a 2115.971; 4.2214; 13.319
90; 90; 90		898Peng, Yingyuan; He, Qian; Zhang, Xiaofei; Yang, Chunhao
Pd-Catalyzed intramolecular C–H activation and C–S formation to synthesize pyrazolo[5,1-b]benzothiazoles without an additional oxidant
Organic Chemistry Frontiers, 2019, 6, 3234
1554934 CIFC19 H23 Fe N O2 SP 1 21 15.84461; 11.3132; 13.829
90; 95.4227; 90		910.298Das, Manas; O'Shea, Donal F
Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines.
Organic letters, 2015, 17, 1962-1965
1554935 CIFC23 H17 Cl O2P 1 21/m 19.353; 7.448; 12.251
90; 93.725; 90		851.6Liu, Yang; Jin, Shiyu; Huang, Liping; Hu, Youhong
Phase transfer reagent promoted tandem ring-opening and ring-closing reactions of unique 3-(1-alkynyl) chromones.
Organic letters, 2015, 17, 2134-2137
1554936 CIFC20 H21 N3 O4P 1 21/n 110.8238; 10.3557; 17.8199
90; 96.908; 90		1982.9Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554937 CIFC133 H116 N8 O21 S4P 1 21 110.8299; 17.8426; 16.7462
90; 105.418; 90		3119.5Xie, Danbo; Yang, Limin; Lin, Youqiang; Zhang, Zhiming; Chen, Dongdong; Zeng, Xiaofei; Zhong, Guofu
Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals.
Organic letters, 2015, 17, 2318-2321
1554938 CIFC20 H21 N3 O4P 42 b c21.7832; 21.7832; 8.49552
90; 90; 90		4031.19Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554939 CIFC15 H13 N3 O2P -16.9944; 7.8586; 26.1858
85.696; 89.837; 79.658		1411.87Zhang, Xiang; Huang, Qing-Fei; Zou, Wen-Lin; Li, Qing-Zhu; Feng, Xin; Jia, Zhi-Qiang; Liu, Yue; Li, Jun-Long; Wang, Qi-Wei
Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates
Organic Chemistry Frontiers, 2019, 6, 3321
1554940 CIFC22 H18 F3 N O3P 21 21 219.69927; 10.835; 16.94975
90; 90; 90		1781.28Rabasa-Alcañiz, Fernando; Hammerl, Daniel; Sánchez-Merino, Anabel; Tejero, Tomás; Merino, Pedro; Fustero, Santos; del Pozo, Carlos
Asymmetric synthesis of polycyclic 3-fluoroalkylproline derivatives by intramolecular azomethine ylide cycloaddition
Organic Chemistry Frontiers, 2019, 6, 2916
1554941 CIFC39 H30 Cl N OP 1 21/n 114.7817; 10.4931; 20.1054
90; 110.04; 90		2929.66Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554942 CIFC26 H20 Cu F6 PP b c n15.5529; 7.3629; 19.8862
90; 90; 90		2277.26Liu, He; Shen, Qilong
Bistrifluoromethylated organocuprate [Ph4P]+[Cu(CF3)2]−: synthesis, characterization and its application for trifluoromethylation of activated heteroaryl bromides, chlorides and iodides
Organic Chemistry Frontiers, 2019, 6, 2324
1554943 CIFC20 H22 N2 O4P 1 21/c 110.5905; 16.0282; 11.3851
90; 116.637; 90		1727.47Yakkala, Prasanna Anjaneyulu; Giri, Deepesh; Chaudhary, Bharatkumar; Auti, Prashant; Sharma, Satyasheel
Regioselective C–H alkylation and alkenylation at the C5 position of 2-amino-1,4-naphthoquinones with maleimides under Rh(iii) catalysis
Organic Chemistry Frontiers, 2019, 6, 2441
1554944 CIFC24 H24 Cl N OP 1 21/n 112.0241; 10.8634; 15.0306
90; 92.829; 90		1960.94Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554945 CIFC17 H15 Br2 N O2P -17.5896; 10.9767; 11.9609
110.338; 100.049; 106.048		856.49Wang, Yu-Chao; Wang, Rui-Xiang; Qiu, Guanyinsheng; Zhou, Hongwei; Xie, Wenlin; Liu, Jin-Biao
ortho-Amide-directed 2,4-dibromohydration of conjugated enynes
Organic Chemistry Frontiers, 2019, 6, 2471
1554946 CIFC14 H12 N2 OP -17.2536; 9.2341; 9.3515
85.065; 81.059; 68.355		574.85Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines
Organic Chemistry Frontiers, 2019, 6, 2404
1554947 CIFC25 H15 N3 OP 1 21/n 19.8811; 14.4238; 13.7948
90; 109.258; 90		1856.1Su, Han; Bao, Ming; Pei, Chao; Hu, Wenhao; Qiu, Lihua; Xu, Xinfang
Gold-catalyzed dual annulation of azide-tethered alkynes with nitriles: expeditious synthesis of oxazolo[4,5-c]quinolines
Organic Chemistry Frontiers, 2019, 6, 2404
1554948 CIFC24 H24 Cl N OP 1 21/c 116.3879; 7.0026; 17.8667
90; 103.718; 90		1991.86Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H.
Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization.
Organic letters, 2015, 17, 1986-1989
1554949 CIFC25 H23 F2 N O3 SP -18.0332; 8.5272; 16.9075
99.329; 99.436; 101.204		1097.99Hu, Xiao-Si; Ding, Pei-Gang; Yu, Jin-Sheng; Zhou, Jian
A Sc(OTf)3 catalyzed Mukaiyama–Mannich reaction of difluoroenoxysilanes with unactivated ketimines
Organic Chemistry Frontiers, 2019, 6, 2500
1554950 CIFC152.5 H199 B4 N7 O23P 1 21/c 111.705; 28.512; 22.406
90; 98.94; 90		7387Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554951 CIFC24 H24 O2 S2C 1 2 123.8323; 5.5909; 15.658
90; 103.617; 90		2027.7Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554952 CIFC25 H25 N O2 SP 21 21 216.07714; 13.1618; 27.1117
90; 90; 90		2168.56Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554953 CIFC32 H30.52 O4.26 SC 1 2/c 113.9336; 19.7182; 20.3209
90; 103.298; 90		5433.4Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554954 CIFC27 H24 Fe O2 SP b c a28.3482; 19.5347; 7.5873
90; 90; 90		4201.6Shoji, Taku; Miura, Kota; Ohta, Akira; Sekiguchi, Ryuta; Ito, Shunji; Endo, Yuya; Nagahata, Tatsuki; Mori, Shigeki; Okujima, Tetsuo
Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties
Organic Chemistry Frontiers, 2019, 6, 2801
1554955 CIFC50 H44 F24 N4 P4P 1 21/n 113.488; 14.281; 14.287
90; 108.36; 90		2611.9Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554956 CIFC186 H168 B4 N14 O31P -116.134; 16.609; 16.766
85.82; 65.15; 75.26		3939.7Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554957 CIFC27 H22 Cl N O5 SP 21 21 2110.1603; 10.173; 23.5179
90; 90; 90		2430.83Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun
Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes
Organic Chemistry Frontiers, 2019, 6, 2452
1554958 CIFC27 H23 N O5 SP 1 21 110.0757; 10.4448; 10.8094
90; 92.786; 90		1136.2Lin, Wei; Lin, Xiao; Cheng, Yuyu; Chang, Xiaoyong; Zhou, San; Li, Pengfei; Li, Wenjun
Organocatalytic enantioselective direct vinylogous Michael addition of γ-substituted deconjugate butenolides to azadienes
Organic Chemistry Frontiers, 2019, 6, 2452
1554959 CIFC117 H171 B4 N4 O20P 1 21/c 142.193; 8.356; 15.63
90; 90.76; 90		5510.1Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554960 CIFC180 H112 B4 D84 N4 O34 S14P -116.67; 17.44; 19.659
81.21; 74.06; 62.19		4859Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Nestable Tetrakis(spiroborate) Nanocycles.
Organic letters, 2015, 17, 2154-2157
1554961 CIFC30 H29 N O3 SP 1 21/n 19.8296; 13.4413; 22.608
90; 94.433; 90		2978.1Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554962 CIFC20 H27 N O2 SP 21 21 215.8832; 8.7875; 37.5443
90; 90; 90		1940.99Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554963 CIFC22 H29 N O2 SP 21 21 218.87; 10.6671; 21.508
90; 90; 90		2035Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554964 CIFC19 H23 N O2 SC 1 2/c 135.164; 8.6573; 11.5114
90; 94.241; 90		3494.8Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554965 CIFC23 H33 N O2 SP 1 21/c 119.505; 8.6857; 13.1687
90; 92.309; 90		2229.2Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554966 CIFC21 H26 Br N O2 SP 1 21 110.888; 8.651; 10.91
90; 97.5; 90		1018.8Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554967 CIFC18 H22 Br N O2 SP 1 21/c 112.551; 11.012; 14.276
90; 113.904; 90		1803.9Rui, Kang-Hua; Yang, Song; Wei, Yin; Shi, Min
Rh(i)-Catalyzed stereoselective intramolecular cycloaddition reactions of ene-vinylidenecyclopropanes for the construction of fused 6,5-bicyclic skeletons with a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2019, 6, 2506
1554968 CIFC70 H56 N8 O8P -111.446; 13.451; 22.036
98.71; 104.3; 98.36		3189.9Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554969 CIFC32 H26 N4 O2C 1 2/c 116.098; 8.0852; 19.417
90; 103.12; 90		2461.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554970 CIFC17 H14 ClP -110.013; 12.073; 12.827
111.893; 107.027; 93.776		1348.7Fan, Xing; Liu, Ruixing; Wei, Yin; Shi, Min
Rh-Catalyzed intramolecular decarbonylative cyclization of ortho-formyl group tethered alkylidenecyclopropanes (ACPs) for the construction of 2-methylindenes
Organic Chemistry Frontiers, 2019, 6, 2667
1554971 CIFC34 H30 N4 O4P 1 21/c 17.3964; 23.302; 16.073
90; 94.05; 90		2763.3Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554972 CIFC20 H17 N OP b c a14.5964; 13.9382; 14.6669
90; 90; 90		2983.94Hu, Xiaoping; Wang, Gaonan; Qin, Chunxiang; Xie, Xin; Zhang, Chunli; Xu, Wei; Liu, Yuanhong
Ligandless nickel-catalyzed transfer hydrogenation of alkenes and alkynes using water as the hydrogen donor
Organic Chemistry Frontiers, 2019, 6, 2619
1554973 CIFC70 H58 Cl6 N8 O12 SC 1 c 137.78; 8.9173; 26.953
90; 133.41; 90		6596Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David
Quaterpyrroles as building blocks for the synthesis of expanded porphyrins.
Organic letters, 2015, 17, 2194-2197
1554974 CIFC30 H27 N3P 1 21/n 114.929; 5.74297; 27.7627
90; 104.785; 90		2301.48Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554975 CIFC17 H16 N2P 1 21/c 115.534; 6.291; 15.0837
90; 113.849; 90		1348.18Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554976 CIFC15 H13 N3P c a 2112.9687; 13.0705; 7.18
90; 90; 90		1217.06Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554977 CIFC22 H17 N3P -18.8058; 10.1568; 10.8636
112.118; 90.659; 106.96		852.87Zhu, Yingzu; Li, Yinghua; Xiang, Shiqun; Fan, Weibin; Jin, Jiang; Huang, Deguang
Utilization of nitriles as the nitrogen source: practical and economical construction of 4-aminopyrimidine and β-enaminonitrile skeletons
Organic Chemistry Frontiers, 2019, 6, 3071
1554978 CIFC16 H10 Br N O4P 1 21/c 112.4447; 15.6502; 7.9646
90; 105.739; 90		1493Bag, Raghunath; Sar, Dinabandhu; Punniyamurthy, Tharmalingam
Copper(II)-catalyzed direct dioxygenation of alkenes with air and N-hydroxyphthalimide: synthesis of β-keto-N-alkoxyphthalimides.
