Crystallography Open Database

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1515942 CIFC20.5 H21 Cl N2 O2P 1 21/c 111.233; 22.492; 7.1548
90; 99.452; 90
1783.1Min, Chang; Sanchawala, Abbas; Seidel, Daniel
Dual C-H Functionalization of N-Aryl Amines: Synthesis of Polycyclic Amines via an Oxidative Povarov Approach.
Organic letters, 2014, 16, 2756-2759
1515947 CIFC28 H37 N O5 SiP 21 21 215.368; 55.574; 6.2795
90; 90; 90
5363.1Trost, Barry M.; Ehmke, Veronika
An approach for rapid increase in molecular complexity: atom economic routes to fused polycyclic ring systems.
Organic letters, 2014, 16, 2708-2711
1515976 CIFC21 H32 O4P 1 21 16.0539; 11.5542; 13.5149
90; 102.108; 90
924.31Kumar, Chebolu Naga Sesha Sai Pavan; Chein, Rong-Jie
Synthesis of labdane diterpenes galanal a and B from (+)-sclareolide.
Organic letters, 2014, 16, 2990-2992
1515977 CIFC18 H23 N O5P 21 21 218.9976; 10.8156; 16.5526
90; 90; 90
1610.81Jhuo, Dai-Huei; Hong, Bor-Cherng; Chang, Chun-Wei; Lee, Gene-Hsiang
One-pot organocatalytic enantioselective Michael-Michael-aldol-Henry reaction cascade. A facile entry to the steroid system with six contiguous stereogenic centers.
Organic letters, 2014, 16, 2724-2727
1515978 CIFC18 H22 Br N O5P 21 21 218.9352; 29.3697; 6.2956
90; 90; 90
3501.1Jhuo, Dai-Huei; Hong, Bor-Cherng; Chang, Chun-Wei; Lee, Gene-Hsiang
One-pot organocatalytic enantioselective Michael-Michael-aldol-Henry reaction cascade. A facile entry to the steroid system with six contiguous stereogenic centers.
Organic letters, 2014, 16, 2724-2727
1515979 CIFC14 H19 N O4P 21 21 217.3853; 10.1226; 17.8638
90; 90; 90
1335.47Jhuo, Dai-Huei; Hong, Bor-Cherng; Chang, Chun-Wei; Lee, Gene-Hsiang
One-pot organocatalytic enantioselective Michael-Michael-aldol-Henry reaction cascade. A facile entry to the steroid system with six contiguous stereogenic centers.
Organic letters, 2014, 16, 2724-2727
1515980 CIFC36 H44 N4 O4P c a 2125.739; 9.667; 12.857
90; 90; 90
3199Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515981 CIFC44 H42 N2 O8 S2P -112.114; 12.234; 14.573
107.079; 98.454; 105.459
1929.4Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515982 CIFC44 H45 N3 O6 S2P 1 21/c 113.658; 11.024; 26.112
90; 100.241; 90
3869Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515983 CIFC36 H44 N4 O4P b c a12.802; 19.593; 25.555
90; 90; 90
6410Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515984 CIFC40 H46 N2 O8 S2P b c a29.124; 8.811; 29.171
90; 90; 90
7486Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515985 CIFC43 H40 N2 O8 S2P 1 21/c 113.109; 14.562; 19.787
90; 98.818; 90
3733Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515986 CIFC48 H52 N4 O8 S2P 1 21/c 19.393; 29.532; 15.825
90; 99.223; 90
4333Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515987 CIFC44 H49 N2 O7 S2P -110.515; 13.39; 15.724
84.427; 72.768; 67.283
1950.1Dethe, Dattatraya H.; Erande, Rohan D.; Dherange, Balu D.
Remarkable switch of regioselectivity in diels-alder reaction: divergent total synthesis of borreverine, caulindoles, and flinderoles.
Organic letters, 2014, 16, 2764-2767
1515988 CIFC36 H36 N4 O4P b c a10.915; 10.002; 27.209
90; 90; 90
2970.5Culf, Adrian S.; Cuperlović-Culf, Miroslava; Léger, Daniel A; Decken, Andreas
Small Head-to-Tail Macrocyclic α-Peptoids.
Organic letters, 2014, 16, 2780-2783
1515989 CIFC36 H36 N4 O4P 1 21/c 117.232; 5.508; 17.915
90; 114.836; 90
1543.1Culf, Adrian S.; Cuperlović-Culf, Miroslava; Léger, Daniel A; Decken, Andreas
Small Head-to-Tail Macrocyclic α-Peptoids.
Organic letters, 2014, 16, 2780-2783
1515990 CIFC27 H27 N3 O3P c a 2117.384; 9.096; 28.177
90; 90; 90
4455Culf, Adrian S.; Cuperlović-Culf, Miroslava; Léger, Daniel A; Decken, Andreas
Small Head-to-Tail Macrocyclic α-Peptoids.
Organic letters, 2014, 16, 2780-2783
1515991 CIFC45.5 H45.5 Cl1.5 N5 O5C 1 2/c 124.448; 13.284; 27.047
90; 102.463; 90
8577Culf, Adrian S.; Cuperlović-Culf, Miroslava; Léger, Daniel A; Decken, Andreas
Small Head-to-Tail Macrocyclic α-Peptoids.
Organic letters, 2014, 16, 2780-2783
1515992 CIFC46 H52 N4 O18P 6419.5118; 19.5118; 12.0531
90; 90; 120
3973.97Zhang, Juanli; Qian, Zhengyi; Wu, Xingkang; Ding, Yanjiao; Li, Jianfang; Lu, Chunhua; Shen, Yuemao
Juanlimycins A and B, Ansamycin Macrodilactams from Streptomyces sp.
Organic letters, 2014, 16, 2752-2755
1515994 CIFC17 H16 N2 O3 S2P 1 21/n 110.7362; 14.1883; 12.3716
90; 108.855; 90
1783.42Li, Yiming; Pu, Jiahua; Jiang, Xuefeng
A highly efficient cu-catalyzed s-transfer reaction: from amine to sulfide.
