Crystallography Open Database

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7157726 CIFC17 H23 F2 N O3P 1 21 19.0751; 6.1933; 15.1581
90; 98.79; 90
841.95Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157727 CIFC17 H23 F2 N O3P 1 21/c 16.0625; 22.0365; 12.8581
90; 90.522; 90
1717.7Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157728 CIFC24 H21 N3 O2P 1 21/c 19.5144; 13.3582; 16.0144
90; 102.194; 90
1989.43Tang, Shi-Biao; Fu, Xiao-Pan; Wu, Gao-Rong; Zhang, Li-Li; Deng, Ke-Zuan; Yang, Jin-Yue; Xia, Cheng-Cai; Ji, Ya-Fei
Rhodium(III)-catalyzed C4-amidation of indole-oximes with dioxazolones <i>via</i> C-H activation.
Organic & biomolecular chemistry, 2020, 18, 7922-7931
7157729 CIFC12.8 H8.8 N0.4 O0.4P -19.6741; 10.8198; 12.5635
69.234; 89.878; 72.178
1162.2Xu, Fen; Zhu, Wen-Jing; Wang, Juan; Ma, Qi; Shen, Li-Jing
Rhodium-catalyzed synthesis of substituted isoquinolones <i>via</i> a selective decarbonylation/alkyne insertion cascade of phthalimides.
Organic & biomolecular chemistry, 2020, 18, 8219-8223
7157730 CIFC16 H20 O6C 1 2 18.1628; 13.0501; 13.9274
90; 103.346; 90
1443.55Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157731 CIFC16 H20 O5P 21 21 217.2801; 9.9611; 18.9298
90; 90; 90
1372.75Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157732 CIFC16 H20 O5P 21 21 216.8403; 10.54278; 7.78736
90; 90; 90
1382.6Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157733 CIFC16 H18 O3P 21 21 217.1617; 9.7401; 18.6984
90; 90; 90
1304.32Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157734 CIFC19 H20 Cl N O5P 1 21 19.6261; 6.61723; 14.2237
90; 98.0027; 90
897.2Romaniszyn, Marta; Sieroń, Lesław; Albrecht, Łukasz
Asymmetric vinylogous Michael addition of 5-substituted-furan-2(3<i>H</i>)-ones to an α,β-unsaturated-γ-lactam.
Organic & biomolecular chemistry, 2020, 18, 8633-8637
7157735 CIFC40 H52 O11P b c n17.1752; 8.82114; 24.8611
90; 90; 90
3766.58Choo, Yvonne S. L.; Giamberini, Marta; Antonio, José; Waddell, Paul G.; Benniston, Andrew C.
Functionalized fluorescent terephthalate monomers and their attempted polyester formation.
Organic & biomolecular chemistry, 2020, 18, 8735-8745
7157736 CIFC H N OP b c a12.9152; 15.907; 18.038
90; 90; 90
3705.8Liu, Siyuan; Wang, Hang; Wang, Baomin
Catalyst-free construction of spiro [benzoquinolizidine-chromanones] <i>via</i> a tandem condensation/1,5-hydride transfer/cyclization process.
Organic & biomolecular chemistry, 2020, 18, 8839-8843
7157737 CIFC20 H14 N2 OP b c a8.3127; 17.1849; 20.9916
90; 90; 90
2998.71Jaspal, Sonam; Shinde, Vikki N.; Meena, Neha; Nipate, Dhananjay S.; Rangan, Krishnan; Kumar, Anil
Metal-free benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acids.
Organic & biomolecular chemistry, 2020, 18, 9072-9080
7157738 CIFC23 H17 N5 O2P 1 21/n 111.158; 11.434; 15.708
90; 96.925; 90
1989.4Ge, Junying; Ding, Qiuping; Yang, Man; He, Tian; Peng, Yiyuan
Copper and manganese co-mediated cascade aza-Michael addition/cyclization and azidation of 1,3-enynes: regioselective synthesis of fully substituted azido pyrroles.
Organic & biomolecular chemistry, 2020, 18, 8908-8915
7157739 CIFC18 H14 Cl N O3C 1 2/c 129.8793; 7.7831; 12.7135
90; 93.634; 90
2950.6Yugandar, Somaraju; Morita, Taiki; Nakamura, Hiroyuki
Rhodium(III)-catalysed decarboxylative C-H functionalization of isoxazoles with alkenes and sulfoxonium ylides.