Organic letters, 2015, 17, 2010-2013
1554979 CIFC30 H24 F2 O5P 1 21/n 114.1655; 22.469; 16.419
90; 98.419; 90		5169.6Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin
Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling
Organic Chemistry Frontiers, 2019, 6, 2788
1554980 CIFC15 H12 F O3P -19.9135; 11.2232; 13.3885
94.007; 107.02; 109.916		1315.15Liu, Baohua; Mao, Chunyan; Hu, Qiong; Yao, Liangliang; Hu, Yimin
Direct methylation and carbonylation of in situ generated arynes via HDDA-Wittig coupling
Organic Chemistry Frontiers, 2019, 6, 2788
1554981 CIFC70 H120 N14 O26 S8P -113.0106; 13.1402; 14.3888
80.344; 63.999; 78.993		2160.42Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554982 CIFC30 H60 N12 O16 S4C 1 2/c 113.4741; 14.6965; 22.6791
90; 92.704; 90		4485.96Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554983 CIFC19 H19 B11 Cl6 OP 1 21/c 117.251; 12.1706; 26.112
90; 91.879; 90		5479.4Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554984 CIFC20 H21 B11 Cl6 OP b c a19.0146; 13.8372; 21.2518
90; 90; 90		5591.5Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554985 CIFC25 H22 B11 Cl6 NP b c n18.70332; 18.4574; 18.4002
90; 90; 90		6352.02Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554986 CIFC25 H22 B11 Cl6 NP b c n18.015; 14.8013; 23.3476
90; 90; 90		6225.53Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554987 CIFC25 H24 B11 Cl6 NP 1 21/c 131.445; 13.6072; 32.634
90; 116.666; 90		12478.2Lu, Mengsi; Allemann, Oliver; Xu, Jun; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S.
Peraryl-X-onium ions of nitrogen and oxygen
Organic Chemistry Frontiers, 2019, 6, 2640
1554988 CIFC40 H69.97 N4 O14 S4P -111.2634; 15.966; 16.009
111.587; 100.691; 109.004		2373.6Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
New "pyrene box" cages for adaptive guest conformations.
Organic letters, 2015, 17, 2178-2181
1554989 CIFC27 H24 N4 O4 S2P 1 21/n 19.943; 19.423; 27.408
90; 94.84; 90		5274.24Wang, Lihong; Wang, Xiaomin; Zhang, Ge; Yang, Shengbiao; Li, Yan; Zhang, Qian
Copper-catalyzed 1,3-aminoazidation of arylcyclopropanes: a facile access to 1,3-diamine derivatives
Organic Chemistry Frontiers, 2019, 6, 2934
1554990 CIFC15 H13 N O4 SP 21 21 218.1609; 9.0398; 19.318
90; 90; 90		1425.1Liu, Yan-Kai; Li, Zhi-Long; Li, Ji-Yao; Feng, Huan-Xi; Tong, Zhi-Ping
Open-close: an alternative strategy to α-functionalization of lactone via enamine catalysis in one pot under mild conditions.
Organic letters, 2015, 17, 2022-2025
1554991 CIFC13 H11 N O3P 1 21/c 19.4606; 8.7844; 13.698
90; 91.45; 90		1138Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion
Organic Chemistry Frontiers, 2019, 6, 2420
1554992 CIFC15 H13 N O3P 21 21 215.2776; 10.8907; 22.1326
90; 90; 90		1272.11Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion
Organic Chemistry Frontiers, 2019, 6, 2420
1554993 CIFC14 H11 N O5P 1 21/c 111.0859; 9.2256; 12.6525
90; 101.245; 90		1269.2Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure: kinetic resolution and further conversion
Organic Chemistry Frontiers, 2019, 6, 2420
1554994 CIFC28 H23 N3 O4 SP 1 21/n 112.8623; 11.3355; 16.9579
90; 94.493; 90		2464.87Chen, Jing; Li, Jianjun; Wang, Jiazhe; Li, Hao; Wang, Wei; Guo, Yuewei
Phosphine-Catalyzed Aza-MBH Reactions of Vinylpyridines: Efficient and Rapid Access to 2,3,5-Triarylsubstituted 3-Pyrrolines.
Organic letters, 2015, 17, 2214-2217
1554995 CIFC23 H18 Cl N O2P -19.2832; 10.0044; 11.107
87.027; 65.546; 82.335		930.61Yao, Yongqi; Yang, Wen; Lin, Qifu; Yang, Weitao; Li, Huanyong; Wang, Lin; Gu, Fenglong; Yang, Dingqiao
1,3-Dipolar cycloaddition of nitrones to oxa(aza)bicyclic alkenes
Organic Chemistry Frontiers, 2019, 6, 3360
1554996 CIFC19 H22 O7P 1 21/n 16.0808; 23.3393; 12.5225
90; 94.028; 90		1772.82Tan, Ceheng; Chen, Wei; Mu, Xinpeng; Chen, Qi; Gong, Jianxian; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2338-2341
1554997 CIFC21 H18 N4 O4 SP 21 21 216.0211; 16.1241; 20.634
90; 90; 90		2003.25Li, Shi-Wu; Du, Yu; Kang, Qiang
A chiral-at-metal asymmetric catalyzed vinylogous Michael addition of ortho-methyl aromatic nitro compounds for isoxazole derivative synthesis
Organic Chemistry Frontiers, 2019, 6, 2775
1554998 CIFC26 H31 Br N2 O3P -19.6121; 11.761; 13.648
98.331; 109.571; 113.637		1260.2Zeng, Xiao-Hua; Wang, Hong-Mei; Ding, Ming-Wu
Unexpected Synthesis of 5,6-Dihydropyridin-2(1H)-ones by a Domino Ugi/Aldol/Hydrolysis Reaction Starting from Baylis-Hillman Phosphonium Salts.
Organic letters, 2015, 17, 2234-2237
1554999 CIFC40 H32 O6P -110.438; 10.7; 15.172
80.197; 70.129; 79.638		1556.7Wang, Wenli; Tang, Yingzhan; Liu, Yongxiang; Yuan, Lei; Wang, Jian; Lin, Bin; Zhou, Di; Sun, Lu; Huang, Renbin; Chen, Gang; Li, Ning
Isolation, structure elucidation, and synthesis of (±)-millpuline A with a suppressive effect in miR-144 expression
Organic Chemistry Frontiers, 2019, 6, 2850
1555000 CIFC38 H44 B2 F4 N4 O6P -19.7881; 13.2333; 16.5195
67.596; 77.669; 72.069		1870.86Huaulmé, Quentin; Mirloup, Antoine; Retailleau, Pascal; Ziessel, Raymond
Synthesis of Highly Functionalized BOPHY Chromophores Displaying Large Stokes Shifts.
Organic letters, 2015, 17, 2246-2249
1555001 CIFC44 H40 N4 Ni O2P 1 21/c 119.861; 13.383; 18.29
90; 117.363; 90		4318Ren, Demin; Fu, Xinliang; Li, Xiaofang; Koniarz, Sebastian; Chmielewski, Piotr J.
Reaction of antiaromatic porphyrinoid with active methylene compounds
Organic Chemistry Frontiers, 2019, 6, 2924
1555002 CIFC15 H16 N2 O4P 1 21/c 114.1112; 4.6513; 21.124
90; 99.827; 90		1366.14Mei, Xiangui; Lan, Mengmeng; Cui, Guodong; Zhang, Hongwei; Zhu, Weiming
Caerulomycins from Actinoalloteichus cyanogriseus WH1-2216-6: isolation, identification and cytotoxicity
Organic Chemistry Frontiers, 2019, 6, 3566
1555003 CIFC27 H30 F N O2P -19.3088; 9.5092; 14.5742
92.724; 104.673; 110		1159.92Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555004 CIFC28 H32 F N O2P 21 21 218.03153; 10.686; 28.3689
90; 90; 90		2434.76Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555005 CIFC28 H32 N4 O2P 32 2 111.32263; 11.32263; 35.383
90; 90; 120		3928.44Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555006 CIFC30 H35 N O4P 19.7073; 10.168; 14.0374
85.597; 85.998; 82.306		1366.53Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555007 CIFC28 H31 F2 N O2P 110.4764; 10.6867; 12.3768
85.757; 70.552; 69.477		1222.26Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555008 CIFC28 H31 F2 N O2P 1 21 17.90952; 16.3522; 9.53794
90; 95.6737; 90		1227.58Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E.
Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines.
Organic letters, 2015, 17, 2254-2257
1555009 CIFC24 H20 O SP 1 21/n 115.8263; 7.7607; 15.9189
90; 106.393; 90		1875.73Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua
Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones
Organic Chemistry Frontiers, 2019, 6, 2796
1555010 CIFC22 H14 Cl F O SP -17.3464; 8.5371; 15.0907
95.337; 91.518; 104.361		911.69Liu, Changqing; Wang, Bo; Guo, Ziyi; Zhang, Jitan; Xie, Meihua
Metal-free cascade rearrangement/radical addition/oxidative C–H annulation of propargyl alcohols with sodium sulfinates: access to 2-sulfenylindenones
Organic Chemistry Frontiers, 2019, 6, 2796
1555011 CIFC23 H27 Br N2 O5P 1 21/n 18.3956; 11.6027; 23.715
90; 91.1454; 90		2309.7Arai, Takayoshi; Tsuchiya, Kento; Matsumura, Eri
PyBidine-NiCl2-Catalyzed Asymmetric Addition of Alcohols and Peroxides to Isatin-Derived Ketimines.
Organic letters, 2015, 17, 2416-2419
1555012 CIFC8 H11 F3 N2 O SP 1 21/c 18.4044; 11.3774; 11.5451
90; 96.16; 90		1097.6Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng
Copper-Catalyzed Intermolecular Trifluoromethylthiocyanation of Alkenes: Convenient Access to CF3-Containing Alkyl Thiocyanates.
Organic letters, 2015, 17, 2438-2441
1555013 CIFC147 H132 N16 O27 ZnP 1 21/a 123.94; 28.05; 23.991
90; 119.85; 90		13973Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555014 CIFC38 H32 N2 O6P 1 21/n 112.6219; 16.3765; 16.6547
90; 100.607; 90		3383.7Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555015 CIFC15 H16 O3P 1 21/n 14.6619; 23.4349; 12.2946
90; 97.466; 90		1331.8Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555016 CIFC152 H128 N8 O24 ZnP -112.8844; 13.9073; 20.6328
98.862; 106.525; 94.899		3469.4Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555017 CIFC36 H30 N4 O6P 1 21/n 112.8709; 15.6947; 16.5272
90; 92.507; 90		3335.38Husain, Ali; Ganesan, Asaithampi; Ghazal, Basma; Durmuş, Mahmut; Zhang, Xian-Fu; Makhseed, Saad
Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms
Organic Chemistry Frontiers, 2019, 6, 3192
1555018 CIFC76 H112 F14 N4 Sn4P -110.7975; 11.121; 17.986
82.945; 76.059; 70.925		1978.74Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555019 CIFC32 H4 F26 N4P -16.15317; 9.3804; 13.8177
103.878; 100.265; 98.23		747.31Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H.
Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives.
Organic letters, 2015, 17, 2266-2269
1555020 CIFC26 H18 OC 1 2/c 142.263; 7.4986; 12.0012
90; 93.813; 90		3794.9Han, Jian; Liu, Xinbang; Li, Yu; Lou, Zihao; Yi, Mingdong; Kong, Huihui; Luo, Jun
New synthetic approaches for hexacene and its application in thin-film transistors
Organic Chemistry Frontiers, 2019, 6, 2839
1555021 CIFC19 H18 O2P n a 2112.91; 9.664; 12.157
90; 90; 90		1516.7Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.
Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.
Organic letters, 2015, 17, 2278-2281
1555022 CIFC17 H22 O2P 21 21 218.6511; 11.009; 15.784
90; 90; 90		1503.3Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J.
Michael Additions of Highly Basic Enolates to ortho-Quinone Methides.
Organic letters, 2015, 17, 2278-2281
1555023 CIFC24 H17 N O2P -111.0804; 12.2799; 13.6018
75.764; 84.604; 89.194		1785.88Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie
One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes
Organic Chemistry Frontiers, 2019, 6, 2897
1555024 CIFC24 H17 N O2P 1 21/c 18.5534; 5.4976; 37.5979
90; 93.982; 90		1763.7Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie
One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes
Organic Chemistry Frontiers, 2019, 6, 2897
1555025 CIFC26 H18 F3 N O2P -16.4787; 10.7989; 16.2052
79.201; 85.566; 73.057		1065.03Yang, Zhijia; Pi, Chao; Cui, Xiuling; Wu, Yangjie
One-pot synthesis of pyranoquinolin-1-ones via Rh(iii)-catalysed redox annulation of 3-carboxyquinolines and alkynes
Organic Chemistry Frontiers, 2019, 6, 2897
1555026 CIFC22 H21 N O3P -19.724; 10.178; 10.676
62.165; 79.328; 69.089		872.6Capreti, Naylil M. R.; Jurberg, Igor D.
Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds.
Organic letters, 2015, 17, 2490-2493
1555027 CIFC28 H22 O3 SP 1 21/c 110.465; 9.797; 22.032
90; 95.834; 90		2247.1Yang, Tao; Kou, Peihao; Jin, Fengyan; Song, Xian-Rong; Bai, Jiang; Ding, Haixin; Xiao, Qiang; Liang, Yong-Min
TFA-promoted sulfonation/cascade cyclization of 2-propynolphenols with sodium sulfinates to 4-sulfonyl 2H-chromenes under metal-free conditions
Organic Chemistry Frontiers, 2019, 6, 3162
1555028 CIFC15 H13 N OR -3 :H26.4383; 26.4383; 8.6956
90; 90; 120		5263.8Zhang, Yan; Wang, Dahai; Cui, Sunliang
Facile Synthesis of Isoindolinones via Rh(III)-Catalyzed One-Pot Reaction of Benzamides, Ketones, and Hydrazines.
Organic letters, 2015, 17, 2494-2497
1555029 CIFC17 H15 N O3 SP 1 21/n 15.9669; 11.4767; 21.9463
90; 96.78; 90		1492.38Zhu, Cheng-Zhi; Wei, Yin; Shi, Min
Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives
Organic Chemistry Frontiers, 2019, 6, 2884
1555030 CIFC21 H16 Br N O4 SP -17.1629; 10.9804; 12.5285
102.431; 97.658; 98.768		936.85Zhu, Cheng-Zhi; Wei, Yin; Shi, Min
Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives
Organic Chemistry Frontiers, 2019, 6, 2884
1555031 CIFC36 H39 N O2P 1 21/c 114.8225; 11.0736; 18.657
90; 100.056; 90		3015.3Reddy, Virsinha; Vijaya Anand, Ramasamy
Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach.
Organic letters, 2015, 17, 3390-3393
1555032 CIFC27 H20 N2 O4 SP -19.0601; 9.927; 13.5869
82.759; 78.19; 83.39		1181.56Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides
Organic Chemistry Frontiers, 2019, 6, 2968
1555033 CIFC29.25 H25.5 Cl0.5 N3 O6 S2P 1 21/c 112.7222; 31.291; 7.7018
90; 104.211; 90		2972.2Zhang, Tian-Shu; Wang, Rong; Cai, Pei-Jun; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides
Organic Chemistry Frontiers, 2019, 6, 2968
1555034 CIFC25 H27 Fe N O3 SP 1 21 115.0789; 8.6357; 18.2167
90; 106.122; 90		2278.8Ogasawara, Masamichi; Wada, Shiro; Isshiki, Erika; Kamimura, Takumi; Yanagisawa, Akira; Takahashi, Tamotsu; Yoshida, Kazuhiro
Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library.
Organic letters, 2015, 17, 2286-2289
1555035 CIFC88 H73 Cl10 N3 PdC 1 2/c 117.9223; 20.5932; 21.0729
90; 100.834; 90		7638.9Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou
Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination
Organic Chemistry Frontiers, 2019, 6, 3292
1555036 CIFC84 H65 Cl2 N3 O2 PdC 1 2/c 117.6466; 20.7167; 20.3473
90; 95.896; 90		7399.2Zhang, Fei-Yi; Lan, Xiao-Bing; Xu, Chang; Yao, Hua-Gang; Li, Tian; Liu, Feng-Shou
Rigid hindered N-heterocyclic carbene palladium precatalysts: synthesis, characterization and catalytic amination
Organic Chemistry Frontiers, 2019, 6, 3292
1555037 CIFC17 H14 N2 O3P 1 21/c 18.9224; 9.3813; 18.2533
90; 103.064; 90		1488.32Son, Jeong-Yu; Kim, Sunghwa; Jeon, Woo Hyung; Lee, Phil Ho
Synthesis of Cinnolin-3(2H)-one Derivatives from Rh-Catalyzed Reaction of Azobenzenes with Diazotized Meldrum's Acid.
Organic letters, 2015, 17, 2518-2521
1555038 CIFC9 H13 N5 O4P 1 21/c 18.3117; 17.2043; 8.3018
90; 103.231; 90		1155.62Guo, Xiaowei; Wang, Jidong; Su, Can; Liu, Chongxi; Ma, Xiao-Yan; Yu, Zhiyin; Li, Jiansong; Wang, Xiangjing; Xiang, Wensheng; Huang, Sheng-Xiong
A unique spiro-β-triazinedione-γ-hydantoin type alkaloid with antiviral activity against tobacco mosaic virus from Streptomyces gamaensis
Organic Chemistry Frontiers, 2019, 6, 3215
1555039 CIFC26 H28 O5P -110.896; 11.118; 11.442
109.812; 100.766; 111.223		1137.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555040 CIFC23 H25 N O9 SP -19.3448; 11.2047; 12.9889
106.439; 97.223; 112.631		1160.92Xing, Siyang; Xia, Hanyu; Wang, Xin; Wu, Die; Xu, Xinrui; Su, Yunran; Wang, Kui; Zhu, Bolin; Guo, Junshuo
Diastereoselective access to 2-aminoindanones via the rhodium(ii)-catalyzed tandem reaction involving O–H insertion and Michael addition
Organic Chemistry Frontiers, 2019, 6, 3121
1555041 CIFC23 H24 O3P -18.428; 11.011; 11.459
65.415; 87.993; 89.668		966.4Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula
Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products.
Organic letters, 2015, 17, 3446-3449
1555042 CIFC33 H38 N O5P 19.1302; 9.1578; 10.226
108.986; 98.417; 114.037		698.83Freeman, Jared L.; Brimble, Margaret A.; Furkert, Daniel P.
A chiral auxiliary-based synthesis of the C5‒C17 trans-decalin framework of anthracimycin
Organic Chemistry Frontiers, 2019, 6, 2954
1555043 CIFC25 H28 O10I 1 2 111.9189; 6.5987; 26.7335
90; 100.124; 90		2069.83Pan, Dongyan; Zhang, Xuexia; Zheng, Haizhou; Zheng, Zhihui; Nong, Xuhua; Liang, Xiao; Ma, Xuan; Qi, Shuhua
Novel anthraquinone derivatives as inhibitors of protein tyrosine phosphatases and indoleamine 2,3-dioxygenase 1 from the deep-sea derived fungus Alternaria tenuissima DFFSCS013
Organic Chemistry Frontiers, 2019, 6, 3252
1555044 CIFC21 H36 O4 SiC 1 2 122.265; 7.7011; 12.8529
90; 102.095; 90		2154.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555045 CIFC12 H14 O3P 1 21/c 112.324; 7.8713; 10.6532
90; 92.217; 90		1032.65Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555046 CIFC23 H20 O6P -17.7957; 10.1827; 12.7574
79.033; 76.634; 77.369		950.96Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555047 CIFC16 H11 Br O2P 1 21/c 110.0036; 15.567; 8.7599
90; 100.953; 90		1339.3Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555048 CIFC16 H12 O2C 1 2/c 125.676; 4.1792; 24.335
90; 112.38; 90		2414.6Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555049 CIFC23 H22 O6P 1 21/c 114.7414; 8.7416; 16.409
90; 104.242; 90		2049.53Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555050 CIFC22 H17 Cl O6P 1 21/n 114.6483; 17.4042; 15.2455
90; 94.817; 90		3872.99Li, Qingrui; Yin, Yunnian; Li, Yabo; Zhang, Jianye; Huang, Mengmeng; Kim, Jung Keun; Wu, Yangjie
A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate
Organic Chemistry Frontiers, 2019, 6, 3238
1555051 CIFC36 H55 N O7 Si2P -18.9128; 10.9914; 20.184
91.339; 96.624; 104.357		1899.99Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555052 CIFC15 H20 O5P 21 21 217.3936; 10.5735; 17.817
90; 90; 90		1392.9Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555053 CIFC21 H38 O5 SP 1 21/c 116.4753; 10.1532; 13.8282
90; 98.669; 90		2286.71Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555054 CIFC21 H22 O10P 1 21/c 18.8935; 14.433; 15.7451
90; 92.016; 90		2019.79Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A‒E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555055 CIFC20 H20 O10P -19.016; 9.3778; 10.636
93.717; 90.826; 92.317		896.52Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555056 CIFC21 H22 O11P c a 218.33914; 13.29606; 18.06836
90; 90; 90		2003.38Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555057 CIFC21 H22 O11P 21 21 218.2302; 14.4554; 16.2394
90; 90; 90		1932.01Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555058 CIFC22 H23 N O9P 1 21/n 18.26703; 13.79202; 17.73644
90; 102.392; 90		1975.18Zang, Yi; Gong, Yi-Hua; Li, Xu-Wen; Li, Xiao-Nian; Liu, Jun-Jun; Chen, Chun-Mei; Zhou, Yuan; Gu, Liang-Hu; Luo, Zeng-Wei; Wang, Jian-Ping; Sun, Wei-Guang; Zhu, Hu-Cheng; Zhang, Yong-Hui
Canescones A–E: aromatic polyketide dimers with PTP1B inhibitory activity from Penicillium canescens
Organic Chemistry Frontiers, 2019, 6, 3274
1555059 CIFC15 H22 O6P 1 21/n 18.5281; 18.7862; 9.5185
90; 100.368; 90		1500.07Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555060 CIFC16 H17 N O4P 1 21 16.9082; 11.2913; 19.3834
90; 91.357; 90		1511.53Peng, Shao-Zheng; Sha, Chin-Kang
Stereoselective Total Syntheses of Guanacastepenes N and O.