Organic letters, 2014, 16, 2692-2695
1516025 CIFC63 H54 B2 Cl3 F4 N6P -112.421; 14.0537; 17.9628
66.48; 79.82; 80.77
2815.8Yokoi, Hiroki; Hiroto, Satoru; Shinokubo, Hiroshi
Synthesis of Diazo-Bridged BODIPY Dimer and Tetramer by Oxidative Coupling of β-Amino-Substituted BODIPYs.
Organic letters, 2014, 16, 3004-3007
1516043 CIFC53 H64.5 F12 N5.5 O10 P2P -110.9871; 15.0321; 19.4495
67.41; 87.04; 85.923
2957.3Xing, Hao; Wei, Peifa; Yan, Xuzhou
Supramolecular Side-Chain Poly[2]pseudorotaxanes Formed by Orthogonal Coordination-Driven Self-Assembly and Crown-Ether-Based Host-Guest Interactions.
Organic letters, 2014, 16, 2850-2853
1516044 CIFC117 H122 N4 O2 ZnP -114.274; 16.988; 21.032
67.91; 80.65; 86.6
4662.8Ota, Kensuke; Tanaka, Takayuki; Osuka, Atsuhiro
meso-β Dibenzo[a,g]corannulene-Fused Porphyrins.
Organic letters, 2014, 16, 2974-2977
1516045 CIFC96.89 H88.31 N4 O1.72 ZnP -19.353; 21.838; 38.554
103.231; 90.09; 102.288
7480Ota, Kensuke; Tanaka, Takayuki; Osuka, Atsuhiro
meso-β Dibenzo[a,g]corannulene-Fused Porphyrins.
Organic letters, 2014, 16, 2974-2977
1516046 CIFC96 H98 N4 O2 ZnP -19.7687; 15.6035; 26.497
75.421; 83.382; 87.1181
3881.8Ota, Kensuke; Tanaka, Takayuki; Osuka, Atsuhiro
meso-β Dibenzo[a,g]corannulene-Fused Porphyrins.
Organic letters, 2014, 16, 2974-2977
1516047 CIFC23 H18 O2P -19.661; 9.9907; 10.7602
63.28; 80.45; 70.81
875.9Chagarovsky, Alexey O.; Budynina, Ekaterina M.; Ivanova, Olga A.; Villemson, Elena V.; Rybakov, Victor B.; Trushkov, Igor V.; Melnikov, Mikhail Ya
Reaction of Corey Ylide with α,β-Unsaturated Ketones: Tuning of Chemoselectivity toward Dihydrofuran Synthesis.
Organic letters, 2014, 16, 2830-2833
1516048 CIFC23 H23 N O3P 1 21/c 110.0605; 10.1253; 19.2983
90; 91.597; 90
1965.1Chagarovsky, Alexey O.; Budynina, Ekaterina M.; Ivanova, Olga A.; Villemson, Elena V.; Rybakov, Victor B.; Trushkov, Igor V.; Melnikov, Mikhail Ya
Reaction of Corey Ylide with α,β-Unsaturated Ketones: Tuning of Chemoselectivity toward Dihydrofuran Synthesis.
Organic letters, 2014, 16, 2830-2833
1516049 CIFC21 H23 F N2 OP 1 21/c 19.073; 11.096; 19.557
90; 94.205; 90
1963.6Thirupathi, Nuligonda; Hari Babu, Madala; Dwivedi, Vikas; Kant, Ruchir; Sridhar Reddy, Maddi
Palladium-Catalyzed Tandem Intramolecular Oxy/Amino-Palladation/Isocyanide Insertion: Synthesis of α-Benzofuranyl/Indolylacetamides.
Organic letters, 2014, 16, 2908-2911
1516050 CIFC26 H36 N2 O2P 21 21 2110.5434; 11.509; 19.6411
90; 90; 90
2383.3Seo, Min-Seob; Lee, Ansoo; Kim, Hyunwoo
2,2'-dihydroxybenzil: a stereodynamic probe for primary amines controlled by steric strain.
Organic letters, 2014, 16, 2950-2953
1516057 CIFC26 H15 Mo O5 PP 1 21 117.039; 6.2992; 21.025
90; 97.831; 90
2235.6Mao, Yanli; Lim, Kelvin Meng Hui; Ganguly, Rakesh; Mathey, Francois
A new route to a 2-phosphanaphthalene.
Organic letters, 2012, 14, 4974-4975
1516058 CIFC26 H16 Cl O6 P WP 1 21/c 118.4823; 9.4251; 15.2278
90; 114.313; 90
2417.38Mao, Yanli; Lim, Kelvin Meng Hui; Ganguly, Rakesh; Mathey, Francois
A new route to a 2-phosphanaphthalene.
Organic letters, 2012, 14, 4974-4975
1516059 CIFC26 H16 Cl O6 P WP 1 21/n 18.1251; 12.1902; 25.1571
90; 90.472; 90
2491.6Mao, Yanli; Lim, Kelvin Meng Hui; Ganguly, Rakesh; Mathey, Francois
A new route to a 2-phosphanaphthalene.
Organic letters, 2012, 14, 4974-4975
1516060 CIFC16 H20 N2 O3P n a 2140.076; 5.5575; 13.021
90; 90; 90
2900.1Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516061 CIFC17 H22 N2 O3P b c a9.5653; 10.45; 30.655
90; 90; 90
3064.2Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516062 CIFC16 H20 N2 O3P 1 21/n 110.604; 10.38; 13.204
90; 95.551; 90
1446.5Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516063 CIFC12 H12 N2 O2P 1 21/c 16.4277; 10.169; 15.7788
90; 95.698; 90
1026.26Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516064 CIFC15 H19 N OI b a 210.9646; 34.3413; 6.972
90; 90; 90
2625.23Brawn, Ryan A.; Guimarães, Cristiano R W; McClure, Kim F.; Liras, Spiros
An efficient synthesis of bridged heterocycles from an Ir(I) bis-amination/ring-closing metathesis sequence.
Organic letters, 2012, 14, 4802-4805
1516066 CIFC19 H25 N3 O2P 1 21/c 110.5786; 10.5791; 15.5501
90; 104.447; 90
1685.22Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A.
Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine.
Organic letters, 2012, 14, 5621-5623
1516067 CIFC20 H29 N3 O2P 1 21/c 111.8836; 10.3003; 15.9702
90; 109.242; 90
1845.62Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A.
Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine.
Organic letters, 2012, 14, 5621-5623
1516068 CIFC19 H26 N2 OP n a 2113.7232; 14.9269; 7.6655
90; 90; 90
1570.24Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A.
Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine.
Organic letters, 2012, 14, 5621-5623
1516069 CIFC21 H38 O4P 21 21 215.2688; 7.4978; 52.786
90; 90; 90
2085.28Persich, Peter; Kerschbaumer, Julia; Helling, Sandra; Hildmann, Barbara; Wibbeling, Birgit; Haufe, Günter
Transannular O-heterocyclization: a useful tool for the total synthesis of Murisolin and 16,19-cis-Murisolin.
Organic letters, 2012, 14, 5628-5631
1516074 CIFC40 H41 N3 O4P -112.3712; 12.5383; 13.3489
102.471; 100.682; 118.295
1677.5Castellano, Teresa G.; Neo, Ana G.; Marcaccini, Stefano; Marcos, Carlos F.
Enols as feasible acid components in the Ugi condensation.
Organic letters, 2012, 14, 6218-6221
1516075 CIFC19 H24 N2 O3P 21 21 217.9485; 12.166; 17.196
90; 90; 90
1662.9Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516076 CIFC20 H22 N2 O6P 21 21 217.1383; 10.9101; 23.798
90; 90; 90
1853.4Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516077 CIFC21 H26 N2 O5P 618.268; 8.268; 48.704
90; 90; 120
2883.3Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516078 CIFC21 H28 N2 O3P 21 21 217.4222; 9.96; 25.642
90; 90; 90
1895.6Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516079 CIFC22 H26 N2 O4P 21 21 217.9567; 12.3012; 20.572
90; 90; 90
2013.5Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516081 CIFC14 H17 B F2 N4P -17.3413; 7.5696; 13.1377
96.128; 99.18; 95.256
712.2Lee, Ho Yong; Olasz, András; Chen, Chun-Hsing; Lee, Dongwhan
Three-stage binary switching of azoaromatic polybase.
Organic letters, 2012, 14, 6286-6289
1516082 CIFC29 H20 N2 O7P -110.6771; 13.0878; 18.3378
83.667; 73.144; 75.898
2376.35Kelgtermans, Hans; Dobrzańska, Liliana; Van Meervelt, Luc; Dehaen, Wim
A fragment-based approach toward substituted trioxa[7]helicenes.
Organic letters, 2012, 14, 5200-5203
1516083 CIFC32 H38 O8P 1 21/c 16.0458; 9.8845; 24.023
90; 95.05; 90
1430Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516084 CIFC40 H54 O8P 1 21/c 116.6322; 9.1956; 12.1051
90; 98.357; 90
1831.73Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516085 CIFC26 H24 O8P 1 21/n 15.271; 14.1093; 15.2301
90; 94.765; 90
1128.7Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516086 CIFC24 H20 O8P 1 21/c 110.8267; 9.5361; 20.2199
90; 97.858; 90
2068Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516087 CIFC6 H5 Br O3P 1 21/n 110.3165; 4.9709; 14.1637
90; 101.925; 90
710.67Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516088 CIFC36 H42 O6C 1 2/c 129.11; 9.5418; 22.962
90; 103.062; 90
6212.9Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516089 CIFC32 H26 O8P 1 21/c 19.5983; 5.4838; 24.21
90; 91.793; 90
1273.7Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516090 CIFC26 H26 O8P 1 21/n 17.7228; 11.0389; 13.6925
90; 97.28; 90
1157.89Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516091 CIFC40 H52 O8P -15.7869; 9.9739; 16.9218
87.166; 81.47; 78.248
945.45Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516092 CIFC12 H12 Br2 O6P 1 21/n 19.6055; 7.7143; 18.8681
90; 93.576; 90
1395.4Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516093 CIFC40 H54 O12P -15.9676; 9.4094; 17.2733
89.735; 85.714; 85.834
964.7Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516094 CIFC32 H26 O8P -16.1693; 9.7194; 11.3573
67.533; 80.008; 86.414
619.77Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516095 CIFC32 H38 O12P -15.946; 10.5168; 12.6676
81.198; 80.39; 81.904
766.41Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516097 CIFC11 H12 O5C 1 c 110.4253; 12.8651; 8.1381
90; 109.962; 90
1025.92Barradas, Silvia; Hernández-Torres, Gloria; Urbano, Antonio; Carreño, M Carmen
Total synthesis of natural p-quinol cochinchinenone.
Organic letters, 2012, 14, 5952-5955
1516099 CIFC23 H20 N2 OP 1 21 16.4088; 17.279; 8.579
90; 101.67; 90
930.4Cai, Zhong-Jian; Wang, Shun-Yi; Ji, Shun-Jun
CuI/BF3·Et2O cocatalyzed aerobic dehydrogenative reactions of ketones with benzylamines: facile synthesis of substituted imidazoles.
Organic letters, 2012, 14, 6068-6071
1516100 CIFC22 H18 N2P 1 21/n 19.768; 11.392; 15.15
90; 97.216; 90
1672.5Cai, Zhong-Jian; Wang, Shun-Yi; Ji, Shun-Jun
CuI/BF3·Et2O cocatalyzed aerobic dehydrogenative reactions of ketones with benzylamines: facile synthesis of substituted imidazoles.
Organic letters, 2012, 14, 6068-6071
1516101 CIFC20 H18 O5P 1 21/n 116.4332; 5.5136; 18.3321
90; 106.549; 90
1592.2Truong, Phong; Shanahan, Charles S.; Doyle, Michael P.
Divergent stereocontrol of acid catalyzed intramolecular aldol reactions of 2,3,7-triketoesters: synthesis of highly functionalized cyclopentanones.
Organic letters, 2012, 14, 3608-3611
1516103 CIFC18 H24 N2 OP b c n18.945; 8.6958; 20.3655
90; 90; 90
3355.1Zhao, Shu-Bin; Bilodeau, Eric; Lemieux, Valérie; Beauchemin, André M
Hydrogen bonding directed intermolecular Cope-type hydroamination of alkenes.
