Crystallography Open Database

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1504046 CIFC16 H25 N O2 SP 1 c 16.119; 13.231; 20.15
90; 91.94; 90
1630Wang, Bing; Wang, Yong-Jun
SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism.
Organic letters, 2009, 11, 3410-3413
1504047 CIFC13 H29 N O3 SP 21 21 216.252; 14.188; 18.445
90; 90; 90
1636.1Wang, Bing; Wang, Yong-Jun
SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism.
Organic letters, 2009, 11, 3410-3413
1504048 CIFC14 H31 N O3 SP 21 21 216.51; 14.258; 18.556
90; 90; 90
1722.4Wang, Bing; Wang, Yong-Jun
SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism.
Organic letters, 2009, 11, 3410-3413
1504049 CIFC42 H42 N6 O5C 1 2/c 124.171; 9.0645; 19.641
90; 123.943; 90
3570Li, Guo-You; Yang, Tao; Luo, Ying-Gang; Chen, Xiao-Zhen; Fang, Dong-Mei; Zhang, Guo-Lin
Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor.
Organic letters, 2009, 11, 3714-3717
1504050 CIFC18 H15 N3 O3P 1 21 17.912; 7.392; 14.05
90; 104.92; 90
794Li, Guo-You; Yang, Tao; Luo, Ying-Gang; Chen, Xiao-Zhen; Fang, Dong-Mei; Zhang, Guo-Lin
Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor.
Organic letters, 2009, 11, 3714-3717
1504051 CIFC17 H28 Cl N2 RhP 1 21/n 16.5715; 18.7963; 13.799
90; 94.439; 90
1699.3Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon
A new route to acyclic diaminocarbenes via lithium-halogen exchange.
Organic letters, 2009, 11, 3274-3277
1504052 CIFC17 H28 Cl Ir N2P 1 21/c 19.8235; 14.9332; 23.221
90; 91.616; 90
3405.1Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon
A new route to acyclic diaminocarbenes via lithium-halogen exchange.
Organic letters, 2009, 11, 3274-3277
1504053 CIFC13 H22 Cl Ir N2P 21 21 217.277; 12.449; 15.738
90; 90; 90
1425.7Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon
A new route to acyclic diaminocarbenes via lithium-halogen exchange.
Organic letters, 2009, 11, 3274-3277
1504054 CIFC22 H16 Br N OP 21 21 216.195; 7.802; 35.452
90; 90; 90
1713.5Li, Yi; Shi, Fu-Qiang; He, Qing-Li; You, Shu-Li
N-heterocyclic carbene-catalyzed cross-coupling of aldehydes with arylsulfonyl indoles.
Organic letters, 2009, 11, 3182-3185
1504055 CIFC11 H17 N O3P -16.6599; 9.8956; 9.9738
108.604; 96.856; 97.248
609.01Meyers, Marvin J.; Muizebelt, Inouk; van Wiltenburg, Jim; Brown, David L.; Thorarensen, Atli
Synthesis of tert-butyl 6-oxo-2-azaspiro[3.3]heptane-2-carboxylate.
Organic letters, 2009, 11, 3523-3525
1504056 CIFC66 H66P 1 21/c 115.0858; 17.9286; 17.9396
90; 94.962; 90
4833.9Zhai, Linyi; Shukla, Ruchi; Rathore, Rajendra
Oxidative C-C bond formation (Scholl reaction) with DDQ as an efficient and easily recyclable oxidant.
Organic letters, 2009, 11, 3474-3477
1504057 CIFC20 H19 N O4P 1 21/c 16.854; 7.879; 32.765
90; 90; 90
1769.4Xu, Silong; Zhou, Lili; Zeng, San; Ma, Renqin; Wang, Zhihong; He, Zhengjie
Phosphine-mediated olefination between aldehydes and allenes: an efficient synthesis of trisubstituted 1,3-dienes with high E-selectivity.
Organic letters, 2009, 11, 3498-3501
1504058 CIFC16 H17 N O6P -18.2434; 9.3954; 10.116
82.63; 84.66; 80.19
763.6Xu, Silong; Zhou, Lili; Zeng, San; Ma, Renqin; Wang, Zhihong; He, Zhengjie
Phosphine-mediated olefination between aldehydes and allenes: an efficient synthesis of trisubstituted 1,3-dienes with high E-selectivity.
Organic letters, 2009, 11, 3498-3501
1504059 CIFC16 H22 O7P 1 21/c 16.986; 24.324; 18.651
90; 90.932; 90
3168.9Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504060 CIFC16 H22 O7P 1 21/c 110.367; 10.635; 14.676
90; 100.819; 90
1589.3Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504061 CIFC19 H22 O4P 1 21/c 110.489; 13.758; 12.54
90; 123.65; 90
1506.4Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504062 CIFC12 H16 O3P 1 21/c 112.1; 7.3; 12.752
90; 111.89; 90
1045.2Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504063 CIFC21 H26 O6P 1 21/c 17.724; 27.076; 9.347
90; 100.51; 90
1922Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504064 CIFC25 H26 Br N O4P b c a17.103; 8.857; 29.744
90; 90; 90
4505.7Shintani, Ryo; Hayashi, Shin-ya; Murakami, Masataka; Takeda, Momotaro; Hayashi, Tamio
Stereoselective synthesis of spirooxindoles by palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with isatins.
Organic letters, 2009, 11, 3754-3756
1504065 CIFC16 H19 N O2P 1 21/c 17.1402; 12.5429; 15.2299
90; 101.104; 90
1338.44Li, Cheng; Li, Xinyu; Hong, Ran
Synthetic study on tetrapetalones: stereoselective cyclization of N-acyliminium ion to construct substituted 1-benzazepines.
Organic letters, 2009, 11, 4036-4039
1504066 CIFC16 H17 N O3P 21 21 217.6034; 12.7414; 13.9945
90; 90; 90
1355.76Li, Cheng; Li, Xinyu; Hong, Ran
Synthetic study on tetrapetalones: stereoselective cyclization of N-acyliminium ion to construct substituted 1-benzazepines.
Organic letters, 2009, 11, 4036-4039
1504067 CIFC24 H25 N OP 21 21 216.5177; 15.986; 18.6727
90; 90; 90
1945.55Concellón, José M; Tuya, Paula; del Solar, Virginia; García-Granda, Santiago; Díaz, M Rosario
Efficient and highly selective synthesis of enantiopure cis- or trans-3,4-disubstituted 1,2,3,4-tetrahydroisoquinolines.
Organic letters, 2009, 11, 3750-3753
1504068 CIFC24 H28 O6 S2P 1 21/c 110.3844; 11.1279; 19.5084
90; 98.041; 90
2232.2Tarselli, Michael A.; Zuccarello, J. Lucas; Lee, Stephen J.; Gagné, Michel R
Gold(I)-catalyzed cascade cyclization of allenyl epoxides.
Organic letters, 2009, 11, 3490-3492
1504069 CIFC34 H36 F6 Mn N4 O6 S2P 43 21 215.0588; 15.0588; 15.827
90; 90; 90
3589Wu, Mei; Wang, Bin; Wang, Shoufeng; Xia, Chungu; Sun, Wei
Asymmetric epoxidation of olefins with chiral bioinspired manganese complexes.