Organic & biomolecular chemistry, 2020, 18, 8625-8628
7157740 CIFC26 H24 F N3P 21 21 215.6056; 17.422; 22.161
90; 90; 90
2164.3Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157741 CIFC21 H16 F N3P b c a9.2995; 9.7287; 37.4385
90; 90; 90
3387.1Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157742 CIFC24 H20 F N3 OP 1 21 15.4142; 20.89; 8.3858
90; 92.126; 90
947.8Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157743 CIFC37 H29 N O4P 110.7714; 11.3185; 13.3343
66.429; 80.647; 75.079
1436.53Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157744 CIFC36 H26 N2 O2P 3112.9632; 12.9632; 16.2424
90; 90; 120
2363.77Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157745 CIFC36 H32 N2 O2P 21 21 219.3208; 15.9714; 19.0521
90; 90; 90
2836.21Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157746 CIFC7 H7 Br N2 OP -13.8839; 8.7474; 22.667
81.742; 88.786; 85.859
760.07Li, Yibiao; Huang, Shuo; Li, Jiaming; Li, Jian; Ji, Xiaoliang; Liu, Jiasheng; Chen, Lu; Peng, Shiyong; Zhang, Kun
Access to 2-pyridinylamide and imidazopyridine from 2-fluoropyridine and amidine hydrochloride
Organic & Biomolecular Chemistry, 2020, 18, 9292-9299
7157747 CIFC12 H19 N5 O4P 1 21/c 117.8252; 7.4804; 10.9523
90; 105.159; 90
1409.56Nakaike, Yumi; Yoshida, Yusuke; Yokoyama, Soichi; Ito, Akitaka; Nishiwaki, Nagatoshi
Synthesis and intramolecular ring transformation of N,N′-dialkylated 2,6,9-triazabicyclo[3.3.1]nonadienes
Organic & Biomolecular Chemistry, 2020, 18, 9109-9116
7157748 CIFC20 H19 N5 O4P 1 21/n 114.4032; 9.8582; 19.916
90; 140.02; 90
1817Nakaike, Yumi; Yoshida, Yusuke; Yokoyama, Soichi; Ito, Akitaka; Nishiwaki, Nagatoshi
Synthesis and intramolecular ring transformation of N,N′-dialkylated 2,6,9-triazabicyclo[3.3.1]nonadienes
Organic & Biomolecular Chemistry, 2020, 18, 9109-9116
7157749 CIFC18 H17 N O4 SC 1 c 113.738; 15.885; 7.706
90; 111.13; 90
1569Ahn, Hye-In; Park, Jong-Un; Xuan, Zi; Kim, Ju Hyun
Pd-Catalyzed asymmetric [5 + 2] cycloaddition of vinylethylene carbonates and cyclic imines: access to N-fused 1,3-oxazepines.
Organic & biomolecular chemistry, 2020, 18, 9826-9830
7157750 CIFC11 H13 Cl N4 OP 14.4944; 5.4263; 12.2978
97.735; 94.192; 92.2
296.04Zhang, Yanhua; Lin, Yun; Hou, Qianqian; Liu, Xi; Pricl, Sabrina; Peng, Ling; Xia, Yi
Novel aryltriazole acyclic C-azanucleosides as anticancer candidates.
Organic & biomolecular chemistry, 2020, 18, 9689-9699
7157751 CIFC28 H25 Cl3 N2 O4 SP 1 21/n 19.9981; 15.1043; 18.6398
90; 92.173; 90
2812.85Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157752 CIFC29 H27 Cl3 N2 O4 SC 1 2/c 126.0749; 9.8982; 23.541
90; 105.383; 90
5858.1Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157753 CIFC21 H19 Cl N2 O3C 1 2/c 122.788; 9.824; 19.984
90; 123.49; 90
3731.1Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157759 CIFC16 H18 Cl N O6P 1 21/a 111.042; 8.8933; 16.9598
90; 95.377; 90
1658.12Bakthadoss, Manickam; Mushaf, Mohammad
Intramolecular [3 + 2] nitrone cycloaddition reaction: highly regio and diastereoselective synthesis of bicyclo[3.2.1]octane scaffolds.