Organic letters, 2015, 17, 3486-3489
1555061 CIFC34 H22 Cl2 N4 O4P b c a10.6177; 21.038; 26.249
90; 90; 90		5863.4Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555062 CIFC23 H19 F3P 1 21/c 110.7304; 18.6098; 9.9301
90; 115.595; 90		1788.36Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555063 CIFC24 H21 F3 O2P -19.28774; 13.98378; 16.25245
94.589; 106.279; 98.2135		1989.34Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555064 CIFC24 H20 F4 O2P 1 21/n 18.7646; 10.6788; 20.8962
90; 94.821; 90		1948.87Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555065 CIFC24 H21 F3P -19.7671; 10.3099; 19.8876
92.41; 96.248; 107.45		1893.23Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555066 CIFC24 H21 F3 O2P -18.8501; 10.1181; 11.7209
98.214; 105.322; 103.258		961.85Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555067 CIFC23 H19 F3 OP -19.9918; 10.2089; 10.5751
91.174; 116.274; 107.926		904.65Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555068 CIFC24 H21 F3P -18.9463; 10.2875; 11.0964
70.184; 86.437; 76.947		935.84Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555069 CIFC24 H20 Cl F3 O2P -19.0216; 9.9831; 11.9107
77.527; 82.086; 74.544		1005.86Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555070 CIFC25 H23 F3P 1 21/c 110.5544; 15.4584; 12.2743
90; 102.702; 90		1953.59Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555071 CIFC24 H21 F3P 1 21/n 111.6641; 9.1396; 17.3076
90; 95.883; 90		1835.36Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555072 CIFC22 H16 Br F3P -19.02917; 9.25385; 11.1048
87.5911; 80.5904; 78.3143		896.36Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555073 CIFC24 H19 Cl2 F3 O2P -19.2224; 10.2968; 11.9735
74.791; 80.463; 72.449		1041.48Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555074 CIFC22 H15 Cl2 F3I 1 2/c 121.8668; 10.36934; 18.0539
90; 113.947; 90		3741.25Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555075 CIFC24 H21 F3P 1 21/c 110.1714; 36.8462; 10.1929
90; 103.732; 90		3710.88Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555076 CIFC25 H23 F3 O2P 1 21/c 111.5733; 18.729; 19.4741
90; 105.635; 90		4064.94Zerov, Aleksey V.; Bulova, Anastasia A.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.
TfOH-promoted transformation of TMS-ethers of diarylsubstituted CF3-allyl alcohols with arenes into CF3-indanes
Organic Chemistry Frontiers, 2019, 6, 3264
1555077 CIFC30 H22 Cl2 N4 O12P 4310.6627; 10.6627; 29.5381
90; 90; 90		3358.3Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555078 CIFC29 H20 I4 O4P -112.1779; 21.8512; 21.9539
60.52; 87.603; 86.921		5077.5Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555079 CIFC16 H13 N O3P 1 c 114.099; 5.2916; 9.1495
90; 101.496; 90		668.92He, Guangke; Li, Yuan; Yu, Zilun; Chen, Zhaoqiang; Tang, Yongming; Song, Guangliang; Loh, Teck-Peng
Selectfluor™-catalyzed oxidative cyclization of ynamides enables facile synthesis of oxazolidine-2,4-diones
Organic Chemistry Frontiers, 2019, 6, 3644
1555080 CIFC38 H26 Cl2 O4P 1 21/c 113.2235; 24.195; 10.2868
90; 110.556; 90		3081.6Pop, Lidia; Dumitru, Florina; Hădade, Niculina D; Legrand, Yves-Marie; van der Lee, Arie; Barboiu, Mihail; Grosu, Ion
Exclusive Hydrophobic Self-Assembly of Adaptive Solid-State Networks of Octasubstituted 9,9'-Spirobifluorenes.
Organic letters, 2015, 17, 3494-3497
1555081 CIFC17 H12 I N3 SP 1 21/n 14.12; 14.2279; 26.763
90; 94.268; 90		1564.5Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling
Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals
Organic Chemistry Frontiers, 2019, 6, 3355
1555082 CIFC19 H17 N O S2P b c a10.1327; 12.0719; 28.967
90; 90; 90		3543.3Zhou, Yao; Lou, Yixian; Wang, Ya; Song, Qiuling
Oxidant-controlled divergent transformations of 3-aminoindazoles for the synthesis of pyrimido[1,2-b]-indazoles and aromatic nitrile-derived dithioacetals
Organic Chemistry Frontiers, 2019, 6, 3355
1555083 CIFC19 H21 N O4 SP 1 21/n 18.2569; 11.0688; 20.1396
90; 95.9683; 90		1830.66Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555084 CIFC26 H16 F9 N O4P 1 21/c 16.1329; 40.065; 10.6098
90; 103.811; 90		2531.6He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng
Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers
Organic Chemistry Frontiers, 2019, 6, 3575
1555085 CIFC19 H12 Cl F9 OP c a 2111.543; 10.4; 32.618
90; 90; 90		3916He, Wei; Yu, Jipan; Wang, Dawei; Ran, Guoxia; Xia, Xiao-Feng
Synthesis of tri-substituted allyl alcohols via a copper/iron co-catalyzed cascade perfluoroalkylation/rearrangement of aryl propynyl ethers
Organic Chemistry Frontiers, 2019, 6, 3575
1555086 CIFC27 H27 N O5 SP 1 21/n 110.98; 21.409; 11.347
90; 104.07; 90		2587.3Jung, Da Jung; Jeon, Hyun Ji; Lee, Joo Hyun; Lee, Sang-gi
Cu(I)/Rh(II)-Catalyzed Tandem Convergent Multicomponent Reaction for the Regio- and Stereocontrolled Synthesis of γ-Oxo-β-amino Esters.
Organic letters, 2015, 17, 3498-3501
1555087 CIFC10 H9 F3 N2 OP 21 21 217.1385; 7.5039; 19.126
90; 90; 90		1024.5Wang, Xiaonan; Gao, Yuan; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng
An enantioselective aza-Henry reaction of trifluoromethyl ketimines catalyzed by phase-transfer catalysts
Organic Chemistry Frontiers, 2019, 6, 3269
1555088 CIFC26 H20 Cl F3 N2 O2C 1 c 17.2179; 17.509; 18.867
90; 100.172; 90		2346.9Yu, Yang; Zhang, Yan; Wang, Zhuo; Liang, Yong-Xin; Zhao, Yu-Long
A rhodium-catalyzed three-component reaction of arylisocyanides, trifluorodiazoethane, and activated methylene isocyanides or azomethine ylides: an efficient synthesis of trifluoroethyl-substituted imidazoles
Organic Chemistry Frontiers, 2019, 6, 3657
1555089 CIFC38 H34 P2P -18.6263; 12.097; 16.023
107.86; 95.73; 104.279		1514.1Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555090 CIFC32 H32 O P2P 1 21/c 114.7596; 10.4392; 17.7877
90; 105.924; 90		2635.5Hu, Zhengsong; Li, Zongyang; Zhao, Kang; Tian, Rongqiang; Duan, Zheng; Mathey, François
Reaction of Phospholes with Aldimines: A One-Step Synthesis of Chelating, Alpha-C2-Bridged Biphospholes.
Organic letters, 2015, 17, 3518-3520
1555091 CIFC18 H23 N O2P 1 21/c 112.58; 15.83; 8.839
90; 109.551; 90		1658.7Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555092 CIFC46 H40 O8P 1 21/n 110.1647; 17.2468; 20.8692
90; 101.136; 90		3589.7Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan
Constructing bridged multifunctional calixarenes by intramolecular indole coupling
Organic Chemistry Frontiers, 2019, 6, 3327
1555093 CIFC72 H64 N10 O6P 1 21/c 116.5782; 28.2895; 17.3002
90; 93.414; 90		8099.2Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan
Constructing bridged multifunctional calixarenes by intramolecular indole coupling
Organic Chemistry Frontiers, 2019, 6, 3327
1555094 CIFC76 H68 N8 O8C 1 2/c 130.104; 23.487; 26.09
90; 121.557; 90		15719Bolshchikov, Boris; Volkov, Sergey; Sokolova, Daria; Gorbunov, Alexander; Serebryannikova, Alina; Gloriozov, Igor; Cheshkov, Dmitry; Bezzubov, Stanislav; Chung, Wen-Sheng; Kovalev, Vladimir; Vatsouro, Ivan
Constructing bridged multifunctional calixarenes by intramolecular indole coupling
Organic Chemistry Frontiers, 2019, 6, 3327
1555095 CIFC19 H16 O2C 1 2 117.095; 5.874; 15.476
90; 106; 90		1493.8Ren, Wenlong; Chang, Wenju; Wang, Yang; Li, Jingfu; Shi, Yian
Pd-Catalyzed Regiodivergent Hydroesterification of Aryl Olefins with Phenyl Formate.
Organic letters, 2015, 17, 3544-3547
1555096 CIFC21 H13 Cl I3 N O2P -18.885; 11.599; 11.638
87.07; 72.279; 76.183		1109.11Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555097 CIFC18 H14 Cl N3P 1 21/n 114.445; 6.6377; 15.6545
90; 94.414; 90		1496.53Surendra Reddy, G.; Ramachary, Dhevalapally B.
Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2019, 6, 3620
1555098 CIFC23 H16 N4C 1 c 113.055; 13.601; 10.697
90; 100.788; 90		1865.8Surendra Reddy, G.; Ramachary, Dhevalapally B.
Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2019, 6, 3620
1555099 CIFC23 H14 F N3 O2P -19.293; 13.946; 16.068
114.567; 99.86; 93.392		1846.1Surendra Reddy, G.; Ramachary, Dhevalapally B.
Reaction engineering and photophysical studies of fully enriched C-vinyl-1,2,3-triazoles
Organic Chemistry Frontiers, 2019, 6, 3620
1555100 CIFC21 H15 Cl I N O2P 1 21/n 111.057; 13.631; 13.716
90; 110.38; 90		1937.8Zhang, Xue; Feng, Chengjie; Jiang, Tao; Li, Yifei; Pan, Ling; Xu, Xianxiu
Expedient and Divergent Tandem One-Pot Synthesis of Benz[e]indole and Spiro[indene-1,3'-pyrrole] Derivatives from Alkyne-Tethered Chalcones/Cinnamates and TosMIC.
Organic letters, 2015, 17, 3576-3579
1555101 CIFC25 H22 F N O5P 21 21 218.9187; 14.6101; 16.5218
90; 90; 90		2152.8Bhattacharya, Aditya; mani Shukla, Pushpendra; Kumar Kaushik, Lalit; Maji, Biswajit
Synthesis of chromans and kinetic resolution of 2-aryl-3-nitro-2H-chromenes via the NHC-bound azolium homoenolate pathway
Organic Chemistry Frontiers, 2019, 6, 3523
1555102 CIFC22 H22 OP -19.1622; 9.508; 10.568
83; 65.519; 78.417		820Manojveer, Seetharaman; Balamurugan, Rengarajan
In Situ Formed Acetal-Facilitated Synthesis of Substituted Indene Derivatives from o-Alkenylbenzaldehydes.