Organic letters, 2009, 11, 3622-3625
1504070 CIFC42 H40 F6 Mn N4 O6 S2P 21 21 2117.639; 16.204; 16.203
90; 90; 90
4631.2Wu, Mei; Wang, Bin; Wang, Shoufeng; Xia, Chungu; Sun, Wei
Asymmetric epoxidation of olefins with chiral bioinspired manganese complexes.
Organic letters, 2009, 11, 3622-3625
1504071 CIFC17 H22 Br N3 O5R 3 :H21.619; 21.619; 12.828
90; 90; 120
5192.3Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun
Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles.
Organic letters, 2009, 11, 3874-3877
1504072 CIFC23 H26 Cl N3 O5P -18.9418; 12.02; 12.756
115.51; 92.14; 107.65
1156.4Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun
Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles.
Organic letters, 2009, 11, 3874-3877
1504073 CIFC13 H11 N O SP 1 21 15.8503; 8.4929; 10.957
90; 95.88; 90
541.55Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun
Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles.
Organic letters, 2009, 11, 3874-3877
1504074 CIFC33 H24 OP 21 21 2110.4248; 11.0694; 20.658
90; 90; 90
2383.9Chen, Yifeng; Lu, Yuhua; Li, Guijie; Liu, Yuanhong
Gold-catalyzed cascade Friedel-Crafts/furan-alkyne cycloisomerizations for the highly efficient synthesis of arylated (Z)-enones or -enals.
Organic letters, 2009, 11, 3838-3841
1504075 CIFC16 H18 O2P 1 21/c 19.971; 8.96; 15.88
90; 103.924; 90
1377Zheng, Zhao-Jing; Shu, Xing-Zhong; Ji, Ke-Gong; Zhao, Shu-Chun; Liang, Yong-Min
Acid-catalyzed skeletal rearrangement of epoxy alkynes: a fast access to highly functionalized allenes.
Organic letters, 2009, 11, 3214-3217
1504076 CIFC15 H17 Cl O2P 1 21/c 19.4886; 8.7358; 16.598
90; 95.417; 90
1369.7Zheng, Zhao-Jing; Shu, Xing-Zhong; Ji, Ke-Gong; Zhao, Shu-Chun; Liang, Yong-Min
Acid-catalyzed skeletal rearrangement of epoxy alkynes: a fast access to highly functionalized allenes.
Organic letters, 2009, 11, 3214-3217
1504077 CIFC30 H34 B2 O4F d d 236.848; 45.584; 6.2397
90; 90; 90
10481Kimoto, Takakazu; Tanaka, Kenro; Sakai, Yoshimasa; Ohno, Akira; Yoza, Kenji; Kobayashi, Kenji
2,8- and 2,9-Diboryltetracenes as useful building blocks for extended pi-conjugated tetracenes.
Organic letters, 2009, 11, 3658-3661
1504078 CIFC26.52 H48.95 N8.26 O13.48 SC 1 2/c 121.0704; 8.8723; 20.4017
90; 121.08; 90
3266.5Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504079 CIFC26 H54 N8 O18 P2P -18.1169; 11.2001; 11.4236
108.885; 93.062; 107.523
923.8Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504080 CIFC32 H60 N8 O13 SP 1 21/c 110.753; 20.1934; 17.5334
90; 99.367; 90
3756.4Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504081 CIFC35.32 H62.76 N8 O14.77 PP 1 21/n 110.4079; 20.877; 20.852
90; 102.5; 90
4423.4Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504082 CIFC31 H56 N8 O14 P2P 1 21/c 121.554; 20.961; 17.568
90; 97.789; 90
7864Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504083 CIFC36 H52 N8 O8P b c a14.488; 18.236; 28.915
90; 90; 90
7639Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504084 CIFC17 H24 N2 O4C 1 2 123.342; 5.7712; 17.317
90; 130.887; 90
1763.6Duguet, Nicolas; Slawin, Alexandra M. Z.; Smith, Andrew D.
An asymmetric hetero-claisen approach to 3-alkyl-3-aryloxindoles.
Organic letters, 2009, 11, 3858-3861
1504085 CIFC15 H13 N O3P 1 21/c 111.11; 5.629; 20.2
90; 96.287; 90
1255.7Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504086 CIFC21 H19 N O4 SP -18.351; 9.897; 12.327
110.85; 90.686; 101.286
930Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504087 CIFC13 H15 N O2P 1 21/c 15.735; 15.439; 13.086
90; 110.233; 90
1087.2Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504088 CIFC18 H18 Cl3 N O3P n a 2110.096; 14.429; 13.147
90; 90; 90
1915.2Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504089 CIFC18 H19 N O3P 1 21/n 110.6641; 7.8382; 18.3358
90; 95.948; 90
1524.39Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504090 CIFC24 H20 O2F d d 219.0037; 35.6919; 10.5937
90; 90; 90
7185.5Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504091 CIFC21 H20 OP n a 2121.2315; 6.5111; 10.7839
90; 90; 90
1490.77Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504092 CIFC23 H20 O2P 1 21/n 116.7615; 10.1571; 20.7291
90; 108.722; 90
3342.36Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504093 CIFC60 H86 O8P -112.5; 12.906; 18.607
78.959; 78.684; 70.333
2746Kuno, Lev; Biali, Silvio E.
Restricted rotation of tert-butyl groups in sterically crowded methylene-functionalized calix[4]arenes.
Organic letters, 2009, 11, 3662-3665
1504094 CIFC28 H20 OP -19.6634; 13.954; 15.464
76.183; 88.614; 80.276
1995.5Meyer, S. Todd; Hergenrother, Paul J.
Small molecule ligands for bulged RNA secondary structures.
Organic letters, 2009, 11, 4052-4055
1504095 CIFC28 H20 OP 1 21/c 117.1785; 6.5035; 17.2798
90; 101.927; 90
1888.8Meyer, S. Todd; Hergenrother, Paul J.
Small molecule ligands for bulged RNA secondary structures.
Organic letters, 2009, 11, 4052-4055
1504096 CIFC23 H34 O4C 1 2 126.323; 6.1374; 13.3377
90; 96.461; 90
2141.1Chin, Yen-Jin; Wang, Shun-Yi; Loh, Teck-Peng
Synthesis of iriomoteolide-1a C13-C23 fragment via asymmetric conjugate addition and Julia-Kocienski coupling reaction.
Organic letters, 2009, 11, 3674-3676
1504097 CIFC20 H26 O3P -18.454; 10.416; 11.534
111.416; 94.438; 104.322
900.2Beauseigneur, Alice; Ericsson, Cecilia; Renaud, Philippe; Schenk, Kurt
B-Alkylcatecholborane-mediated tandem radical conjugated addition-aldol cyclization.
Organic letters, 2009, 11, 3778-3781
1504098 CIFC21 H28 O3P -18.5042; 10.5571; 11.489
110.098; 95.633; 104.645
917.6Beauseigneur, Alice; Ericsson, Cecilia; Renaud, Philippe; Schenk, Kurt
B-Alkylcatecholborane-mediated tandem radical conjugated addition-aldol cyclization.