Organic letters, 2012, 14, 5082-5085
1516104 CIFC30 H28 Cl N O4 SP -110.0293; 16.6704; 17.4029
70.567; 76.603; 78.855
2647.7Hu, Jian; Tian, Bing; Wu, Xinyan; Tong, Xiaofeng
Tertiary amine-triggered cascade S(N)2/cycloaddition: an efficient construction of complex azaheterocycles under mild conditions.
Organic letters, 2012, 14, 5074-5077
1516105 CIFC22 H26 N2 O6P 1 21/n 111.618; 12.024; 16.15
90; 110.574; 90
2112.2Villa, Reymundo A.; Xu, Qihai; Kwon, Ohyun
Total synthesis of (±)-hirsutine: application of phosphine-catalyzed imine-allene [4 + 2] annulation.
Organic letters, 2012, 14, 4634-4637
1516106 CIFC13 H15 N OC 1 2/c 114.0539; 11.358; 13.4342
90; 101.523; 90
2101.2Li, Xiao-Jing; Qiao, Jin-Bao; Sun, Jian; Li, Xue-Qiang; Gu, Peiming
Intramolecular Schmidt Reaction of Acyl Chlorides with Alkyl Azides: Capture of N-Acyliminium Ion Intermediates with Aromatic rings.
Organic letters, 2014, 16, 2865-2867
1516113 CIFC11 H12 F N O2P 1 21/n 111.272; 5.8049; 16.158
90; 108.477; 90
1002.8Lu, Deng-Fu; Liu, Guan-Sai; Zhu, Cheng-Liang; Yuan, Bo; Xu, Hao
Iron(II)-Catalyzed Intramolecular Olefin Aminofluorination.
Organic letters, 2014, 16, 2912-2915
1516114 CIFC72 H23 N O8P -110.128; 10.497; 20.664
85.27; 77.477; 78.869
2102.4Hashikawa, Yoshifumi; Murata, Michihisa; Wakamiya, Atsushi; Murata, Yasujiro
Synthesis of open-cage ketolactam derivatives of fullerene c60 encapsulating a hydrogen molecule.
Organic letters, 2014, 16, 2970-2973
1516121 CIFC15 H11 N O3P -15.502; 21.052; 21.138
88.513; 82.982; 85.62
2423Wu, Xia; Gao, Qinghe; Liu, Shan; Wu, Anxin
I2-Catalyzed Oxidative Cross-Coupling of Methyl Ketones and Benzamidines Hydrochloride: A Facile Access to α-Ketoimides.
Organic letters, 2014, 16, 2888-2891
1516122 CIFC58 H36 O4P -112.469; 14.085; 14.436
114.938; 101.497; 98.755
2171.7Wackerly, Jay Wm; Zhang, Mengfei; Nodder, Stephen T.; Carlin, Stephen M.; Katz, Jeffrey L.
Single Step Synthesis of Acetylene-Substituted Oxacalix[4]arenes.
Organic letters, 2014, 16, 2920-2922
1516129 CIFC37 H34 N2 O6 S2P 1 21/c 117.511; 10.814; 23.711
90; 130.536; 90
3412.4Nayak, Sanatan; Ghosh, Nayan; Sahoo, Akhila K.
Access to Cyclobutene-Fused Azepines through Au-Catalyzed Cycloisomerization of Stable Alkyne Tethered Ketene N,N-Acetals.
Organic letters, 2014, 16, 2996-2999
1516130 CIFC39 H32 N4 O6 S2A b a 215.0516; 28.646; 18.0316
90; 90; 90
7774.7Nayak, Sanatan; Ghosh, Nayan; Sahoo, Akhila K.
Access to Cyclobutene-Fused Azepines through Au-Catalyzed Cycloisomerization of Stable Alkyne Tethered Ketene N,N-Acetals.
Organic letters, 2014, 16, 2996-2999
1516131 CIFC39 H38 N2 O8 S2P -18.7849; 12.6893; 16.278
85.618; 79.626; 82.116
1765.6Nayak, Sanatan; Ghosh, Nayan; Sahoo, Akhila K.
Access to Cyclobutene-Fused Azepines through Au-Catalyzed Cycloisomerization of Stable Alkyne Tethered Ketene N,N-Acetals.
Organic letters, 2014, 16, 2996-2999
1516132 CIFC19 H14 Br N2 O0.5 SC 1 2/c 111.406; 14.522; 20.97
90; 104.457; 90
3363.4Ravi, Chitrakar; Chandra Mohan, Darapaneni; Adimurthy, Subbarayappa
N-chlorosuccinimide-promoted regioselective sulfenylation of imidazoheterocycles at room temperature.
Organic letters, 2014, 16, 2978-2981
1516133 CIFC20 H4 Br4 Cl4P c a 217.4442; 27.2175; 19.194
90; 90; 90
3888.9Zagranyarski, Yulian; Chen, Long; Jänsch, Daniel; Gessner, Thomas; Li, Chen; Müllen, Klaus
Toward perylene dyes by the hundsdiecker reaction.
Organic letters, 2014, 16, 2814-2817
1516134 CIFC19 H27 N O2 S SiP 1 21 19.154; 16.606; 13.184
90; 91.919; 90
2003Mita, Tsuyoshi; Sugawara, Masumi; Saito, Keisuke; Sato, Yoshihiro
Catalytic Enantioselective Silylation of N-Sulfonylimines: Asymmetric Synthesis of α-Amino Acids from CO2 via Stereospecific Carboxylation of α-Amino Silanes.
Organic letters, 2014, 16, 3028-3031
1516135 CIFC14 H25 N O2 S SnP 1 21 111.1188; 10.5531; 15.6491
90; 110.738; 90
1717.26Mita, Tsuyoshi; Sugawara, Masumi; Saito, Keisuke; Sato, Yoshihiro
Catalytic Enantioselective Silylation of N-Sulfonylimines: Asymmetric Synthesis of α-Amino Acids from CO2 via Stereospecific Carboxylation of α-Amino Silanes.
Organic letters, 2014, 16, 3028-3031
1516147 CIFC7 H9 Br O2P 3217.8119; 17.8119; 6.2589
90; 90; 120
1719.7Zipfel, Hannes F.; Carreira, Erick M.
An efficient synthesis strategy to the core structure of 6-5-6-5-6-membered epipolythiodiketopiperazines.