Organic letters, 2015, 17, 3600-3603
1555103 CIFC22 H21 N O3 SC 1 2/c 119.5977; 8.1238; 23.2996
90; 90.182; 90		3709.5Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan
Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles
Organic Chemistry Frontiers, 2019, 6, 3415
1555104 CIFC23 H22 Br3 Cl2 N O3 SP -18.199; 11.3055; 14.2419
100.441; 100.282; 91.136		1275.6Chen, Xiaoyan; Zhou, Hao; Chen, Zhiyuan
Pd/P/dba-Promoted cascade annulations to produce fused medium-sized sulfoximine polyheterocycles
Organic Chemistry Frontiers, 2019, 6, 3415
1555105 CIFC8 H10 O4P c a 2110.571; 5.838; 12.338
90; 90; 90		761.4Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555106 CIFC12 H14 O6F d d 237.2102; 18.06; 6.8155
90; 90; 90		4580.1Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555107 CIFC10 H12 O3P b c a8.8394; 8.5924; 23.437
90; 90; 90		1780.1Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555108 CIFC9 H12 O4P 21 21 216.345; 8.9881; 15.108
90; 90; 90		861.6Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555109 CIFC8 H10 O4P 1 21 15.3883; 12.812; 6.0438
90; 114.32; 90		380.21Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan
Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks.
Organic letters, 2015, 17, 3604-3607
1555110 CIFC26 H20 O3 SP 21 21 217.9759; 16.1628; 31.7213
90; 90; 90		4089.3Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan
A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds
Organic Chemistry Frontiers, 2019, 6, 3259
1555111 CIFC27 H21 N O3 SP 21 21 215.7472; 16.912; 22.0104
90; 90; 90		2139.34Dočekal, Vojtěch; Formánek, Bedřich; Císařová, Ivana; Veselý, Jan
A formal [4 + 2] cycloaddition of sulfur-containing alkylidene heterocycles with allenic compounds
Organic Chemistry Frontiers, 2019, 6, 3259
1555112 CIFC19 H22 N2 OP 21 21 217.4987; 12.2482; 16.8063
90; 90; 90		1543.58Wong, Suet-Pick; Gan, Chew-Yan; Lim, Kuan-Hon; Ting, Kang-Nee; Low, Yun-Yee; Kam, Toh-Seok
Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor.
Organic letters, 2015, 17, 3628-3631
1555113 CIFC33 H25 Cl N2 O5P 110.596; 11.6796; 12.6988
69.855; 70.549; 88.791		1383.42Wang, Zhen-Hua; Lei, Chuan-Wen; Zhang, Xia-Yan; You, Yong; Zhao, Jian-Qiang; Yuan, Wei-Cheng
Asymmetric domino 1,6-addition/annulation reaction of 3-cyano-4-alkenyl-2H-chromen-2-ones with isatin-derived MBH carbonates: enantioselective synthesis of 3,3′-cyclopentenylspirooxindoles bearing 2H-chromen-2-ones
Organic Chemistry Frontiers, 2019, 6, 3342
1555114 CIFC18 H23 N O5 SP 18.6291; 9.4332; 12.4474
82.659; 70.506; 68.236		887.04Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555115 CIFC33 H29 Cl N2 O3P 1 21/n 117.7343; 13.4538; 24.68
90; 94.67; 90		5868.9Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555116 CIFC44 H39 N3 O7P -19.853; 14.0452; 15.201
111.663; 93.543; 102.84		1882Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555117 CIFC33 H29 N3 O5P 1 21/n 112.847; 12.739; 20.208
90; 96.73; 90		3284.4Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555118 CIFC34 H28 Cl2 N2 O3P b c a10.1992; 17.1094; 33.448
90; 90; 90		5836.7Wu, Wen-Tao; Han, Ying; Sun, Jing; Yan, Chao-Guo
Efficient construction of pyrrolo[1′,2′:1,2]azocino[4,5-c]quinolines via cascade cycloaddition and annulation reaction
Organic Chemistry Frontiers, 2019, 6, 3530
1555119 CIFC12 H15 F N2 O4 SP 1 21/n 16.70613; 8.92562; 21.9646
90; 91.7362; 90		1314.12Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555120 CIFC20 H40 N3 O5 PP -19.2786; 9.5213; 15.4265
75.673; 76.438; 71.3		1232.75Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide
Enzymatic triggering of C–ON bond homolysis of alkoxyamines
Organic Chemistry Frontiers, 2019, 6, 3663
1555121 CIFC20 H38 N3 O4 PP 1 21/c 18.8282; 22.0666; 12.5309
90; 96.936; 90		2423.3Audran, Gérard; Bosco, Lionel; Brémond, Paul; Jugniot, Natacha; Marque, Sylvain R. A.; Massot, Philippe; Mellet, Philippe; Moussounda Moussounda Koumba, Tataye; Parzy, Elodie; Rivot, Angélique; Thiaudière, Eric; Voisin, Pierre; Wedl, Carina; Yamasaki, Toshihide
Enzymatic triggering of C–ON bond homolysis of alkoxyamines
Organic Chemistry Frontiers, 2019, 6, 3663
1555122 CIFC11 H14 N2 O2 SP 1 21/n 115.2033; 5.10542; 15.6074
90; 108.006; 90		1152.1Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555123 CIFC25 H24 OP 1 21/c 110.22; 9.55; 20.071
90; 93.737; 90		1954.8Li, Hexin; Zhang, Mengru; Mehfooz, Haroon; Zhu, Dongxia; Zhao, Jinbo; Zhang, Qian
Highly convergent modular access to poly-carbon substituted cyclopropanes via Cu(i)-catalyzed three-component cyclopropene carboallylation
Organic Chemistry Frontiers, 2019, 6, 3387
1555124 CIFC16 H16 N2 O2 SP 1 21/n 18.236; 21.1919; 8.4904
90; 103.856; 90		1438.76Hsueh, Nathanael; Clarkson, Guy J.; Shipman, Michael
Generation and Ring Opening of Aziridines in Telescoped Continuous Flow Processes.
Organic letters, 2015, 17, 3632-3635
1555125 CIFC22 H18 Br Cl3 N2 O4P 1 21 113.3229; 6.2024; 15.4655
90; 115.145; 90		1156.87Zhao, Mei-Xin; Liu, Qiang; Yu, Kun-Ming; Zhao, Xiao-Li; Shi, Min
Organocatalyzed asymmetric formal [3 + 2] cycloaddition of isocyanoacetates with N-itaconimides: facile access to optically active spiropyrroline succinimide derivatives
Organic Chemistry Frontiers, 2019, 6, 3879
1555126 CIFC13 H19 N O3 SP 21 21 217.789; 11.669; 15.029
90; 90; 90		1366Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555127 CIFC13 H10 F3 N OP -15.0942; 9.6532; 11.935
91.045; 91.275; 101.201		575.43Lu, Kui; Wei, Xianfu; Li, Quan; Li, Yuxuan; Ji, Liangshuo; Hua, Erbing; Dai, Yujie; Zhao, Xia
Synthesis of α-trifluoromethyl ethanone oximes via the three-component reaction of aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent
Organic Chemistry Frontiers, 2019, 6, 3766
1555128 CIFC14 H17 Br Cl N O4 SP 1 21 19.24; 6.262; 14.504
90; 91.561; 90		838.9Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555129 CIFC15 H30 O4P 17.0302; 7.6119; 7.7844
94.191; 109.731; 97.56		385.61Song, Yin-Ping; Miao, Feng-Ping; Yin, Xiu-Li; Ji, Nai-Yun
Nitrogenous cyclonerane sesquiterpenes from an algicolous strain of Trichoderma asperellum
Organic Chemistry Frontiers, 2019, 6, 3698
1555130 CIFC20 H24 Br N O4 SP 1 21 114.656; 10.051; 14.998
90; 104.87; 90		2135.3Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555131 CIFC16 H9 N3 O2 SP 21 21 215.168; 15.6589; 15.9344
90; 90; 90		1289.49Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina
Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution
Organic Chemistry Frontiers, 2019, 6, 3300
1555132 CIFC16 H10 Br N3 O2 SP -18.3252; 9.8395; 11.1869
65.08; 71.705; 67.231		753.73Recio, Javier; Pérez-Redondo, Adrián; Alvarez-Builla, Julio; Burgos, Carolina
Access to 2-substituted 1-pyridin-3-yl-β-carboline derivatives by intramolecular radical cyclization-ring opening-SNAr substitution
Organic Chemistry Frontiers, 2019, 6, 3300
1555133 CIFC14 H18 Br N O4 SP 1 21 16.4495; 15.276; 8.0516
90; 96.47; 90		788.2Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555134 CIFC20 H23 Br Cl N O4 SP 21 21 217.6751; 12.59; 22.275
90; 90; 90		2152.4Liu, Weigang; Pan, Hongjie; Tian, Hua; Shi, Yian
Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex.
Organic letters, 2015, 17, 3956-3959
1555135 CIFC40 H41 N O4 S2P -111.0456; 12.0988; 14.8761
68.867; 70.725; 86.448		1746.7Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui
A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
Organic letters, 2015, 17, 4128-4131
1555136 CIFC27 H25 N O3 SP -17.8518; 10.3592; 14.2099
80.043; 83.223; 82.438		1123.12Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555137 CIFC26 H22 Cl N O3 SP 1 21/c 15.9034; 21.165; 21.6677
90; 91.308; 90		2706.6Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555138 CIFC24 H18 Cl N O3 SP -19.3704; 10.2251; 11.2595
76.2532; 78.5679; 75.2513		1002.43Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555139 CIFC23 H17 N O4 SP 1 21/c 17.8538; 13.4956; 17.2047
90; 101.145; 90		1789.2Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555140 CIFC23 H16 N2 O5 SP 1 21/c 113.0035; 15.8463; 9.5395
90; 101.719; 90		1924.7Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555141 CIFC24 H21 N O3 SP 21 21 217.3838; 11.2551; 24.298
90; 90; 90		2019.3Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555142 CIFC24 H21 N O3 S2P 1 21/n 19.2819; 23.5334; 10.2751
90; 111.152; 90		2093.2Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555143 CIFC20 H15 N O5 SP -18.2024; 10.5566; 11.0975
68.8504; 79.7504; 71.2427		846.51Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555144 CIFC37 H30 N2 O3 S2P 1 2/n 111.095; 12.561; 24.147
90; 93.088; 90		3360.3Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555145 CIFC31 H26 N2 O4 S2P 1 21/n 18.9049; 14.0612; 22.343
90; 93.263; 90		2793.1Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555146 CIFC35 H22 Cl2 N2 O3 S2C 1 2/c 118.289; 13.2118; 24.2095
90; 91.165; 90		5848.5Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555147 CIFC32 H28 N2 O4 S2P -17.6623; 10.2269; 19.008
102.84; 91.559; 103.009		1410.29Sun, Jing; Sun, Quan-Shun; Yan, Chao-Guo
Efficient synthesis of novel cyclic fused-phenothiazines via domino cyclization of 2-(benzo[b][1,4]thiazin-3-ylidene)acetate, aromatic aldehydes and cyclic 1,3-diketones
Organic Chemistry Frontiers, 2019, 6, 3555
1555148 CIFC43 H48 N O3 S2P 21 21 2111.13642; 14.74032; 46.2616
90; 90; 90		7594.04Ding, Ran; Zheng, Bo; Wang, Yan; Peng, Yungui
A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
Organic letters, 2015, 17, 4128-4131
1555149 CIFC8 H8 N2 O4P 21 21 214.888; 9.8; 18.388
90; 90; 90		880.8Salahifar, Eslam; Nematollahi, Davood; Bayat, Mehdi; Mahyari, Amir; Amiri Rudbari, Hadi
Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives.
Organic letters, 2015, 17, 4666-4669
1555150 CIFC25 H34.5 F3 N O1.25C 1 2 120.6626; 10.3356; 13.6724
90; 123.325; 90		2439.76Sampaio-Dias, Ivo E.; Silva-Reis, Sara C.; Pinto da Silva, Luís; García-Mera, Xerardo; Maestro, Miguel A.; Rodríguez-Borges, José E.