Organic letters, 2009, 11, 3778-3781
1504099 CIFC14 H14 Cl N OP 1 21/n 19.601; 10.575; 12.022
90; 92.744; 90
1219.2Lu, Shen-Ci; Duan, Xiao-Yong; Shi, Zong-Jun; Li, Bing; Ren, Yu-Wei; Zhang, Wei; Zhang, Yong-Hui; Tu, Zhi-Feng
Photoinduced Intramolecular addition of 3-acyl-2-haloindoles to alkenes.
Organic letters, 2009, 11, 3902-3905
1504100 CIFC14 H14 Cl N OP 1 21/c 19.237; 15.927; 7.966
90; 93.364; 90
1169.92Lu, Shen-Ci; Duan, Xiao-Yong; Shi, Zong-Jun; Li, Bing; Ren, Yu-Wei; Zhang, Wei; Zhang, Yong-Hui; Tu, Zhi-Feng
Photoinduced Intramolecular addition of 3-acyl-2-haloindoles to alkenes.
Organic letters, 2009, 11, 3902-3905
1504101 CIFC12 H11 N3 O2P 1 21/n 17.5084; 8.3001; 17.5331
90; 92.508; 90
1091.6Shi, Baolu; Lewis, William; Campbell, Ian B.; Moody, Christopher J.
A concise route to pyridines from hydrazides by metal carbene N-H insertion, 1,2,4-triazine formation, and Diels-Alder reaction.
Organic letters, 2009, 11, 3686-3688
1504102 CIFC26 H20 N2P 21 21 2110.0514; 10.6807; 17.5467
90; 90; 90
1883.74Eisch, John J.; Manchanayakage, Renuka N.; Rheingold, Arnold L.
Attempted generation of the potentially aromatic 6,7-diphenyldibenzo[e,g][1,4]diazocine dianion leads with profound rearrangement to the isomeric n-(2-amino-1,2-diphenylethenyl)carbazole dianions.
Organic letters, 2009, 11, 4060-4063
1504103 CIFC26 H20 N2P -17.3565; 13.3596; 19.9232
92.014; 98.566; 99.128
1908.2Eisch, John J.; Manchanayakage, Renuka N.; Rheingold, Arnold L.
Attempted generation of the potentially aromatic 6,7-diphenyldibenzo[e,g][1,4]diazocine dianion leads with profound rearrangement to the isomeric n-(2-amino-1,2-diphenylethenyl)carbazole dianions.
Organic letters, 2009, 11, 4060-4063
1504104 CIFC27 H24 N2 O3P b c n33.2133; 7.9061; 17.9377
90; 90; 90
4710.2Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504105 CIFC25 H26 N2 O3P -19.0795; 11.1502; 11.7893
65.448; 88.094; 78.917
1063.91Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504106 CIFC27 H26 N2 O3P 1 21/n 110.824; 14.282; 16.681
90; 101.355; 90
2528.2Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504107 CIFC25 H28 N2 O3P b c a13.0902; 16.4023; 19.4869
90; 90; 90
4184Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504108 CIFC30 H48 N2 O13P 21 21 219.3504; 18.666; 20.153
90; 90; 90
3517.4Gao, Zheng-Xi; Wang, Meng; Wang, Shaozhong; Yao, Zhu-Jun
Efficient synthesis of 4-amido-N(5)-acetyl-4-deoxyneuraminic acid and its application to the C-4 modification of sialic acids.
Organic letters, 2009, 11, 3678-3681
1504109 CIFC18 H2 Br N4 O2P 1 21/c 17.816; 19.39; 12.728
90; 91.5; 90
1928.3Semakin, Artem N.; Sukhorukov, Alexey Yu; Lesiv, Alexey V.; Ioffe, Sema L.; Lyssenko, Konstantin A.; Nelyubina, Yulia V.; Tartakovsky, Vladimir A.
Unusual intramolecular cyclization of tris(beta-oximinoalkyl)amines. the first synthesis of 1,4,6,10-tetraazaadamantanes.
Organic letters, 2009, 11, 4072-4075
1504110 CIFC22 H50 N8 O16P 1 21 18.0368; 16.0616; 11.7596
90; 100.562; 90
1492.26Semakin, Artem N.; Sukhorukov, Alexey Yu; Lesiv, Alexey V.; Ioffe, Sema L.; Lyssenko, Konstantin A.; Nelyubina, Yulia V.; Tartakovsky, Vladimir A.
Unusual intramolecular cyclization of tris(beta-oximinoalkyl)amines. the first synthesis of 1,4,6,10-tetraazaadamantanes.
Organic letters, 2009, 11, 4072-4075
1504111 CIFC22 H20 SiP -19.318; 9.838; 10.808
77.76; 68.27; 70.39
862.6Ilies, Laurean; Tsuji, Hayato; Nakamura, Eiichi
Synthesis of benzo[b]siloles via KH-promoted cyclization of (2-alkynylphenyl)silanes.
Organic letters, 2009, 11, 3966-3968
1504112 CIFC73 H105.74 F24 N40 Na3.33 O56.53C 1 2/c 151.867; 16.796; 36.2025
90; 124.185; 90
26089.2Huang, Wei-Hao; Zavalij, Peter Y.; Isaacs, Lyle
Metal-ion-induced folding and dimerization of a glycoluril decamer in water.
Organic letters, 2009, 11, 3918-3921
1504113 CIFC120 H174.15 F9 N80 Na7 O81.07 S2P -123.465; 30.5747; 31.8174
108.231; 99.079; 110.589
19353.8Huang, Wei-Hao; Zavalij, Peter Y.; Isaacs, Lyle
Metal-ion-induced folding and dimerization of a glycoluril decamer in water.
Organic letters, 2009, 11, 3918-3921
1504114 CIFC24 H18 Cl2 O2P 1 21 16.797; 27.1487; 10.6266
90; 100.197; 90
1929.95Oswald, Claire L.; Peterson, Justine A.; Lam, Hon Wai
Enantioselective copper-catalyzed reductive Michael cyclizations.
Organic letters, 2009, 11, 4504-4507
1504115 CIFC29 H29 Cl2 N O5P 1 21/c 16.1649; 8.0908; 51.2892
90; 92.662; 90
2555.49Oswald, Claire L.; Peterson, Justine A.; Lam, Hon Wai
Enantioselective copper-catalyzed reductive Michael cyclizations.
Organic letters, 2009, 11, 4504-4507
1504116 CIFC14 H13 N O4 SP 1 21/n 19.2571; 13.4283; 11.0755
90; 94.92; 90
1371.69Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K.
Acyl-isothiocyanates as efficient thiocyanate transfer reagents.
Organic letters, 2009, 11, 3382-3385
1504117 CIFC20 H16 N2 O4 S2C 1 2/c 132.3486; 7.7362; 18.9463
90; 124.921; 90
3887.7Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K.
Acyl-isothiocyanates as efficient thiocyanate transfer reagents.
Organic letters, 2009, 11, 3382-3385
1504118 CIFC10 H9 N O2 SP b c a9.4658; 10.2821; 19.9354
90; 90; 90
1940.28Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K.
Acyl-isothiocyanates as efficient thiocyanate transfer reagents.