Organic letters, 2014, 16, 2854-2857
1516148 CIFC21 H24 N2 O4 SP 1 21 111.639; 5.5765; 15.5447
90; 106.278; 90
968.48Zipfel, Hannes F.; Carreira, Erick M.
An efficient synthesis strategy to the core structure of 6-5-6-5-6-membered epipolythiodiketopiperazines.
Organic letters, 2014, 16, 2854-2857
1516149 CIFC32.5 H31 Cl N2 O6C 1 2 143.265; 15.0547; 10.2366
90; 93.976; 90
6651.5Zipfel, Hannes F.; Carreira, Erick M.
An efficient synthesis strategy to the core structure of 6-5-6-5-6-membered epipolythiodiketopiperazines.
Organic letters, 2014, 16, 2854-2857
1516152 CIFC16 H13 Br O3P 1 21 17.952; 12.184; 14.721
90; 92.596; 90
1424.8Fu, Liangbing; Wang, Hengbin; Davies, Huw M. L.
Role of Ortho-Substituents on Rhodium-Catalyzed Asymmetric Synthesis of β-Lactones by Intramolecular C-H Insertions of Aryldiazoacetates.
Organic letters, 2014, 16, 3036-3039
1516153 CIFC11 H11 Br O3P 21 21 2112.06; 12.066; 14.641
90; 90; 90
2130.5Fu, Liangbing; Wang, Hengbin; Davies, Huw M. L.
Role of Ortho-Substituents on Rhodium-Catalyzed Asymmetric Synthesis of β-Lactones by Intramolecular C-H Insertions of Aryldiazoacetates.
Organic letters, 2014, 16, 3036-3039
1516154 CIFC10 H9 Br O3P 1 21 16.2085; 5.3383; 15.239
90; 95.715; 90
502.6Fu, Liangbing; Wang, Hengbin; Davies, Huw M. L.
Role of Ortho-Substituents on Rhodium-Catalyzed Asymmetric Synthesis of β-Lactones by Intramolecular C-H Insertions of Aryldiazoacetates.
Organic letters, 2014, 16, 3036-3039
1516169 CIFC10 H8 B2 F4 N4C 1 2/m 112.2662; 6.8136; 7.0499
90; 105.816; 90
566.9Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong
Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole.
Organic letters, 2014, 16, 3048-3051
1516170 CIFC14 H16 B2 F4 N4P 1 21/c 19.2147; 12.1024; 7.3238
90; 108.772; 90
773.3Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong
Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole.
Organic letters, 2014, 16, 3048-3051
1516171 CIFC18 H24 B2 F4 N4P 1 21/n 19.676; 13.659; 15.313
90; 103.66; 90
1966.6Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong
Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole.
Organic letters, 2014, 16, 3048-3051
1516172 CIFC10 H9 B F2 N4P b c a12.306; 9.48; 18.766
90; 90; 90
2189.3Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong
Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole.
Organic letters, 2014, 16, 3048-3051
1516173 CIFC14 H17 B F2 N4P 1 21/c 18.058; 21.225; 8.7995
90; 102.217; 90
1470.9Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong
Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole.
Organic letters, 2014, 16, 3048-3051
1516174 CIFC26 H22 F6 N4 O4C 1 2/c 129.895; 12.375; 15.464
90; 107.104; 90
5468Zhang, Fa-Guang; Wei, Yi; Yi, Yu-Ping; Nie, Jing; Ma, Jun-An
Regioselective Cycloaddition of Trifluorodiazoethane with Electron-Deficient Allenic Esters and Ketones: Access to CF3-Substituted Pyrazolines and Pyrazoles.
Organic letters, 2014, 16, 3122-3125
1516175 CIFC15 H18 N2 O3P 1 21/n 19.4197; 8.3092; 17.992
90; 98.7; 90
1392Cai, Shangjun; Chen, Chao; Shao, Peng; Xi, Chanjuan
Rh(III)-Catalyzed Cascade Oxidative Olefination/Cyclization of Picolinamides and Alkenes via C-H Activation.
Organic letters, 2014, 16, 3142-3145
1516176 CIFC14 H16 N2 O3P 1 21/c 17.5875; 21.568; 8.3245
90; 110.26; 90
1278Cai, Shangjun; Chen, Chao; Shao, Peng; Xi, Chanjuan
Rh(III)-Catalyzed Cascade Oxidative Olefination/Cyclization of Picolinamides and Alkenes via C-H Activation.
Organic letters, 2014, 16, 3142-3145
1516232 CIFC82.5 H44 F15 N OP -114.729; 15.302; 17.015
110.482; 91.5392; 117.76
3094.5Chou, Chih-Ming; Saito, Shohei; Yamaguchi, Shigehiro
Heterotriangulenes π-Expanded at Bridging Positions.
Organic letters, 2014, 16, 2868-2871
1516233 CIFC122.4 H59 Cl3.4 F15 NP -126.3661; 26.5069; 39.8191
100.01; 99.1855; 99.1177
26552.9Chou, Chih-Ming; Saito, Shohei; Yamaguchi, Shigehiro
Heterotriangulenes π-Expanded at Bridging Positions.
Organic letters, 2014, 16, 2868-2871
1516234 CIFC78 H32 F15 NC 1 2/c 125.7374; 16.733; 30.152
90; 114.227; 90
11841.7Chou, Chih-Ming; Saito, Shohei; Yamaguchi, Shigehiro
Heterotriangulenes π-Expanded at Bridging Positions.
Organic letters, 2014, 16, 2868-2871
1516235 CIFC13 H16 O6P b c a11.5879; 11.617; 19.7761
90; 90; 90
2662.19Rout, Saroj Kumar; Guin, Srimanta; Ali, Wajid; Gogoi, Anupal; Patel, Bhisma K.
Copper-Catalyzed Esterification of Alkylbenzenes with Cyclic Ethers and Cycloalkanes via C(sp(3))-H Activation Following Cross-Dehydrogenative Coupling.
Organic letters, 2014, 16, 3086-3089
1516236 CIFC49 H36 O5P 1 2/n 19.772; 12.0351; 17.3162
90; 93.947; 90
2031.68Nandakumar, Meganathan; Karunakaran, Jayachandran; Mohanakrishnan, Arasambattu K.