Mechanistic insights for the transprotection of tertiary amines with Boc2O via charged carbamates: access to both enantiomers of 2-azanorbornane-3-exo-carboxylic acids
Organic Chemistry Frontiers, 2019, 6, 3540
1555151 CIFC21 H23 N OP 1 21/c 19.1308; 14.0389; 14.7904
90; 106.943; 90		1813.6Sinai, Ádám; Vangel, Dóra; Gáti, Tamás; Bombicz, Petra; Novák, Zoltán
Utilization of Copper-Catalyzed Carboarylation-Ring Closure for the Synthesis of New Oxazoline Derivatives.
Organic letters, 2015, 17, 4136-4139
1555152 CIFC20 H21 N O3 SC 1 2/c 133.942; 11.5163; 9.4629
90; 99.03; 90		3653.1Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni
Diastereoselective bicyclization of enynols via gold catalysis
Organic Chemistry Frontiers, 2019, 6, 3584
1555153 CIFC17 H16 O2P 21 21 217.3872; 10.8747; 16.4977
90; 90; 90		1325.32Cecchini, Chiara; Cera, Gianpiero; Lanzi, Matteo; Marchiò, Luciano; Malacria, Max; Maestri, Giovanni
Diastereoselective bicyclization of enynols via gold catalysis
Organic Chemistry Frontiers, 2019, 6, 3584
1555154 CIFC14 H11 Cl N2P 1 21/n 115.4081; 7.7461; 19.9246
90; 98.208; 90		2353.69Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555155 CIFC19 H14 Cl N2 O PP 1 21/c 111.949; 8.5662; 17.479
90; 103.621; 90		1738.8Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555156 CIFC30 H38 O7P 1 21/c 111.8298; 17.6502; 13.5929
90; 90.058; 90		2838.17Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan
A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines
Organic Chemistry Frontiers, 2019, 6, 3535
1555157 CIFC31 H38 N2 O6P 1 21/c 111.2677; 10.9396; 24.121
90; 93.117; 90		2968.86Feng, Ziwen; Yuan, Zhenbo; Zhao, Xiaobin; Huang, Yue; Yao, Hequan
A [4 + 1] annulation of ortho-electrophile-substituted para-quinone methides for the synthesis of indanes and isoindolines
Organic Chemistry Frontiers, 2019, 6, 3535
1555158 CIFC7 H3 Cl2 N2P b c a11.4945; 7.5152; 17.4299
90; 90; 90		1505.66Xiao, Xinsheng; Xie, Ying; Bai, Siyi; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei
Transition-Metal-Free Tandem Chlorocyclization of Amines with Carboxylic Acids: Access to Chloroimidazo[1,2-α]pyridines.
Organic letters, 2015, 17, 3998-4001
1555159 CIFC20 H19 N O5P 1 21 110.0737; 6.1334; 13.8766
90; 107.776; 90		816.45Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong
Clavipines A–C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes
Organic Chemistry Frontiers, 2019, 6, 3759
1555160 CIFC16 H14 O5P 21 21 218.594; 11.8962; 13.1105
90; 90; 90		1340.36Sun, Zhaocui; Zhu, Nailiang; Zhou, Man; Huo, Xiaowei; Wu, Haifeng; Tian, Yu; Yang, Junshan; Ma, Guoxu; Yang, Yan-Long; Xu, Xudong
Clavipines A‒C, antiproliferative meroterpenoids with a fused azepine skeleton from the basidiomycete Clitocybe clavipes
Organic Chemistry Frontiers, 2019, 6, 3759
1555161 CIFC23 H24 O4P 1 21/c 18.759; 21.523; 10.067
90; 104.55; 90		1837Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555162 CIFC18 H20 O6P 1 21/c 17.7505; 21.813; 9.5132
90; 94.65; 90		1603Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555163 CIFC16.5 H16 Cl1.5 N2 O3P 1 21/c 116.298; 11.852; 9.939
90; 90.99; 90		1919.6Ma, Weiwei; Fang, Jie; Ren, Jun; Wang, Zhongwen
Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons.
Organic letters, 2015, 17, 4180-4183
1555164 CIFC11 H6 Cl2 O SP n m a11.6812; 6.6839; 13.6312
90; 90; 90		1064.3Wang, Ting; An, Zhenyu; Qi, Zhenjie; Zhuang, Daijiao; Chang, Aosheng; Yang, Yunxia; Yan, Rulong
Ring-opening/annulation reaction of cyclopropyl ethanols: concise access to thiophene aldehydes via C–S bond formation
Organic Chemistry Frontiers, 2019, 6, 3705
1555165 CIFC17 H17 Br O5P b c a11.48; 10.279; 26.181
90; 90; 90		3089.4Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
1555166 CIFC28 H24 Cl N3 O4 SP 1 21 19.5954; 12.6894; 11.2412
90; 112.927; 90		1260.6Zhang, Haoran; Li, Shiwu; Kang, Qiang; Du, Yu
Chiral-at-metal rhodium(iii) complex catalyzed enantioselective synthesis of C2-substituted benzofuran derivatives
Organic Chemistry Frontiers, 2019, 6, 3683
1555167 CIFC18 H20 O5P 1 21/c 110.526; 19.394; 7.8119
90; 96.58; 90		1584.2Wang, Zhenjun; Chen, Shuai; Ren, Jun; Wang, Zhongwen
Cooperative Photo-/Lewis Acid Catalyzed Tandem Intramolecular [3 + 2] Cross-Cycloadditions of Cyclopropane 1,1-Diesters with α,β-Unsaturated Carbonyls for Medium-Sized Carbocycles.
Organic letters, 2015, 17, 4184-4187
1555168 CIFC19 H18 N2 O6 SiC 1 c 110.8289; 10.4035; 17.1866
90; 103.19; 90		1885.14Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R.
Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes
Organic Chemistry Frontiers, 2019, 6, 3793
1555169 CIFC25 H22 N2 O6 SiP 21 21 215.9864; 18.2027; 21.5323
90; 90; 90		2346.35Vale, João R.; Valkonen, Arto; Afonso, Carlos A. M.; Candeias, Nuno R.
Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes
Organic Chemistry Frontiers, 2019, 6, 3793
1555170 CIFC22 H26 O7P 21 21 219.136; 10.6809; 42.2825
90; 90; 90		4126Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555171 CIFC23 H28 O7P 21 21 218.5586; 9.2119; 27.3349
90; 90; 90		2155.11Bera, Srikrishna; Daniliuc, Constantin G.; Studer, Armido
Enantioselective Synthesis of Substituted δ-Lactones by Cooperative Oxidative N-Heterocyclic Carbene and Lewis Acid Catalysis.
Organic letters, 2015, 17, 4940-4943
1555172 CIFC34 H30 N2 O6P 1 21/n 111.4637; 45.4434; 12.0124
90; 116.324; 90		5608.9Yan, Jianming; Tay, Guan Liang; Neo, Cuien; Lee, Bo Ra; Chan, Philip Wai Hong
Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines.
Organic letters, 2015, 17, 4176-4179
1555173 CIFC24 H32 O5C 1 2 125.9119; 7.4654; 11.5725
90; 107.999; 90		2129.06Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao
Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion
Organic Chemistry Frontiers, 2019, 6, 3839
1555174 CIFC22 H30.66667 O4.33333P 21 21 2112.7263; 18.5197; 24.0727
90; 90; 90		5673.6Wang, Jia-Peng; Shu, Yan; Liu, Shi-Xi; Hu, Jun-Tao; Sun, Cheng-Tong; Zhou, Hao; Gan, Dong; Cai, Xue-Yun; Pu, Wei; Cai, Le; Ding, Zhong-Tao
Expanstines A–D: four unusual isoprenoid epoxycyclohexenones generated by Penicillium expansum YJ-15 fermentation and photopromotion
Organic Chemistry Frontiers, 2019, 6, 3839
1555175 CIFC26 H18 N4 O5P -19.141; 10.706; 12.0986
73.26; 68.76; 72.31		1030.1Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555176 CIFC18 H26 O6P 6520.3875; 20.3875; 7.4174
90; 90; 120		2669.99Li, Hong-Tao; Tang, Linhuan; Liu, Tao; Yang, Ruining; Yang, Yabin; Zhou, Hao; Ding, Zhong-Tao
Polyoxygenated meroterpenoids and a bioactive illudalane derivative from a co-culture of Armillaria sp. and Epicoccum sp.
Organic Chemistry Frontiers, 2019, 6, 3847
1555177 CIFC21 H15 N3 O3P 1 21/c 116.334; 13.572; 7.87
90; 104.13; 90		1691.9Miura, Wataru; Hirano, Koji; Miura, Masahiro
Copper-Mediated Oxidative Coupling of Benzamides with Maleimides via Directed C-H Cleavage.
Organic letters, 2015, 17, 4034-4037
1555178 CIFC34 H27.62 N2 O6P -110.4723; 12.7127; 12.7391
113.157; 97.019; 110.996		1385.7Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank
1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties
Organic Chemistry Frontiers, 2019, 6, 3731
1555179 CIFC51 H52 N2 O7P -112.287; 13.2979; 27.85
86.66; 90; 90		4542.7Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank
1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties
Organic Chemistry Frontiers, 2019, 6, 3731
1555180 CIFC32 H28 N2 O6P n a 2132.9549; 12.7486; 24.5123
90; 90; 90		10298.3Chen, Meng-Ting; Zhang, Yang; Vysotsky, Myroslav O.; Lindner, Joachim O.; Li, Meng-Hua; Lin, Mei-Jin; Würthner, Frank
1,1′-Bi(2-naphthol-4,5-dicarboximide)s: blue emissive axially chiral scaffolds with aggregation-enhanced emission properties
Organic Chemistry Frontiers, 2019, 6, 3731
1555181 CIFC24 H19 N2 O2 S2P 1 21/c 18.3103; 22.0934; 11.8386
90; 104.267; 90		2106.56Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang
Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.
Organic letters, 2015, 17, 4188-4191
1555182 CIFC25 H18 O5P 1 21 111.6007; 5.7368; 15.0074
90; 101.62; 90		978.29Zhang, Song; Yu, Xiaojun; Pan, Jianke; Jiang, Chunhui; Zhang, Hongsu; Wang, Tianli
Asymmetric synthesis of spiro-structural 2,3-dihydrobenzofurans via the bifunctional phosphonium salt-promoted [4 + 1] cyclization of ortho-quinone methides with α-bromoketones
Organic Chemistry Frontiers, 2019, 6, 3799
1555183 CIFC48 H38 Cl2 N4 O4 S4P 21 21 2112.652; 19.153; 22.403
90; 90; 90		5428.8Chen, Xiang; Zhang, Jun-Qi; Yin, Shao-Jie; Li, Hai-Yan; Zhou, Wei-Qun; Wang, Xing-Wang
Asymmetric Construction of Spiro[thiopyranoindole-benzoisothiazole] Scaffold via a Formal [3 + 3] Spiroannulation.