Organic letters, 2009, 11, 3382-3385
1504119 CIFC17 H15 I N2 O2P 1 21/n 17.8625; 10.7999; 18.3965
90; 90.968; 90
1561.9Kramer, Søren; Dooleweerdt, Karin; Lindhardt, Anders Thyboe; Rottländer, Mario; Skrydstrup, Troels
Highly regioselective Au(I)-catalyzed hydroamination of ynamides and propiolic acid derivatives with anilines.
Organic letters, 2009, 11, 4208-4211
1504120 CIFC27 H23 N O4 SP 1 21 112.7746; 5.8697; 16.037
90; 102.412; 90
1174.4Lu, Hai-Hua; Zhang, Fu-Gen; Meng, Xiang-Gao; Duan, Shu-Wen; Xiao, Wen-Jing
Enantioselective Michael reactions of beta, beta-disubstituted nitroalkenes: a new approach to beta(2,2)-amino acids with hetero-quaternary stereocenters.
Organic letters, 2009, 11, 3946-3949
1504121 CIFC23 H23 Br N O4 SP 1 21/c 110.96; 16.77; 12.38
90; 100.46; 90
2237.6Wei, Jun-Fa; Chen, Zhan-Guo; Lei, Wei; Zhang, Li-Hui; Wang, Ming-Zheng; Shi, Xian-Ying; Li, Run-Tao
Silicon powder: the first nonmetal elemental catalyst for aminobromination of olefins with TsNH(2) and NBS.
Organic letters, 2009, 11, 4216-4219
1504122 CIFC23 H21 Br N O4 SP -110.503; 11.062; 12.012
91.99; 112.83; 116.73
1111.1Wei, Jun-Fa; Chen, Zhan-Guo; Lei, Wei; Zhang, Li-Hui; Wang, Ming-Zheng; Shi, Xian-Ying; Li, Run-Tao
Silicon powder: the first nonmetal elemental catalyst for aminobromination of olefins with TsNH(2) and NBS.
Organic letters, 2009, 11, 4216-4219
1504123 CIFC21 H12 N2 OP n a 2115.884; 4.626; 19.4181
90; 90; 90
1426.83Haag, Benjamin; Peng, Zhihua; Knochel, Paul
Preparation of polyfunctional indazoles and heteroarylazo compounds using highly functionalized zinc reagents.
Organic letters, 2009, 11, 4270-4273
1504124 CIFC18 H20 O6P 1 21/c 19.117; 8.628; 19.717
90; 95.16; 90
1544.7Geng, Chang-An; Jiang, Zhi-Yong; Ma, Yun-Bao; Luo, Jie; Zhang, Xue-Mei; Wang, Hong-Ling; Shen, Yong; Zuo, Ai-Xue; Zhou, Jun; Chen, Ji-Jun
Swerilactones A and B, anti-HBV new lactones from a tradtional Chinese herb: Swertia mileensis as a treatment for viral hepatitis.
Organic letters, 2009, 11, 4120-4123
1504125 CIFC18 H21 O6P 1 c 17.4578; 15.834; 7.0431
90; 111.745; 90
772.5Geng, Chang-An; Jiang, Zhi-Yong; Ma, Yun-Bao; Luo, Jie; Zhang, Xue-Mei; Wang, Hong-Ling; Shen, Yong; Zuo, Ai-Xue; Zhou, Jun; Chen, Ji-Jun
Swerilactones A and B, anti-HBV new lactones from a tradtional Chinese herb: Swertia mileensis as a treatment for viral hepatitis.
Organic letters, 2009, 11, 4120-4123
1504126 CIFC24 H12C 1 2/c 119.932; 11.06; 15.993
90; 125.953; 90
2854Umeda, Rui; Hibi, Daijiro; Miki, Koji; Tobe, Yoshito
Tetradehydrodinaphtho[10]annulene: a hitherto unknown dehydroannulene and a viable precursor to stable zethrene derivatives.
Organic letters, 2009, 11, 4104-4106
1504127 CIFC15 H15 Cl O2P 21 21 215.2032; 12.4052; 20.7454
90; 90; 90
1339.05Marqués-López, Eugenia; Herrera, Raquel P.; Marks, Timo; Jacobs, Wiebke C.; Könning, Daniel; de Figueiredo, Renata M.; Christmann, Mathias
Crossed intramolecular Rauhut-Currier-type reactions via dienamine activation.
Organic letters, 2009, 11, 4116-4119
1504128 CIFC42 H52 N4 O3P 1 21 112.7151; 8.5294; 17.2463
90; 108.811; 90
1770.5Gan, Chew-Yan; Robinson, Ward T.; Etoh, Tadahiro; Hayashi, Masahiko; Komiyama, Kanki; Kam, Toh-Seok
Leucophyllidine, a cytotoxic bisindole alkaloid constituted from the union of an eburnan and a new vinylquinoline alkaloid.
Organic letters, 2009, 11, 3962-3965
1504129 CIFC20 H20 O7P -16.9331; 8.3871; 16.424
102.313; 91.417; 97.461
923.81Zheng, Suqing; Lu, Xiyan
Phosphine-catalyzed [4 + 3] annulation for the synthesis of highly functionalized bicyclo[3.2.2]nonadienes.
Organic letters, 2009, 11, 3978-3981
1504130 CIFC98 H104 Cl8 N4 O2P 1 21/c 114.7357; 17.0703; 17.6198
90; 105.354; 90
4273.94Stepień, Marcin; Szyszko, Bartosz; Latos-Grazyński, Lechosław
Steric control in the synthesis of p-benziporphyrins. Formation of a doubly N-confused benzihexaphyrin macrocycle.
Organic letters, 2009, 11, 3930-3933
1504131 CIFC12 H6 O6A b a 210.4174; 37.939; 10.277
90; 90; 90
4061.7Li, Yan; Lampkins, Andrew J.; Baker, Matthew B.; Sumpter, Bobby G.; Huang, Jingsong; Abboud, Khalil A.; Castellano, Ronald K.
Benzotrifuranone: synthesis, structure, and access to polycyclic heteroaromatics.
Organic letters, 2009, 11, 4314-4317
1504132 CIFC18 B2 F12 O4P 1 21/n 15.998; 14.15; 9.877
90; 92.99; 90
837Ono, Katsuhiko; Hashizume, Junko; Yamaguchi, Hiroyuki; Tomura, Masaaki; Nishida, Jun-ichi; Yamashita, Yoshiro
Synthesis, crystal structure, and electron-accepting property of the BF2 complex of a dihydroxydione with a perfluorotetracene skeleton.
Organic letters, 2009, 11, 4326-4329
1504133 CIFC12 H16 N2 O3 SP 1 21/n 16.2673; 25.0168; 8.7697
90; 105.982; 90
1321.84Pelletier, Sophie M.-C.; Ray, Peter C.; Dixon, Darren J.
Nitro-Mannich/lactamization cascades for the direct stereoselective synthesis of pyrrolidin-2-ones.
Organic letters, 2009, 11, 4512-4515
1504134 CIFC6 H7 Cl O3P 21 21 216.2776; 8.4084; 12.6034
90; 90; 90
665.27Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic access to versatile epoxyquinol synthons.