Organic & biomolecular chemistry, 2020, 18, 9653-9659
7157760 CIFC23 H17 N OP 1 21/n 18.8725; 11.6847; 16.8773
90; 102.266; 90
1709.77Shen, Bing-Xue; Min, Xiang-Ting; Hu, Yan-Cheng; Qian, Lei-Lei; Yang, Sa-Na; Wan, Boshun; Chen, Qing-An
Copper-catalyzed boroacylation of allenes to access tetrasubstituted vinylboronates
Organic & Biomolecular Chemistry, 2020, 18, 9253-9260
7157761 CIFC27 H18 N2P 1 21/n 111.8524; 12.1284; 14.3084
90; 107.05; 90
1966.4Huang, Jian; Fu, Yang; Deng, Zhihong; Chen, Wei; Song, Zhibin; Peng, Yiyuan
Rhodium-catalyzed oxidative annulation of 1H-indazoles with alkynes for the synthesis of indazolo[3,2-a]isoquinolines via C-H bond functionalization.
Organic & biomolecular chemistry, 2020, 18, 9863-9872
7157762 CIFC26 H21 Br O5P 1 21/n 111.6835; 10.2297; 18.6723
90; 101.857; 90
2184.07Wang, Ru-Bing; Ren, Xiao-Dong; He, Jie; Zhu, Shan-Shan; Xie, Hui-Ru; Su, Guo-Zhu; Ma, Shuang-Gang; Yu, Shi-Shan
Burchellin and its stereoisomers: total synthesis, structural elucidation and antiviral activity
Organic & Biomolecular Chemistry, 2020, 18, 9081-9087
7157764 CIFC30 H26 N0.25 O4P 1 21/c 110.5825; 10.9351; 20.533
90; 94.269; 90
2369.5Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157765 CIFC152 H108 Cl12 N8 O8 SI 41/a :226.6744; 26.6744; 18.1796
90; 90; 90
12935.2Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157766 CIFC33 H21 Cl3 N2 O4P 1 21/c 114.0142; 21.038; 9.3503
90; 90.176; 90
2756.74Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157767 CIFC22 H18 Br2 Cl N O3P -18.1923; 10.0872; 13.952
75.123; 88.61; 78.866
1092.9Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157768 CIFC22 H19 Br Cl N O3P 1 21/n 115.6584; 7.2134; 19.131
90; 102.956; 90
2105.8Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157769 CIFC25 H27 N O4P 1 21/c 110.129; 15.539; 15.252
90; 105.482; 90
2313Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157770 CIFC23 H21 Br Cl N O3C 1 2/c 124.318; 9.2383; 20.24
90; 96.433; 90
4518.4Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157771 CIFC39 H53 Br N4 O4 Si3 ZnP -19.3441; 13.5093; 16.7025
98.858; 102.47; 91.92
2029.23Hayashi, Satoshi; Takamatsu, Rina; Takeda, Shiori; Noji, Masahiro; Takanami, Toshikatsu
Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins.
Organic & biomolecular chemistry, 2020, 18, 9791-9795
7157772 CIFC43 H39 N3 O8C 1 2/c 141.0905; 12.1637; 21.1598
90; 134.872; 90
7495Li, Chen-Yi; Xiang, Min; Song, Xiang-Jia; Zou, Ying; Huang, Zhi-Cheng; Li, Xia; Tian, Fang; Wang, Li-Xin
A base-catalyzed domino reaction between isoindigos and α-alkylidene succinimides-convenient preparation of highly steric bispirooxindoles.
Organic & biomolecular chemistry, 2020, 18, 9511-9515
7157773 CIFC17 H19 N O3 SP 15.9286; 8.2863; 8.6201
109.21; 90.208; 103.829
386.74Yang, Shuang; Chen, Yuhang; Yuan, Zidan; Bu, Feiyu; Jiang, Cheng; Ding, Zhenhua
Divergent synthesis of oxazolidines and morpholines <i>via</i> PhI(OAc)<sub>2</sub>-mediated difunctionalization of alkenes.