Diels-Alder Reaction of 1,3-Diarylbenzo[c]furans with Thiophene S,S-Dioxide/Indenone Derivatives: A Facile Preparation of Substituted Dibenzothiophene S,S-Dioxides and Fluorenones.
Organic letters, 2014, 16, 3068-3071
1516237 CIFC34 H24 O4 SP -113.7369; 13.8077; 16.4824
78.442; 68.211; 80.216
2828.35Nandakumar, Meganathan; Karunakaran, Jayachandran; Mohanakrishnan, Arasambattu K.
Diels-Alder Reaction of 1,3-Diarylbenzo[c]furans with Thiophene S,S-Dioxide/Indenone Derivatives: A Facile Preparation of Substituted Dibenzothiophene S,S-Dioxides and Fluorenones.
Organic letters, 2014, 16, 3068-3071
1516238 CIFC28 H18 O2 SP 1 21/n 19.9374; 16.1534; 13.053
90; 100.308; 90
2061.49Nandakumar, Meganathan; Karunakaran, Jayachandran; Mohanakrishnan, Arasambattu K.
Diels-Alder Reaction of 1,3-Diarylbenzo[c]furans with Thiophene S,S-Dioxide/Indenone Derivatives: A Facile Preparation of Substituted Dibenzothiophene S,S-Dioxides and Fluorenones.
Organic letters, 2014, 16, 3068-3071
1516262 CIFC20 H38 Au Cl4 N5P -18.9016; 12.934; 13.6174
63.626; 78.563; 80.061
1370.35Mirabdolbaghi, Roya; Dudding, Travis; Stamatatos, Theocharis
A Class of Phase-Transfer Catalyst with Interionic Strain: Insight into the Bonding of Disubstituted N- vs Carbene-Stabilized N(I)-Centered Cations.
Organic letters, 2014, 16, 2790-2793
1516263 CIFC26 H41 Cl F9 N5 O6P 1 21/c 116.646; 22.121; 9.329
90; 90.328; 90
3435.1Mirabdolbaghi, Roya; Dudding, Travis; Stamatatos, Theocharis
A Class of Phase-Transfer Catalyst with Interionic Strain: Insight into the Bonding of Disubstituted N- vs Carbene-Stabilized N(I)-Centered Cations.
Organic letters, 2014, 16, 2790-2793
1516264 CIFC24 H25 Cl N2 O4P 21 21 2111.939; 12.451; 15.057
90; 90; 90
2238.3Zhang, Han-Ming; Gao, Zhong-Hua; Ye, Song
Bifunctional N-Heterocyclic Carbene-Catalyzed Highly Enantioselective Synthesis of Spirocyclic Oxindolo-β-lactams.
Organic letters, 2014, 16, 3079-3081
1516265 CIFC24 H16 N2 OP b c a14.7042; 8.8119; 27.6407
90; 90; 90
3581.46Dong, Jiaxing; Wang, Fei; You, Jingsong
Copper-Mediated Tandem Oxidative C(sp(2))-H/C(sp)-H Alkynylation and Annulation of Arenes with Terminal Alkynes.
Organic letters, 2014, 16, 2884-2887
1516325 CIFC9 H10 N O3 PP 1 21/n 16.877; 16.165; 8.684
90; 107.06; 90
922.9Kim, Yea Rin; Cho, Seungyoon; Lee, Phil Ho
Metal-Free Azaphosphaannulation of Phosphonamides through Intramolecular Oxidative C-N Bond Formation.
Organic letters, 2014, 16, 3098-3101
1516326 CIFC10 H12 N O3 PP 1 21/c 17.203; 8.501; 17.051
90; 90.9; 90
1044Kim, Yea Rin; Cho, Seungyoon; Lee, Phil Ho
Metal-Free Azaphosphaannulation of Phosphonamides through Intramolecular Oxidative C-N Bond Formation.
Organic letters, 2014, 16, 3098-3101
1516339 CIFC12 H15 N O3P 1 21 18.4867; 6.5654; 11.1325
90; 108.878; 90
586.92Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A.
General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis.
Organic letters, 2014, 16, 3166-3169
1516340 CIFC7 H11 N O4P 21 21 215.8815; 8.9902; 15.9025
90; 90; 90
840.86Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A.
General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis.
Organic letters, 2014, 16, 3166-3169
1516341 CIFC14 H29 Cl N2 O3P 1 21/c 18.9297; 13.194; 14.536
90; 98.9222; 90
1691.89Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A.
General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis.
Organic letters, 2014, 16, 3166-3169
1516342 CIFC14 H17 Cl2 N2 O3P 1 21/c 114.922; 11.523; 9.548
90; 98.829; 90
1622Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A.
General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis.
Organic letters, 2014, 16, 3166-3169
1516343 CIFC19 H24 N2 O2P 1 21/c 113.7462; 11.9167; 12.602
90; 106.292; 90
1981.4Tian, Jingjing; Du, Qiuchen; Guo, Rui; Li, Yun; Cheng, Bin; Zhai, Hongbin
Total synthesis of indole alkaloid (±)-subincanadine e.
Organic letters, 2014, 16, 3173-3175
1516457 CIFC14 H19 N O2 SP 1 21 17.3662; 17.2624; 11.3119
90; 107.957; 90
1368.33Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo
Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines.
Organic letters, 2014, 16, 3162-3165
1516458 CIFC15 H21 N O2 SP 21 21 217.6766; 17.0877; 22.6809
90; 90; 90
2975.2Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo
Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines.
Organic letters, 2014, 16, 3162-3165
1516459 CIFC19 H21 N O2 SP 21 21 219.7947; 9.9666; 16.9986
90; 90; 90
1659.4Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo
Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines.
Organic letters, 2014, 16, 3162-3165
1516460 CIFC15 H23 N O2 SP 1 21 110.2019; 13.2716; 11.3946
90; 100.893; 90
1515Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo
Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines.
Organic letters, 2014, 16, 3162-3165
1516461 CIFC29 H23 N5 O2 SP -19.4716; 10.8769; 11.9856
83.113; 83.385; 87.083
1216.8Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki
Gold-Catalyzed Cascade Cyclization of (Azido)ynamides: An Efficient Strategy for the Construction of Indoloquinolines.