Organic letters, 2009, 11, 4290-4293
1504135 CIFC6 H7 Br O3P 21 21 216.4569; 8.5563; 12.5272
90; 90; 90
692.09Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic access to versatile epoxyquinol synthons.
Organic letters, 2009, 11, 4290-4293
1504136 CIFC6 H7 I O3P 21 21 216.8869; 8.8262; 12.2911
90; 90; 90
747.12Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic access to versatile epoxyquinol synthons.
Organic letters, 2009, 11, 4290-4293
1504137 CIFC25 H19 N O4P 21 21 216.2109; 15.5608; 21.4507
90; 90; 90
2073.1Nibbs, Antoinette E.; Baize, Amanda-Lauren; Herter, Rachel M.; Scheidt, Karl A.
Catalytic asymmetric alkylation of substituted isoflavanones.
Organic letters, 2009, 11, 4010-4013
1504138 CIFC27 H27 Br N2 O6 S SiP 1 21/n 115.3551; 21.005; 17.9066
90; 92.464; 90
5770.1Brawn, Ryan A.; Panek, James S.
Synthesis of enantioenriched homopropargylic sulfonamides by a three component reaction of aldehydes, sulfonamides, and chiral allenylsilanes.
Organic letters, 2009, 11, 4362-4365
1504139 CIFC20 H14 Br2P 1 21/c 19.4002; 12.978; 6.5114
90; 98.955; 90
784.7Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504140 CIFC20 H14 I2P 1 21/c 18.8964; 4.3883; 20.521
90; 91.043; 90
801Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504141 CIFC20 H14 Cl2P 1 21/c 19.0002; 12.78; 6.5335
90; 98.782; 90
742.7Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504142 CIFC20 H14 F2P 1 21/c 18.272; 12.739; 6.63
90; 100.662; 90
686.6Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504143 CIFC20 H14 Br2P 1 21/n 14.8281; 20.915; 7.4401
90; 90.051; 90
751.3Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504144 CIFC20 H14P b c a7.9296; 11.5575; 14.399
90; 90; 90
1319.6Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504145 CIFC40 H40P -110.432; 11.282; 13.32
102.375; 92.892; 106.548
1457.4Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504146 CIFC20 H14 Br2P 1 21/n 128.496; 4.0216; 29.455
90; 110.436; 90
3163.1Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504147 CIFC18 H19 N O5C 1 c 114.725; 16.2; 6.768
90; 91.991; 90
1613Barabé, Francis; Bétournay, Geneviève; Bellavance, Gabriel; Barriault, Louis
Gold-catalyzed synthesis of carbon-bridged medium-sized rings.
Organic letters, 2009, 11, 4236-4238
1504148 CIFC22 H18 Cl2 OP 1 21 110.5484; 8.7351; 10.6236
90; 114.794; 90
888.64Ji, Yining; Riera, Antoni; Verdaguer, Xavier
Asymmetric intermolecular Pauson-Khand reaction of symmetrically substituted alkynes.
Organic letters, 2009, 11, 4346-4349
1504149 CIFC14 H21 N5 O4 SeP -16.2068; 10.0735; 14.6424
105.53; 94.385; 97.243
869.2Goswami, Shyamaprosad; Hazra, Anita; Chakrabarty, Rinku; Fun, Hoong-Kun
Recognition of carboxylate anions and carboxylic acids by selenium-based new chromogenic fluorescent sensor: a remarkable fluorescence enhancement of hindered carboxylates.
Organic letters, 2009, 11, 4350-4353
1504150 CIFC16 H26 N2 O4R -3 :H28.99; 28.99; 10.1877
90; 90; 120
7414.9Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions.
Organic letters, 2009, 11, 4540-4543
1504151 CIFC21 H31 N2 O4P -18.834; 10.2781; 13.2981
90.009; 106.126; 98.122
1147.3Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions.
Organic letters, 2009, 11, 4540-4543
1504152 CIFC21 H38 N2 O7P -110.3811; 11.0624; 11.7553
109.649; 93.374; 115.456
1114.6Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions.
Organic letters, 2009, 11, 4540-4543
1504153 CIFC34 H25 Br N4P 1 21/c 19.5831; 13.0254; 23.2091
90; 96.634; 90
2877.6Yeagley, Andrew A.; Lowder, Melissa A.; Chruma, Jason J.
Tandem C-C bond-forming processes: interception of the pd-catalyzed decarboxylative allylation of allyl diphenylglycinate imines with activated olefins.
Organic letters, 2009, 11, 4022-4025
1504154 CIFC141 H88 F8P -114.2342; 16.3982; 23.0578
106.176; 91.373; 106.571
4922.9Thirion, Damien; Poriel, Cyril; Barrière, Frédéric; Métivier, Rémi; Jeannin, Olivier; Rault-Berthelot, Joëlle
Tuning the optical properties of aryl-substituted dispirofluorene-indenofluorene isomers through intramolecular excimer formation.
Organic letters, 2009, 11, 4794-4797
1504155 CIFC13 H8 N2 O2 S2P 1 21/n 17.4427; 9.3482; 18.2369
90; 95.639; 90
1262.71Murru, Siva; Ghosh, Harisadhan; Sahoo, Santosh K.; Patel, Bhisma K.
Intra- and intermolecular C-S bond formation using a single catalytic system: first direct access to arylthiobenzothiazoles.
Organic letters, 2009, 11, 4254-4257
1504156 CIFC28 H26 N2 O7 SP 1 21/c 111.33; 10.825; 21.832
90; 96.054; 90
2662.7Schuler, Marie; Duvvuru, Deepti; Retailleau, Pascal; Betzer, Jean-François; Marinetti, Angela
New access to trisubstituted 3-pyrrolines under phosphine catalysis.
Organic letters, 2009, 11, 4406-4409
1504157 CIFC33 H43 Br O5P 1 21/n 118.028; 8.953; 19.479
90; 98.94; 90
3105.8Couladouros, Elias A.; Dakanali, Marianna; Demadis, Konstantinos D.; Vidali, Veroniki P.
A short biomimetic approach to the fully functionalized bicyclic framework of type A acylphloroglucinols.
Organic letters, 2009, 11, 4430-4433
1504158 CIFC34 H56 N12 O17P 1 21/m 110.4708; 19.8848; 10.7309
90; 116.395; 90
2001.36Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504159 CIFC46 H59 I2 N14 O11.5P 1 21/c 115.4095; 13.0685; 25.1488
90; 94.613; 90
5048.04Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504160 CIFC46 H60 I2 N14 O13P 1 21/n 114.5007; 13.3573; 27.3613
90; 93.266; 90
5291Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504161 CIFC41 H58 I N13 O14P 1 21/n 113.0994; 14.8054; 24.1661
90; 92.029; 90
4683.88Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504162 CIFC24 H38 N12 O10P 1 21/c 19.4511; 13.8492; 21.2892
90; 99.131; 90
2751.24Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504163 CIFC18 H15 Br O2P 21 21 215.7231; 12.9531; 20.0245
90; 90; 90
1484.45Gregg, Timothy M.; Farrugia, Mark K.; Frost, John R.
Rhodium-mediated enantioselective cyclopropanation of allenes.