Organic & biomolecular chemistry, 2020, 18, 9873-9882
7157780 CIFC12 H7 N3 SP 1 n 116.216; 8.5645; 16.5649
90; 117.934; 90
2032.52Yang, Zhen; He, Jing; Wei, Yueting; Li, Weiwei; Liu, Ping; Zhao, Jixing; Wei, Yu
NCS-promoted thiocyanation and selenocyanation of pyrrolo[1,2-a]quinoxalines
Organic & Biomolecular Chemistry, 2020, 18, 9088-9094
7157781 CIFC26 H28 O8P -18.3229; 10.5201; 13.8336
88.816; 73.989; 76.976
1133.19Liu, Hongxin; Chen, Shanchong; Zhang, Xiao; Dong, Chunmao; Chen, Yuchan; Liu, Zhaoming; Tan, Haibo; Zhang, Weimin
Structural elucidation, total synthesis, and cytotoxic activity of effphenol A
Organic & Biomolecular Chemistry, 2020, 18, 9035-9038
7157782 CIFC33 H32 Br N O6P -110.102; 10.4727; 15.726
104.702; 94.205; 109.963
1489Jaiswal, Manish K.; Singh, Bhuvnesh; De, Shreemoyee; Singh, Neetu; Singh, Ravi P.
Stereoselective formal [3 + 3] annulation of 3-alkylidene-2-oxindoles with β,γ-unsaturated α-keto esters.
Organic & biomolecular chemistry, 2020, 18, 9852-9862
7157784 CIFC19 H13 N O4P 1 21/c 14.2074; 12.9179; 27.18
90; 94.001; 90
1473.7He, Xue-Wen; Zhou, Wei; Zhang, Min; Tian, Min-Yi; Wang, Hui-Juan; Tian, You-Ping; Liu, Xiong-Li
Transition-metal-free cascade benzannulations for synthesizing 2-hydroxybenzophenones
Organic & Biomolecular Chemistry, 2020, 18, 9039-9043
7157785 CIFC19 H12 Br N O4P 1 21/c 112.5309; 7.1686; 17.8685
90; 94.845; 90
1599.37He, Xue-Wen; Zhou, Wei; Zhang, Min; Tian, Min-Yi; Wang, Hui-Juan; Tian, You-Ping; Liu, Xiong-Li
Transition-metal-free cascade benzannulations for synthesizing 2-hydroxybenzophenones
Organic & Biomolecular Chemistry, 2020, 18, 9039-9043
7157786 CIFC40 H32P -110.4475; 12.2806; 12.3903
100.338; 99.001; 104.084
1483.14Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157787 CIFC12 H12 Br4P 1 21/c 114.8169; 23.135; 13.2408
90; 94.823; 90
4522.7Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157788 CIFC20 H38 O13 P4C 1 2/c 115.6392; 18.8539; 12.4008
90; 127.729; 90
2892Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157789 CIFC18 H24 O4P -16.9814; 11.397; 11.8876
62.708; 82.487; 73.52
806.04Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157790 CIFC12 H16 O4C 1 2/c 111.6744; 9.2737; 11.2747
90; 114.21; 90
1113.3Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157791 CIFC28 H30 N2P 21 21 216.859; 17.0662; 19.6709
90; 90; 90
2302.6Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157792 CIFC44 H36 N12C 1 2/c 123.8429; 14.4588; 12.002
90; 116.455; 90
3704.3Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157793 CIFC70 H92 O26P 6511.0913; 11.0913; 92.9928
90; 90; 120
9907.06Kikuchi, Takashi; Akita, Keiko; Koike, Hiroki; In, Yasuko; Yamada, Takeshi; Tanaka, Reiko
Carapanins A‒C: new limonoids from andiroba (Carapa guianensis) fruit oil
Organic & Biomolecular Chemistry, 2020, 18, 9268-9274
7157794 CIFC26 H32 O7P 21 21 218.0223; 13.6842; 21.6959
90; 90; 90
2381.75Kikuchi, Takashi; Akita, Keiko; Koike, Hiroki; In, Yasuko; Yamada, Takeshi; Tanaka, Reiko
Carapanins A‒C: new limonoids from andiroba (Carapa guianensis) fruit oil
Organic & Biomolecular Chemistry, 2020, 18, 9268-9274
7157795 CIFC18 H18 N4 O4P 1 21/c 111.1364; 19.9122; 8.5927
90; 107.324; 90
1819Dagar, Anuradha; Kim, Ikyon
Expansion of diazepine heterocyclic chemical space <i>via</i> sequential Knoevenagel condensation-intramolecular aza-Wittig reaction: 2-acyl-4-aryl-5<i>H</i>-pyrrolo[1,2-<i>d</i>][1,4]diazepines.