Organic letters, 2015, 17, 4188-4191
1555184 CIFC16 H19 N O3P 1 21/n 111.4043; 9.8807; 25.367
90; 93.04; 90		2854.4Zhong, Jiaxin; He, Haibing; Gao, Shuanhu
Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids
Organic Chemistry Frontiers, 2019, 6, 3781
1555185 CIFC26 H37 N O8C 1 c 124.4812; 7.9863; 25.3899
90; 103.221; 90		4832.51Zhong, Jiaxin; He, Haibing; Gao, Shuanhu
Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids
Organic Chemistry Frontiers, 2019, 6, 3781
1555186 CIFC22 H29 N O5P 1 21/c 18.3885; 24.6653; 19.7148
90; 97.294; 90		4046.08Zhong, Jiaxin; He, Haibing; Gao, Shuanhu
Exploration of 1,3-dipolar cycloaddition reactions to construct the core skeleton of Calyciphylline A-type alkaloids
Organic Chemistry Frontiers, 2019, 6, 3781
1555187 CIFC19 H21 Cl2 N O2 SP 21 21 216.1472; 11.724; 27.834
90; 90; 90		2006Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555188 CIFC19 H20 Cl N O2 SP 1 21 110.133; 9.753; 19.638
90; 100.289; 90		1909.6Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555189 CIFC25 H23 N O3 SP 1 21 111.1372; 8.2426; 12.2345
90; 110.187; 90		1054.13Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai
Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals
Organic Chemistry Frontiers, 2019, 6, 3725
1555190 CIFC25 H25 N O4 SC 1 2 126.476; 9.6581; 9.1391
90; 98.974; 90		2308.3Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai
Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals
Organic Chemistry Frontiers, 2019, 6, 3725
1555191 CIFC25 H23 N O3 SP 1 21 18.784; 9.976; 12.349
90; 90.656; 90		1082.1Chen, Ying-Han; Lv, Xue-Jiao; You, Zhi-Hao; Liu, Yan-Kai
Asymmetric organocatalyzed reaction sequence of 2-hydroxy cinnamaldehydes and acyclic N-sulfonyl ketimines to construct diverse chiral bridged polycyclic aminals
Organic Chemistry Frontiers, 2019, 6, 3725
1555192 CIFC19 H20 Cl N O2 SP 21 21 218.434; 9.511; 23.843
90; 90; 90		1913Huang, Ze-Ao; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Stereoselective Synthesis of Enantioenriched 2-Chloro-2-aroylaziridines by Cascade Reaction between Aryl Nitriles, Silyldichloromethanes, and tert-Butanesulfinylimines.
Organic letters, 2015, 17, 4042-4045
1555193 CIFC30 H23 N3 O2 SP 1 21/c 113.65; 9.7451; 19.194
90; 105.2; 90		2463.9Vivek Kumar, Sundaravel; Banerjee, Sonbidya; Punniyamurthy, Tharmalingam
Rh-Catalyzed C–C/C–N bond formation via C–H activation: synthesis of 2H-indazol-2-yl-benzo[a]carbazoles
Organic Chemistry Frontiers, 2019, 6, 3885
1555194 CIFC25 H19 N3 OP 21 21 217.2944; 14.078; 19.047
90; 90; 90		1955.9Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.
Organic letters, 2015, 17, 4066-4069
1555195 CIFC31 H29 N3 O3 SP -19.8054; 11.1916; 13.8588
102.001; 100.882; 107.337		1367.85Wang, Fei; Xu, Pei; Liu, Bei-Bei; Wang, Shun-Yi; Ji, Shun-Jun
Pd-Catalyzed multicomponent reaction of sulfonyl azides, primary amines and methyl α-isocyanoacetates: highly efficient synthesis of tetrasubstituted imidazolone derivatives
Organic Chemistry Frontiers, 2019, 6, 3754
1555196 CIFC21 H19 N3 OP b c a12.7097; 15.6515; 17.3613
90; 90; 90		3453.6Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro
Copper-Catalyzed Formal [4 + 1] Cycloaddition of Benzamides and Isonitriles via Directed C-H Cleavage.
Organic letters, 2015, 17, 4066-4069
1555197 CIFC22 H34 N4 O9P -19.7492; 10.793; 12.316
106.75; 97.22; 95.45		1219.3Jia, Yan-Lai; Wei, Mei-Yan; Chen, Hai-Yan; Guan, Fei-Fei; Wang, Chang-Yun; Shao, Chang-Lun
(+)- and (-)-Pestaloxazine A, a Pair of Antiviral Enantiomeric Alkaloid Dimers with a Symmetric Spiro[oxazinane-piperazinedione] Skeleton from Pestalotiopsis sp.
Organic letters, 2015, 17, 4216-4219
1555198 CIFC17 H14 N2 O2P 1 21/c 18.4028; 8.4685; 18.8231
90; 91.121; 90		1339.18Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555199 CIFC23 H18 N2 O2P n a 2128.7181; 16.094; 7.4702
90; 90; 90		3452.65Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555200 CIFC21 H16 N2 O2P b c a8.899; 16.027; 21.774
90; 90; 90		3106Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555201 CIFC35 H24 N4 O3P 1 21/c 114.7127; 13.2097; 27.114
90; 97.327; 90		5226.6Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555202 CIFC21 H16 N2 O2P b c a16.535; 8.4288; 22.1228
90; 90; 90		3083.3Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555203 CIFC28 H19 N3 O2P -18.36; 9.772; 13.225
79.646; 71.931; 81.249		1005Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555204 CIFC23 H16 Br2 N2 O2P 1 21/n 114.667; 9.231; 15.139
90; 107.187; 90		1958.2Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555205 CIFC25 H18 N2 O2P b c n18.714; 15.974; 12.0964
90; 90; 90		3616.1Wössner, Jan S.; Grenz, David C.; Kratzert, Daniel; Esser, Birgit
Tuning the optical properties of spiro-centered charge-transfer dyes by extending the donor or acceptor part
Organic Chemistry Frontiers, 2019, 6, 3649
1555206 CIFC26 H24 N4 O4C 1 c 19.0718; 20.806; 12.975
90; 107.07; 90		2341.1Liu, Honglei; Yuan, Chunhao; Wu, Yang; Xiao, Yumei; Guo, Hongchao
Sc(OTf)3-Catalyzed [3 + 3] Cycloaddition of Cyclopropane 1,1-Diesters with Phthalazinium Dicyanomethanides.
Organic letters, 2015, 17, 4220-4223
1555207 CIFC42 H22 F6P -19.9256; 11.9918; 12.9082
90.335; 100.557; 103.488		1466.85Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555208 CIFC42 H22 F6P b c a9.5341; 17.1742; 34.8068
90; 90; 90		5699.3Rao, M. Rajeswara; Black, Hayden T.; Perepichka, Dmitrii F.
Synthesis and Divergent Electronic Properties of Two Ring-Fused Derivatives of 9,10-Diphenylanthracene.
Organic letters, 2015, 17, 4224-4227
1555209 CIFC44.4 H38.4 N1.2 S1.8P 62 2 228.8585; 28.8585; 37.617
90; 90; 120		27130.8Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K.
Core-modified 48π and 42π decaphyrins: syntheses, properties and structures
Organic Chemistry Frontiers, 2019, 6, 3746
1555210 CIFC42 H34 N4 S3P -18.69725; 10.9283; 20.5323
84.0758; 88.6243; 67.6514		1795.05Ghosh, Arindam; Dash, Syamasrit; Srinivasan, A.; Suresh, C. H.; Peruncheralathan, S.; Chandrashekar, Tavarekere K.
Core-modified 48π and 42π decaphyrins: syntheses, properties and structures
Organic Chemistry Frontiers, 2019, 6, 3746
1555211 CIFC65 H65 Cl3 N4 O6 ZnP 4318.5406; 18.5406; 21.1268
90; 90; 90		7262.4Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555212 CIFC24 H24 O3P 1 21/c 110.0558; 10.1395; 18.5575
90; 98.819; 90		1869.77Jiao, Meng-Jie; Liu, Dan; Hu, Xiu-Qin; Xu, Peng-Fei
Photocatalytic decarboxylative [2 + 2 + 1] annulation of 1,6-enynes with N-hydroxyphthalimide esters for the synthesis of indene-containing polycyclic compounds
Organic Chemistry Frontiers, 2019, 6, 3834
1555213 CIFC70 H77 Cl1.5 N4 O5 ZnC 1 2/c 139.3331; 14.7758; 28.6914
90; 131.696; 90		12450.8Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555214 CIFC67 H71 N4 O5 ZnP -116.9996; 24.3355; 32.7331
89.3681; 83.194; 89.522		13444.9Zhou, Zaichun; Zhou, Xiaochun; Liu, Qiuhua; Zhang, Xi; Liu, Haomin
Fixation of Zinc(II) Ion to Dioxygen in a Highly Deformed Porphyrin: Implications for the Oxygen Carrier Mechanism of Distorted Heme.
Organic letters, 2015, 17, 4078-4081
1555215 CIFC26 H22 Br F3 N4 O4P 1 21/c 19.2204; 24.665; 11.584
90; 105.11; 90		2543.4Zhao, Hong-Wu; Guo, Jia-Ming; Wang, Li-Ru; Ding, Wan-Qiu; Tang, Zhe; Song, Xiu-Qing; Wu, Hui-Hui; Fan, Xiao-Zu; Bi, Xiao-Fan
Diastereoselective formal [3 + 3] cycloaddition of isatin-based α-(trifluoromethyl)imines with N,N′-dialkyloxyureas
Organic Chemistry Frontiers, 2019, 6, 3891
1555216 CIFC14 H11 N3C 1 2/c 114.857; 12.127; 13.289
90; 106.898; 90		2290.9Jia, Feng-Cheng; Zhou, Zhi-Wen; Xu, Cheng; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Expeditious Synthesis of 2-Phenylquinazolin-4-amines via a Fe/Cu Relay-Catalyzed Domino Strategy.
Organic letters, 2015, 17, 4236-4239
1555217 CIFC63.25 H86 Na5 O29.95 S5P -112.15; 12.226; 26.113
99.044; 97.039; 99.079		3739.3Pisagatti, Ilenia; Barbera, Lucia; Gattuso, Giuseppe; Parisi, Melchiorre F.; Geremia, Silvano; Hickey, Neal; Notti, Anna
Guest-length driven high fidelity self-sorting in supramolecular capsule formation of calix[5]arenes in water
Organic Chemistry Frontiers, 2019, 6, 3804
1555218 CIFC33 H23 Cl3 N2 O2P 1 21 19.07268; 11.9732; 13.4535
90; 106.945; 90		1397.99Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555219 CIFC32.5 H26 N2 O3.5P 21 21 211.4574; 24.0028; 9.1294
90; 90; 90		2510.67Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555220 CIFC34 H24 O2P 21 21 211.1679; 24.1852; 9.1499
90; 90; 90		2471.37Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555221 CIFC32 H22.67 N2 O2.33P 21 21 2110.41941; 18.297; 36.8632
90; 90; 90		7027.75Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555222 CIFC32 H22 N2 O2P 21 21 217.9491; 16.7592; 18.1848
90; 90; 90		2422.6Takaishi, Kazuto; Suzuki, Jun; Yabe, Tatsuya; Asano, Hikaru; Nishikawa, Michihiro; Hashizume, Daisuke; Muranaka, Atsuya; Uchiyama, Masanobu; Yokoyama, Akihiro
Conformational and Optical Characteristics of Unidirectionally Twisted Binaphthyl-Bipyridyl Cyclic Dyads.
Organic letters, 2015, 17, 4098-4101
1555223 CIFC245 H138 Cl10 F24 N8 O32 S8P -116.057; 18.336; 18.879
79.909; 74.398; 79.264		5214Węcławski, Marek K; Meiling, Till T.; Leniak, Arkadiusz; Cywiński, Piotr J; Gryko, Daniel T.
Planar, Fluorescent Push-Pull System That Comprises Benzofuran and Iminocoumarin Moieties.