Organic letters, 2014, 16, 3138-3141
1516462 CIFC29 H22 N2 O2 SP b c a19.6725; 18.2791; 12.5149
90; 90; 90
4500.3Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki
Gold-Catalyzed Cascade Cyclization of (Azido)ynamides: An Efficient Strategy for the Construction of Indoloquinolines.
Organic letters, 2014, 16, 3138-3141
1516464 CIFC26 H30 Cl N2 O4C 1 2 121.651; 8.9952; 13.072
90; 92.662; 90
2543.1Xu, Jianfeng; Mou, Chengli; Zhu, Tingshun; Song, Bao-An; Chi, Yonggui Robin
N-heterocyclic carbene-catalyzed chemoselective cross-aza-benzoin reaction of enals with isatin-derived ketimines: access to chiral quaternary aminooxindoles.
Organic letters, 2014, 16, 3272-3275
1516477 CIFC18 H18 Br N O4 SP 1 21/c 112.50619; 11.55718; 12.58675
90; 97.3759; 90
1804.19Medina, Florian; Besnard, Céline; Lacour, Jérôme
One-Step Synthesis of Nitrogen-Containing Medium-Sized Rings via α-Imino Diazo Intermediates.
Organic letters, 2014, 16, 3232-3235
1516478 CIFC17 H16 Br N O4 SP 1 21/a 112.4111; 11.2306; 12.7572
90; 98.363; 90
1759.24Medina, Florian; Besnard, Céline; Lacour, Jérôme
One-Step Synthesis of Nitrogen-Containing Medium-Sized Rings via α-Imino Diazo Intermediates.
Organic letters, 2014, 16, 3232-3235
1516498 CIFC34 H28 N2 O4P b c a16.1351; 15.7795; 21.2316
90; 90; 90
5405.6Frischmann, Peter D.; Jiang, Jian; Hui, Joseph K.-H.; Grzybowski, Joseph J.; MacLachlan, Mark J.
Reversible-irreversible approach to Schiff base macrocycles: access to isomeric macrocycles with multiple salphen pockets.
Organic letters, 2008, 10, 1255-1258
1516499 CIFC38 H36 P2 S2P 1 21/c 110.201; 19.08; 16.886
90; 98.7827; 90
3248Furukawa, Shunsuke; Haga, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki
Synthesis of π-Extended Dibenzophospholes by Intramolecular Radical Cyclization and Their Properties.
Organic letters, 2014, 16, 3228-3231
1516500 CIFC38 H36 P2 S2P -19.151; 12.814; 15.408
109.378; 91.446; 107.726
1607.4Furukawa, Shunsuke; Haga, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki
Synthesis of π-Extended Dibenzophospholes by Intramolecular Radical Cyclization and Their Properties.
Organic letters, 2014, 16, 3228-3231
1516501 CIFC23 H23 N O6P 21 21 217.4232; 16.138; 16.7378
90; 90; 90
2005.11Xiao, You-Cai; Yue, Cai-Zhen; Chen, Peng-Qiao; Chen, Ying-Chun
Asymmetric Dearomatic Diels-Alder Reactions of Diverse Heteroarenes via π-System Activation.
Organic letters, 2014, 16, 3208-3211
1516517 CIFC15 H15 N O2P 1 21/n 110.2481; 10.1664; 12.1731
90; 93.195; 90
1266.3Zhang, Zhi-Jing; Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui
A Facile BPO-Mediated ortho-Hydroxylation and Benzoylation of N-Alkyl Anilines for Synthesis of 2-Benzamidophenols.
Organic letters, 2014, 16, 3292-3295
1516518 CIFC14 H13 N O2P 1 21/c 18.226; 11.711; 13.239
90; 106.88; 90
1220.4Zhang, Zhi-Jing; Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui
A Facile BPO-Mediated ortho-Hydroxylation and Benzoylation of N-Alkyl Anilines for Synthesis of 2-Benzamidophenols.
Organic letters, 2014, 16, 3292-3295
1516522 CIFC26 H31 N O5P 21 21 217.495; 10.4454; 35.197
90; 90; 90
2755.5Letort, Aurélien; Aouzal, Rémi; Ma, Cong; Long, De-Liang; Prunet, Joëlle
Highly efficient synthesis of the tricyclic core of taxol by cascade metathesis.
Organic letters, 2014, 16, 3300-3303
1516523 CIFC15 H18 N2 O2P 1 21 16.546; 12.058; 8.846
90; 97.94; 90
691.5Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko
Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones.
Organic letters, 2014, 16, 3348-3351
1516524 CIFC24 H20 O2P 21 21 218.9315; 9.1942; 21.867
90; 90; 90
1795.7Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko
Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones.
Organic letters, 2014, 16, 3348-3351
1516525 CIFC35 H34 N2 O3P 21 21 218.284; 13.944; 23.978
90; 90; 90
2770Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko
Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones.
Organic letters, 2014, 16, 3348-3351
1516526 CIFC28 H30 N2 O3P 16.63; 8.27; 22.07
89.6; 87.7; 80
1191Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko
Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones.
Organic letters, 2014, 16, 3348-3351
1516527 CIFC19 H22 N2 O4P 1 21/c 17.297; 12.192; 19.971
90; 94.898; 90
1770.2Patel, Pitambar; Chang, Sukbok
N-substituted hydroxylamines as synthetically versatile amino sources in the iridium-catalyzed mild C-h amidation reaction.
Organic letters, 2014, 16, 3328-3331
1516528 CIFC26 H29 F3 Ir N O4P 1 21/n 116.479; 8.855; 17.7803
90; 103.143; 90
2526.6Patel, Pitambar; Chang, Sukbok
N-substituted hydroxylamines as synthetically versatile amino sources in the iridium-catalyzed mild C-h amidation reaction.
Organic letters, 2014, 16, 3328-3331
1516529 CIFC20 H20 N2 O2P 1 21/n 19.508; 10.4245; 17.1939
90; 98.397; 90
1685.92Patel, Pitambar; Chang, Sukbok
N-substituted hydroxylamines as synthetically versatile amino sources in the iridium-catalyzed mild C-h amidation reaction.