Organic & biomolecular chemistry, 2020, 18, 9836-9851
7157796 CIFC18 H18 N2 O3P 1 21/n 110.3803; 7.9121; 19.5926
90; 104.061; 90
1560.93Dagar, Anuradha; Kim, Ikyon
Expansion of diazepine heterocyclic chemical space <i>via</i> sequential Knoevenagel condensation-intramolecular aza-Wittig reaction: 2-acyl-4-aryl-5<i>H</i>-pyrrolo[1,2-<i>d</i>][1,4]diazepines.
Organic & biomolecular chemistry, 2020, 18, 9836-9851
7157797 CIFC27 H21 Cl F3 N O7P 1 21/n 113.5978; 14.619; 13.9308
90; 117.095; 90
2465.33Penjarla, Thirupathi Reddy; Kundarapu, Maheshwar; Rangan, Krishnan; Bhattacharya, Anupam
Iodine assisted synthesis of CF<sub>3</sub> appended spirodihydrofuryl/cyclopropyl oxindoles by changing the active methylene sources.
Organic & biomolecular chemistry, 2020, 18, 9623-9631
7157798 CIFC28 H26 F3 N3 O6P 1 21 18.8532; 13.7373; 11.5286
90; 107.761; 90
1335.27Penjarla, Thirupathi Reddy; Kundarapu, Maheshwar; Rangan, Krishnan; Bhattacharya, Anupam
Iodine assisted synthesis of CF<sub>3</sub> appended spirodihydrofuryl/cyclopropyl oxindoles by changing the active methylene sources.
Organic & biomolecular chemistry, 2020, 18, 9623-9631
7157799 CIFC22 H21 N O2 S2P 1 21/n 18.0525; 15.8806; 15.2504
90; 94.189; 90
1945Wu, Jia-Yu; Liao, Wei-Jr; Lin, Xiu-Yi; Liang, Chien-Fu
A facile access to <i>N</i>-sulfonylthioimidates and their use for the transformation to 3,4-dihydroquinazolines.
Organic & biomolecular chemistry, 2020, 18, 8881-8885
7157800 CIFC20 H14 Cl N OP -18.0991; 10.0866; 10.5705
75.779; 69.449; 67.461
740.63Zheng, Jing; He, Xiaojie; Xu, Hong; Liu, Hua; Yang, Weiran
A formal [3 + 2] annulation reaction of propargyl sulfonium compounds and <i>N</i>-ylides: access to pyrrolo[2,1-<i>a</i>]quinolines, pyrrolo[2,1-<i>a</i>]phthalazines and indolizines.
Organic & biomolecular chemistry, 2020, 18, 8867-8875
7157801 CIFC2.5 H2 Cl0.33 O0.67P 1 21/c 111.3742; 18.028; 7.5166
90; 106.736; 90
1476.02Xie, Zhen-Zhen; Deng, Zhi-Xiong; Zheng, Yu; Chen, Yan-Shan; Xiao, Jun-An; Chen, Kai; Xiang, Hao-Yue; Yang, Hua
A phosphine-mediated domino sequence of salicylaldehyde with but-3-yn-2-one: rapid access to chromanone.
Organic & biomolecular chemistry, 2020, 18, 8916-8920
7157802 CIFC24 H19 Br N2 O3 SP -18.1722; 10.5252; 13.3654
80.905; 79.401; 76.274
1089.82Feng, Jiajun; He, Tiantong; Xie, Yuxing; Yu, Yang; Baell, Jonathan B.; Huang, Fei
I<sub>2</sub>-Promoted [4 + 2] cycloaddition of <i>in situ</i> generated azoalkenes with enaminones: facile and efficient synthesis of 1,4-dihydropyridazines and pyridazines.
Organic & biomolecular chemistry, 2020, 18, 9483-9493

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