Organic letters, 2015, 17, 4252-4255
1555224 CIFC41 H36 N2 O9P 1 21/c 119.0503; 11.68507; 14.8134
90; 92.939; 90		3293.19Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
1555225 CIFC40 H32 N2 O9P b c a13.9815; 16.6793; 26.5582
90; 90; 90		6193.4Sai, Chun-Mei; Li, Da-Hong; Xue, Chun-Mei; Wang, Kai-Bo; Hu, Ping; Pei, Yue-Hu; Bai, Jiao; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming
Two Pairs of Enantiomeric Alkaloid Dimers from Macleaya cordata.
Organic letters, 2015, 17, 4102-4105
1555226 CIFC28 H24 N2 O3 SP 21 21 218.9629; 14.1297; 18.6198
90; 90; 90		2358.1Wang, Linqing; Yang, Dongxu; Li, Dan; Liu, Xihong; Zhao, Qian; Zhu, Ranran; Zhang, Bangzhi; Wang, Rui
Catalytic Asymmetric [3 + 2] Cyclization Reactions of 3-Isothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst.
Organic letters, 2015, 17, 4260-4263
1555227 CIFC24 H25 F3 I N O4 SP 1 21/c 113.4658; 20.2837; 19.439
90; 100.921; 90		5213.3Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555228 CIFC6 H13 N O3P 418.8749; 8.8749; 20.4808
90; 90; 90		1613.1Chung, Ryan; Hein, Jason E.
Automated solubility and crystallization analysis of non-UV active compounds: integration of evaporative light scattering detection (ELSD) and robotic sampling
Reaction Chemistry & Engineering, 2019, 4, 1674
1555229 CIFC24 H26 F2 I N O4 SP 1 21/n 112.121; 15.7186; 25.7853
90; 91.321; 90		4911.4Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555230 CIFC23 H25 F2 I N2 O4 SP n a 2124.1416; 10.1959; 20.5376
90; 90; 90		5055.2Wang, Yu-Qi; He, Yu-Tao; Zhang, Lu-Lu; Wu, Xin-Xing; Liu, Xue-Yuan; Liang, Yong-Min
Palladium-Catalyzed Radical Cascade Iododifluoromethylation/Cyclization of 1,6-Enynes with Ethyl Difluoroiodoacetate.
Organic letters, 2015, 17, 4280-4283
1555231 CIFC16 H26 O6P 1 21 16.5502; 13.639; 9.1291
90; 91.21; 90		815.4Hwang, In Hyun; Swenson, Dale C.; Gloer, James B.; Wicklow, Donald T.
Pestaloporonins: Caryophyllene-Derived Sesquiterpenoids from a Fungicolous Isolate of Pestalotiopsis sp.
Organic letters, 2015, 17, 4284-4287
1555232 CIFC19 H21 Br Cl N O2P 1 21 19.5181; 11.3448; 18.2344
90; 105.143; 90		1900.6Monasterolo, Claudio; Müller-Bunz, Helge; Gilheany, Declan G.
Very short highly enantioselective Grignard synthesis of 2,2-disubstituted tetrahydrofurans and tetrahydropyrans.
Chemical science, 2019, 10, 6531-6538
1555233 CIFC22 H36 O6 SiP 1 21 16.395; 46.881; 8.2621
90; 111.164; 90		2309.9Clark, J. Stephen; Romiti, Filippo; Sieng, Bora; Paterson, Laura C.; Stewart, Alister; Chaudhury, Subhabrata; Thomas, Lynne H.
Synthesis of the A-D Ring System of the Gambieric Acids.
Organic letters, 2015, 17, 4694-4697
1555234 CIFC31 H30 F3 Ir N6P -114.228; 15.407; 16.166
86.526; 65.199; 85.672		3206Na, Hanah; Cañada, Louise M; Wen, Zhili; I-Chia Wu, Judy; Teets, Thomas S.
Mixed-carbene cyclometalated iridium complexes with saturated blue luminescence.
Chemical science, 2019, 10, 6254-6260
1555235 CIFC39 H34 F3 Ir N6C 1 2/c 127.27; 20.718; 14.832
90; 116.007; 90		7531Na, Hanah; Cañada, Louise M; Wen, Zhili; I-Chia Wu, Judy; Teets, Thomas S.
Mixed-carbene cyclometalated iridium complexes with saturated blue luminescence.
Chemical science, 2019, 10, 6254-6260
1555236 CIFC14 H17 F O2P 21 21 215.8616; 11.0435; 18.6965
90; 90; 90		1210.27Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555237 CIFC23 H23 F N2 O6P -17.9045; 11.1779; 11.7527
91.21; 92.807; 94		1034.33Navuluri, Chandrasekhar; Charette, André B
Diastereoselective Fluorocyclopropanation of Chiral Allylic Alcohols Using an α-Fluoroiodomethylzinc Carbenoid.
Organic letters, 2015, 17, 4288-4291
1555238 CIFC26 H54 N2 O2 Zn2P 42/n :212.3523; 12.3523; 19.4557
90; 90; 90		2968.54Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz
Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO.
Chemical science, 2019, 10, 7149-7155
1555239 CIFC30 H46 N2 O2 Zn2P 1 21/c 19.4169; 30.0759; 10.6586
90; 106.582; 90		2893.2Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz
Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO.
Chemical science, 2019, 10, 7149-7155
1555240 CIFC30 H46 N2 O2 ZnP 1 21/c 110.525; 22.503; 12.296
90; 95.834; 90		2897.15Budny-Godlewski, Krzysztof; Justyniak, Iwona; Leszczyński, Michał K; Lewiński, Janusz
Mechanochemical and slow-chemistry radical transformations: a case of diorganozinc compounds and TEMPO.
Chemical science, 2019, 10, 7149-7155
1555241 CIFC76 H48 O4C 2 2 219.5716; 40.233; 14.5609
90; 90; 90		5607.3Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555242 CIFC26 H18 O2C 2 2 219.6233; 28.1324; 14.4388
90; 90; 90		3908.97Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555243 CIFC26 H18 Br2 O2C 2 2 219.5385; 16.362; 14.106
90; 90; 90		2201.5Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555244 CIFC76 H78 O16 S4P 43 21 213.3557; 13.3557; 44.138
90; 90; 90		7873.1Chen, Jing-Xing; Han, Jian-Wei; Wong, Henry N. C.
Synthesis and Chiroptical Properties of Double-Helical (M)- and (P)-o-Oligophenylenes.
Organic letters, 2015, 17, 4296-4299
1555245 CIFC21 H19 Cl O3P 1 21/c 120.4519; 8.3981; 29.0733
90; 133.17; 90		3641.9Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555246 CIFC21 H19 Br O3P 1 21/c 19.2815; 26.184; 8.2635
90; 114.173; 90		1832.2Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555247 CIFC21 H19 F O3P 1 21/n 18.0324; 10.4173; 21.4761
90; 98.076; 90		1779.2Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555248 CIFC18 H12 O2P 1 21/c 111.0083; 17.6321; 6.9894
90; 98.387; 90		1342.1Yu, Zhunzhun; Li, Yongfeng; Zhang, Peichao; Liu, Lu; Zhang, Junliang
Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters.
Chemical science, 2019, 10, 6553-6559
1555249 CIFC40 H34 Br N3 O3P 21 21 2112.8306; 13.8096; 19.054
90; 90; 90		3376.1Jing, Changcheng; Xing, Dong; Hu, Wenhao
Catalytic Asymmetric Four-Component Reaction for the Rapid Construction of 3,3-Disubstituted 3-Indol-3'-yloxindoles.
Organic letters, 2015, 17, 4336-4339
1555250 CIFC19 H18 O2P -18.2948; 9.5359; 10.0158
75.291; 74.899; 86.594		739.79Lu, Qingquan; Mondal, Shobhan; Cembellín, Sara; Greßies, Steffen; Glorius, Frank
Site-selective C-H activation and regiospecific annulation using propargylic carbonates.
Chemical science, 2019, 10, 6560-6564
1555251 CIFC18 H16 O SP 1 21/n 15.3543; 15.615; 17.226
90; 93.57; 90		1437.4Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555252 CIFC17 H15 Co0.5 O3P 1 21/n 19.6119; 16.0078; 12.0749
90; 94.068; 90		1853.23Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Shaw, Bikash Kumar; Vaidya, Shefali; Pariyar, Anand; Vijaykumar, Gonela; Adhikari, Debashis; Mandal, Swadhin K.
Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction.
Chemical science, 2019, 10, 7433-7441
1555253 CIFC13 H8.64 O2P c c n7.379; 14.8543; 16.8845
90; 90; 90		1850.7Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Shaw, Bikash Kumar; Vaidya, Shefali; Pariyar, Anand; Vijaykumar, Gonela; Adhikari, Debashis; Mandal, Swadhin K.
Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction.
Chemical science, 2019, 10, 7433-7441
1555254 CIFC24 H16 O SP 1 21/c 19.1038; 11.532; 16.523
90; 101.54; 90		1699.6Zhao, Peng; Liu, Yu; Xi, Chanjuan
MeOTf-Induced Carboannulation of Isothiocyanates and Aryl Alkynes with C═S Bond Cleavage: Access to Indenones.
Organic letters, 2015, 17, 4388-4391
1555255 CIFC12 H14 B2 F8 Fe N6 O2C m c e7.243; 12.882; 23.908
90; 90; 90		2230.7Resines-Urien, Esther; Burzurí, Enrique; Fernandez-Bartolome, Estefania; García García-Tuñón, Miguel Ángel; de la Presa, Patricia; Poloni, Roberta; Teat, Simon J.; Costa, Jose Sanchez
A switchable iron-based coordination polymer toward reversible acetonitrile electro-optical readout.
Chemical science, 2019, 10, 6612-6616
1555256 CIFC21 H30 O4 SiP 1 21/c 115.86; 8.9849; 32.138
90; 117.571; 90		4059.6Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555257 CIFC20 H28 O3 SiC 1 2/c 134.403; 6.7764; 16.1333
90; 92.333; 90		3758Khatri, Buddha B.; Sieburth, Scott McN
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Organic letters, 2015, 17, 4360-4363
1555258 CIFC9 H5 Cl2 N3 SP b c a6.9189; 13.8264; 21.5767
90; 90; 90		2064.1Kalogirou, Andreas S.; Manoli, Maria; Koutentis, Panayiotis A.
Synthesis of N-Aryl-3,5-dichloro-4H-1,2,6-thiadiazin-4-imines from 3,4,4,5-Tetrachloro-4H-1,2,6-thiadiazine.
Organic letters, 2015, 17, 4118-4121
1555259 CIFC14 H20 O16.75P n -3 :211.4074; 11.4074; 11.4074
90; 90; 90		1484.43Cui, Peng; McMahon, David P.; Spackman, Peter R.; Alston, Ben M.; Little, Marc A.; Day, Graeme M.; Cooper, Andrew I.
Mining predicted crystal structure landscapes with high throughput crystallisation: old molecules, new insights
Chemical Science, 2019, 10, 9988
1555260 CIFC15 H18 O8.25I 41/a :216.4008; 16.4008; 22.397
90; 90; 90		6024.5Cui, Peng; McMahon, David P.; Spackman, Peter R.; Alston, Ben M.; Little, Marc A.; Day, Graeme M.; Cooper, Andrew I.
Mining predicted crystal structure landscapes with high throughput crystallisation: old molecules, new insights
Chemical Science, 2019, 10, 9988

Blue left arrow Blue left arrow First | Blue left arrow Previous 500 | of 1057 | Next 500 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.