Organic letters, 2009, 11, 4434-4436
1504164 CIFC45 H40 N4 O5.5P 1 21/c 113.2356; 12.1782; 26.593
90; 102.202; 90
4189.6Zhou, Ying; Wang, Fang; Kim, Youngmee; Kim, Sung-Jin; Yoon, Juyoung
Cu2±selective ratiometric and "off-on" sensor based on the rhodamine derivative bearing pyrene group.
Organic letters, 2009, 11, 4442-4445
1504165 CIFC24 N2 O2P 1 21/n 19.668; 9.511; 19.728
90; 90.66; 90
1813.9Zhou, Ying; Wang, Fang; Kim, Youngmee; Kim, Sung-Jin; Yoon, Juyoung
Cu2±selective ratiometric and "off-on" sensor based on the rhodamine derivative bearing pyrene group.
Organic letters, 2009, 11, 4442-4445
1504166 CIFC392 H360 F48 N8 O48 P8P 1 21/n 116; 24.7; 24.3
90; 103.4; 90
9342Cao, Jing; Lu, Hai-Yan; You, Xiao-Jun; Zheng, Qi-Yu; Chen, Chuan-Feng
Complexation of a pentiptycene-based tweezer-like receptor with paraquat derivatives: ion-controlled binding and release of the guests.
Organic letters, 2009, 11, 4446-4449
1504167 CIFC20 H14 N4 SP 1 21/c 18.9001; 11.3943; 14.9742
90; 91.902; 90
1517.7Balaji, Ganapathy; Shim, Wong Low; Parameswaran, Manoj; Valiyaveettil, Suresh
Thiadiazole fused indolo[2,3-a]carbazole based oligomers and polymer.
Organic letters, 2009, 11, 4450-4453
1504168 CIFC39 H40 O6 S4P -111.784; 15.222; 20.955
100.82; 102.15; 90.23
3605.6Kundrat, Ondrej; Dvorakova, Hana; Cisarova, Ivana; Pojarova, Michaela; Lhotak, Pavel
Unusual intramolecular bridging reaction in thiacalix[4]arene series.
Organic letters, 2009, 11, 4188-4191
1504169 CIFC25 H27 N3 O3P 1 21/c 19.7384; 12.008; 19.3474
90; 94.943; 90
2254Jiang, Gaoxi; Chen, Jian; Huang, Jie-Sheng; Che, Chi-Ming
Highly efficient oxidation of amines to imines by singlet oxygen and its application in Ugi-type reactions.
Organic letters, 2009, 11, 4568-4571
1504170 CIFC16 H22 O SP 1 21/n 113.777; 6.552; 16.81
90; 108.452; 90
1439.4Liu, Taoping; Zhao, Xiaoming; Lu, Long; Cohen, Theodore
Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent.
Organic letters, 2009, 11, 4576-4579
1504171 CIFC18 H24 O SP b c a9.2519; 16.7091; 20.816
90; 90; 90
3218Liu, Taoping; Zhao, Xiaoming; Lu, Long; Cohen, Theodore
Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent.
Organic letters, 2009, 11, 4576-4579
1504172 CIFC13 H20 N2 SiP n a 2110.6; 14.995; 8.7526
90; 90; 90
1391.2Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng
Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes.
Organic letters, 2009, 11, 4458-4461
1504173 CIFC27 H30 N4 O2 SiP -112.696; 14.502; 15.33
74.95; 71.74; 79.67
2573.6Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng
Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes.
Organic letters, 2009, 11, 4458-4461
1504174 CIFC31 H29 Br3 N6 O4P -110.299; 12.584; 12.776
82.36; 88.14; 72.95
1568.9Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng
Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes.
Organic letters, 2009, 11, 4458-4461
1504175 CIFC84 H27 Cl2 N O SiP 1 21/n 119.1274; 13.9545; 19.5256
90; 108.304; 90
4947.96Matsuo, Keiko; Matsuo, Yutaka; Iwashita, Akihiko; Nakamura, Eiichi
Synthesis of imino[60]fullerenes using nitriles and trimethylsilylmethyl triflate.
Organic letters, 2009, 11, 4192-4194
1504176 CIFC22 H26 N2 O2P 1 21/c 18.816; 13.762; 31.213
90; 94.584; 90
3774.83Grant, Christopher D.; Krische, Michael J.
Protecting-group-free synthesis of 3-tert-prenylated oxindoles: contiguous all-carbon quaternary centers via tertiary neopentyl substitution.
Organic letters, 2009, 11, 4485-4487
1504177 CIFC22 H19 N O5P 21 21 215.7776; 16.337; 20.021
90; 90; 90
1889.8Li, Hongyan; Hsung, Richard P.
Highly substituted 2-amido-furans from Rh(II)-catalyzed cyclopropenations of ynamides.
Organic letters, 2009, 11, 4462-4465
1504178 CIFC79 H95 F12 N7 O16 P2P -114.3156; 15.2385; 21.0682
86.801; 82.424; 66.377
4174.1Yen, Ming-Liang; Chen, Nai-Chia; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
A molecular cage that selectively complexes three different guests in solution.
Organic letters, 2009, 11, 4604-4607
1504179 CIFC28 H27 Cl Cu0.5 N9 O2P -19.6706; 11.7736; 12.4516
80.677; 81.72; 81.309
1372.5Ozçubukçu, Salih; Ozkal, Erhan; Jimeno, Ciril; Pericàs, Miquel A
A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure.
Organic letters, 2009, 11, 4680-4683
1504180 CIFC20 H20 O8P 1 21 16.547; 10.892; 12.418
90; 103.542; 90
860.9Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun
Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis.
Organic letters, 2009, 11, 4838-4841
1504181 CIFC20 H22 O9P -18.6844; 14.094; 17
73.293; 87.688; 72.958
1903.2Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun
Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis.
Organic letters, 2009, 11, 4838-4841
1504182 CIFC24 H36 Cl N2 O7P 21 21 219.268; 13.934; 19.073
90; 90; 90
2463.1Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong
Melohenines A and B, two unprecedented alkaloids from Melodinus henryi
Organic Letters, 2009, 11, 4834-4837
1504183 CIFC19 H24 N2 O3P 21 21 217.9717; 12.2181; 17.265
90; 90; 90
1681.6Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong
Melohenines A and B, two unprecedented alkaloids from Melodinus henryi
Organic Letters, 2009, 11, 4834-4837
1504184 CIFC15 H11 N3 O2P 1 21/c 119.1116; 4.165; 16.2443
90; 111.391; 90
1203.97Board, Johnathan; Wang, Jian-Xin; Crew, Andrew P.; Jin, Meizhong; Foreman, Kenneth; Mulvihill, Mark J.; Snieckus, Victor
Synthesis of substituted imidazo[1,5-a]pyrazines via mono-, di-, and directed remote metalation strategies.
Organic letters, 2009, 11, 5118-5121
1504185 CIFC16 H18 O4C 1 2 118.1933; 7.711; 12.4502
90; 129.39; 90
1349.87Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504186 CIFC16 H18 O5P 21 21 217.8053; 9.4883; 18.9039
90; 90; 90
1400Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504187 CIFC17 H20 O5C 1 2 118.1525; 7.6684; 12.0226
90; 101.178; 90
1641.81Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504188 CIFC16 H18 O5P 21 21 219.597; 9.9935; 14.1873
90; 90; 90
1360.67Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504189 CIFC19 H24 O4P 21 21 217.7249; 9.6338; 22.5067
90; 90; 90
1674.95Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504190 CIFC19 H22 O4P 21 21 217.7635; 9.7864; 21.0195
90; 90; 90
1596.99Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504191 CIFC17 H20 O6P 21 21 216.1894; 8.9465; 28.8255
90; 90; 90
1596.17Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504192 CIFC16 H18 O6P 21 21 218.2864; 10.0771; 17.1744
90; 90; 90
1434.11Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504193 CIFC17 H20 O6P 21 21 2111.0321; 11.6526; 11.9913
90; 90; 90
1541.51Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504194 CIFC15 H22 O3P -18.8984; 9.621; 16.7771
89.599; 85.959; 85.973
1429.2Hampel, Thomas; Brückner, Reinhard
A novel cis-selective cyclohexanone annulation as the key step of a total synthesis of the sesquiterpene isoacanthodoral.
Organic letters, 2009, 11, 4842-4845
1504195 CIFC18 H13 F3 O9 SP 1 21/c 118.964; 13.633; 29.823
90; 92.316; 90
7704Cui, Yi; Jiang, Hao; Li, Zhengtao; Wu, Na; Yang, Zhen; Quan, Junmin
Unexpected regioselectivity in the synthesis of pyranonaphthoquinone via the Diels-Alder reaction.
Organic letters, 2009, 11, 4628-4631
1504196 CIFC9 H12 O3 SP 1 21 17.6288; 5.445; 11.5547
90; 91.844; 90
479.72Majer, Jakub; Kwiatkowski, Piotr; Jurczak, Janusz
Highly enantioselective Friedel-Crafts reaction of thiophenes with glyoxylates: formal synthesis of duloxetine.
Organic letters, 2009, 11, 4636-4639
1504197 CIFC18 H27 N O6P 21 21 219.355; 11.918; 17.31
90; 90; 90
1929.9Gross, Ulrike; Nieger, Martin; Bräse, Stefan
Stereoselective synthesis of the epicoccin core.
Organic letters, 2009, 11, 4740-4742
1504198 CIFC22 H27 N O7P 1 21 17.715; 15.086; 9.295
90; 96.54; 90
1074.8Balthaser, Bradley R.; McDonald, Frank E.
Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins.
Organic letters, 2009, 11, 4850-4853
1504199 CIFC22 H27 N O7P 1 21 113.2879; 9.2997; 17.411
90; 100.194; 90
2117.57Balthaser, Bradley R.; McDonald, Frank E.
Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins.
Organic letters, 2009, 11, 4850-4853
1504200 CIFC22 H35 N O11P 21 21 218.1737; 10.9997; 29.222
90; 90; 90
2627.3Balthaser, Bradley R.; McDonald, Frank E.
Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins.
Organic letters, 2009, 11, 4850-4853
1504201 CIFC28.5 H31 ClC 1 2/c 125.9973; 12.3802; 13.8796
90; 93.724; 90
4457.74Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504202 CIFC30 H34P -111.075; 14.841; 15.693
118.089; 91.405; 92.655
2270Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504203 CIFC30 H34 O2P 1 21/c 110.6975; 10.0435; 10.8065
90; 101.43; 90
1138.03Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504204 CIFC30 H34 O2P 1 21/c 114.0575; 10.3006; 8.0732
90; 99.533; 90
1152.86Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504205 CIFC30 H34 O2.96R -3 :H21.0561; 21.0561; 14.3941
90; 90; 120
5526.77Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504206 CIFC32 H38 O4P 1 21/n 19.6612; 6.9042; 19.3657
90; 94.574; 90
1287.63Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504207 CIFC48 H54P 1 21/c 121.8162; 9.4664; 8.9027
90; 90.648; 90
1838.5Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504208 CIFC66 H86P 1 21/n 111.9837; 36.2583; 18.6597
90; 95.013; 90
8076.8Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504209 CIFC40 H50 Cl4 O4P 1 21/c 112.5705; 9.6243; 15.996
90; 106.347; 90
1857Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504210 CIFC23 H22 Cl N O3P 1 21 110.185; 8.74; 12.189
90; 112.29; 90
1003.9Han, Bo; Xiao, You-Cai; He, Zhao-Quan; Chen, Ying-Chun
Asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins via dienamine catalysis.
Organic letters, 2009, 11, 4660-4663
1504211 CIFC12 H9 N O4P 1 21/n 16.0584; 19.717; 8.9513
90; 98.257; 90
1058.2Huo, Fang-Jun; Sun, Yuan-Qiang; Su, Jing; Chao, Jian-Bin; Zhi, Hai-Juan; Yin, Cai-Xia
Colorimetric detection of thiols using a chromene molecule
Organic letters, 2009, 11, 4918-4921
1504212 CIFC17 H15 B F4 O3P 1 21/n 112.7974; 7.6261; 17.351
90; 105.01; 90
1635.6Hu, Zhi-Long; Qian, Wen-Jian; Wang, Sheng; Wang, Shaozhong; Yao, Zhu-Jun
Transformation of reactive isochromenylium intermediates to stable salts and their cascade reactions with olefins.
Organic letters, 2009, 11, 4676-4679
1504213 CIFC21 H28 O10P 21 21 2110.0245; 12.5364; 17.6378
90; 90; 90
2216.6Afarinkia, Kamyar; Abdullahi, Mohamed Haji; Scowen, Ian J.
A new, general method for the synthesis of carbasugar-sugar pseudodisaccharides.
Organic letters, 2009, 11, 5182-5184
1504214 CIFC25 H40 O5 SiP 21 21 216.5381; 13.0869; 28.301
90; 90; 90
2421.5Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504215 CIFC27 H40 O7 SiC 1 2 127.8634; 7.012; 18.3625
90; 129.332; 90
2774.98Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504216 CIFC21 H24 O6P 1 21/n 17.1446; 10.9191; 23.7565
90; 91.941; 90
1852.24Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504217 CIFC21 H27 O7C 1 2 130.4299; 7.0493; 19.6268
90; 111.309; 90
3922.31Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504218 CIFC26 H21 O3P 18.4452; 10.6647; 11.566
82.23; 89.149; 77.425
1007.26Yoshida, Masahiro; Higuchi, Mariko; Shishido, Kozo
Stereoselective construction of substituted chromans by palladium-catalyzed cyclization of propargylic carbonates with 2-(2-hydroxyphenyl)acetates.
Organic letters, 2009, 11, 4752-4755
1504219 CIFC26 H33 N O3 SiP 17.718; 11.898; 14.296
96.932; 103.456; 108.338
1184.9Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar
Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process.
Organic letters, 2009, 11, 5230-5233
1504220 CIFC18 H21 N O4P 1 21/n 110.762; 12.294; 11.66
90; 106.56; 90
1478.7Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar
Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process.
Organic letters, 2009, 11, 5230-5233
1504221 CIFC29 H22 O2C 1 2/c 125.5017; 10.0101; 18.5411
90; 118.749; 90
4149.6Zhang, Xiaoxiang; Teo, Wan Teng; Chan, Philip Wai Hong
Ytterbium(III) triflate catalyzed tandem Friedel-Crafts alkylation/hydroarylation of propargylic alcohols with phenols as an expedient route to indenols.
Organic letters, 2009, 11, 4990-4993
1504222 CIFC20 H24 O2P 1 21/n 114.0468; 6.6546; 18.8942
90; 110.607; 90
1653.15Falck, J. R.; Bandyopadhyay, Anish; Puli, Narender; Kundu, Abhijit; Reddy, L. Manmohan; Barma, Deb K.; He, Anyu; Zhang, Hongming; Kashinath, Dhurke; Baati, Rachid
Cascade synthesis of (E)-2-alkylidenecyclobutanols.
Organic letters, 2009, 11, 4764-4766
1504223 CIFC20 H28 N2 O5 SP 1 21 111.9221; 10.8903; 16.4113
90; 105.351; 90
2054.74Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504224 CIFC15 H19 N O4 SP 21 21 2122.7128; 8.0293; 8.0067
90; 90; 90
1460.16Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504225 CIFC21 H23 N O4 SP 1 21 17.8477; 11.5372; 10.5434
90; 108.089; 90
907.42Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504226 CIFC16 H21 N O4 SP 21 21 212.1704; 17.3626; 7.5061
90; 90; 90
1586.11Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504227 CIFC18 H26 O2 SiP 1 21 15.9876; 7.3491; 19.9858
90; 97.689; 90
871.54Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504228 CIFC23 H29 N O4 SP 21 21 218.0984; 13.6158; 19.1081
90; 90; 90
2106.98Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504229 CIFC23 H27 N O4 SP 41 21 210.834; 10.834; 36.399
90; 90; 90
4272.35Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504230 CIFC21 H23 N O4 SP 21 21 217.76; 8.8993; 27.238
90; 90; 90
1881.02Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504231 CIFC26 H37 Cl N2 O4 SP 21 21 217.144; 11.902; 30.0352
90; 90; 90
2553.83Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504232 CIFC26 H31 Cl N2 O4 SP 21 21 217.1052; 11.8008; 28.9702
90; 90; 90
2429.07Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504233 CIFC25 H32 N O4 SP 1 21 110.3654; 10.9898; 10.6563
90; 104.714; 90
1174.09Webster, Robert; Lautens, Mark
Conformational effects in diastereoselective aryne Diels-Alder reactions: synthesis of benzo-fused [2.2.1] heterobicycles.
Organic letters, 2009, 11, 4688-4691
1504234 CIFC18 H26 O3P 1 21 16.7635; 13.1016; 9.4936
90; 99.898; 90
828.7Tseng, Yen-Ju; Wen, Zhi-Hong; Dai, Chang-Feng; Chiang, Michael Y.; Sheu, Jyh-Horng
Nanolobatolide, a new C18 metabolite from the Formosan soft coral Sinularia nanolobata.
Organic letters, 2009, 11, 5030-5032
1504235 CIFC24 H20 O2P n a 2110.3835; 18.167; 9.6747
90; 90; 90
1825Onodera, Gen; Kato, Minoru; Kawano, Ryo; Kometani, Yuri; Takeuchi, Ryo
Highly regio- and stereoselective addition of 1,3-diketones to internal alkynes catalyzed by cationic iridium complex.
Organic letters, 2009, 11, 5038-5041
1504236 CIFC15 H17 N O4P b c a9.03; 11.494; 26.562
90; 90; 90
2757Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko
Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals.
Organic letters, 2009, 11, 4902-4905
1504237 CIFC16 H19 N O4P b c a9.4786; 10.8076; 28.163
90; 90; 90
2885Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko
Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals.
Organic letters, 2009, 11, 4902-4905
1504238 CIFC14 H11 N O3P -17.7; 8.873; 16.958
99.1; 101.15; 92.16
1119.6Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko
Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals.
Organic letters, 2009, 11, 4902-4905
1504239 CIFC13 H13 N O3P 1 21/a 17.578; 17.794; 8.169
90; 87.67; 90
1100.6Kise, Naoki; Isemoto, Shinsaku; Sakurai, Toshihiko
Electroreductive coupling of phthalimides with alpha,beta-unsaturated esters: unusual rearrangement of resulting silyl ketene acetals.
Organic letters, 2009, 11, 4902-4905
1504240 CIFC38.76 H26.76 Cl2.28 N2 O4P 1 21/n 114.1491; 15.475; 14.3939
90; 90.06; 90
3151.6Maugel, Nathan; Snider, Barry B.
Efficient synthesis of the tetracyclic aminoquinone moiety of marmycin A.
Organic letters, 2009, 11, 4926-4929
1504241 CIFC23 H28 O3 SP 1 21 111.0848; 8.9222; 11.2461
90; 116.209; 90
997.9Hernández-Torres, Gloria; Urbano, Antonio; Carreño, M Carmen; Colobert, Françoise
Stereocontrolled generation of the (2R) chroman core of vitamin E: total synthesis of (2R,4'RS,8'RS)-alpha-tocopherol.
Organic letters, 2009, 11, 4930-4933
1504242 CIFC20 H17 Cl2 N OP 21 21 2112.5109; 15.341; 17.9478
90; 90; 90
3444.72Oinen, Mark Emil; Yu, Robert T.; Rovis, Tomislav
Excess substrate is a spectator ligand in a rhodium-catalyzed asymmetric [2 + 2 + 2] cycloaddition of alkenyl isocyanates with tolanes.
Organic letters, 2009, 11, 4934-4937
1504243 CIFC35 H27 Br Cl3 N O6P 1 21 115.8; 5.833; 18.339
90; 99.491; 90
1667Yu, Jie; He, Long; Chen, Xiao-Hua; Song, Jin; Chen, Wei-Jie; Gong, Liu-Zhu
Highly enantioselective catalytic 1,3-dipolar cycloaddition involving 2,3-allenoate dipolarophiles.
Organic letters, 2009, 11, 4946-4949
1504244 CIFC23 H21 N O4 S2P 21 21 216.0566; 11.2097; 30.664
90; 90; 90
2081.9Moreno-Clavijo, Elena; Carmona, Ana T.; Reissig, Hans-Ulrich; Moreno-Vargas, Antonio J; Alvarez, Eleuterio; Robina, Inmaculada
Allenyl sulfones and allenyl sulfides in the synthesis of 3-pyrrolines. A novel nucleophilic [3 + 2] cycloaddition on allenyl sulfones giving rearranged cycloadducts.
Organic letters, 2009, 11, 4778-4781
1504245 CIFC24 H23 N O5 S2P 21 21 215.9508; 11.729; 31.384
90; 90; 90
2190.5Moreno-Clavijo, Elena; Carmona, Ana T.; Reissig, Hans-Ulrich; Moreno-Vargas, Antonio J; Alvarez, Eleuterio; Robina, Inmaculada
Allenyl sulfones and allenyl sulfides in the synthesis of 3-pyrrolines. A novel nucleophilic [3 + 2] cycloaddition on allenyl sulfones giving rearranged cycloadducts.
Organic letters, 2009, 11, 4778-4781

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