Organic letters, 2014, 16, 3328-3331
1516574 CIFC22 H18 I N3 O4 SP 21 21 217.7904; 14.7; 19.469
90; 90; 90
2229.6Tripathi, Chandra Bhushan; Mukherjee, Santanu
Catalytic enantioselective iodoaminocyclization of hydrazones.
Organic letters, 2014, 16, 3368-3371
1516579 CIFC22 H25 N2 O4 S2P -16.6422; 8.0514; 20.8031
89.74; 87.881; 83.068
1103.64Zhang, Jie; Shao, Ying; Wang, Hongxiang; Luo, Qiang; Chen, Jijun; Xu, Dongmei; Wan, Xiaobing
Dual Roles of Sulfonyl Hydrazides: A Three-Component Reaction To Construct Fully Substituted Pyrazoles Using TBAI/TBHP.
Organic letters, 2014, 16, 3312-3315
1516580 CIFC24 H12 S2P 1 21/c 112.0564; 12.1122; 12.1107
90; 110.407; 90
1657.5Xiong, Xiao-Dong; Deng, Chun-Lin; Peng, Xiao-Shui; Miao, Qian; Wong, Henry N. C.
Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties.
Organic letters, 2014, 16, 3252-3255
1516581 CIFC24 H12 Se4P 1 21/c 112.7769; 20.4663; 16.3532
90; 109.347; 90
4034.8Xiong, Xiao-Dong; Deng, Chun-Lin; Peng, Xiao-Shui; Miao, Qian; Wong, Henry N. C.
Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties.
Organic letters, 2014, 16, 3252-3255
1516582 CIFC38 H26 N2P 1 21/n 110.4127; 18.6669; 13.9771
90; 107.068; 90
2597.1Xiong, Xiao-Dong; Deng, Chun-Lin; Peng, Xiao-Shui; Miao, Qian; Wong, Henry N. C.
Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties.
Organic letters, 2014, 16, 3252-3255
1516583 CIFC24 H8 O2P m m n :212.3385; 15.6948; 3.8193
90; 90; 90
739.61Xiong, Xiao-Dong; Deng, Chun-Lin; Peng, Xiao-Shui; Miao, Qian; Wong, Henry N. C.
Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties.
Organic letters, 2014, 16, 3252-3255
1516584 CIFC24 H12 Se2P b c n28.5952; 7.5369; 15.6922
90; 90; 90
3382Xiong, Xiao-Dong; Deng, Chun-Lin; Peng, Xiao-Shui; Miao, Qian; Wong, Henry N. C.
Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties.
Organic letters, 2014, 16, 3252-3255
1516585 CIFC36 H22 N2C 1 2/c 118.0254; 10.3777; 12.614
90; 101.085; 90
2315.6Xiong, Xiao-Dong; Deng, Chun-Lin; Peng, Xiao-Shui; Miao, Qian; Wong, Henry N. C.
Heteroatom-bridged tetraphenylenes: synthesis, structures, and properties.
Organic letters, 2014, 16, 3252-3255
1516586 CIFC34 H45 Br N2 O6 SiP -18.0482; 14.1277; 15.3665
99.073; 94.101; 91.448
1719.75Han, Seo-Jung; Vogt, Florian; Krishnan, Shyam; May, Jeremy A.; Gatti, Michele; Virgil, Scott C.; Stoltz, Brian M.
A diastereodivergent synthetic strategy for the syntheses of communesin f and perophoramidine.
Organic letters, 2014, 16, 3316-3319
1516587 CIFC22 H19 Br N2 O5P 21 21 219.1581; 12.6857; 16.703
90; 90; 90
1940.5Han, Seo-Jung; Vogt, Florian; Krishnan, Shyam; May, Jeremy A.; Gatti, Michele; Virgil, Scott C.; Stoltz, Brian M.
A diastereodivergent synthetic strategy for the syntheses of communesin f and perophoramidine.
Organic letters, 2014, 16, 3316-3319
1516603 CIFC20 H20 B N OP 1 21/c 123.009; 5.4564; 13.699
90; 103.943; 90
1669.2Brown, Alec N.; Zakharov, Lev N.; Mikulas, Tanya; Dixon, David A.; Liu, Shih-Yuan
Rhodium-Catalyzed B-H Activation of 1,2-Azaborines: Synthesis and Characterization of BN Isosteres of Stilbenes.
Organic letters, 2014, 16, 3340-3343
1516604 CIFC21 H24 O3P 1 21/n 16.7908; 8.8056; 28.0909
90; 95.65; 90
1671.59Lee, Jihoon; Panek, James S.
Synthesis of Isochromene-Type Scaffolds via Single-Flask Diels-Alder-[4 + 2]-Annulation Sequence of a Silyl-Substituted Diene with Menadione.
Organic letters, 2014, 16, 3320-3323
1516606 CIFC30 H24P 1 21/n 110.58564; 6.27352; 16.626
90; 95.2712; 90
1099.45Horino, Yoshikazu; Takahashi, Yu; Koketsu, Kaori; Abe, Hitoshi; Tsuge, Kiyoshi
Practical and Convenient Synthesis of 1,6-Di- or 1,2,5,6-Tetra-arylhexa-1,3,5-trienes by the Dimerization of Pd(0)-Complexed Alkenylcarbenes Generated from π-Allylpalladium Intermediates.
Organic letters, 2014, 16, 3184-3187
1516607 CIFC11 H14 Br N O4 SP 21 21 216.8751; 8.4919; 22.997
90; 90; 90
1342.6Chen, Ya-Jing; Chen, Ya-Heng; Feng, Chen-Guo; Lin, Guo-Qiang
Enantioselective Rhodium-Catalyzed Arylation of Cyclic N-Sulfamidate Alkylketimines: A New Access to Chiral β-Alkyl-β-aryl Amino Alcohols.
Organic letters, 2014, 16, 3400-3403
1516608 CIFC19 H19 O5 PP 1 21/n 110.365; 11.372; 15.121
90; 96.49; 90
1770.9Mi, Xia; Wang, Chenyang; Huang, Mengmeng; Zhang, Jianye; Wu, Yusheng; Wu, Yangjie
Silver-Catalyzed Synthesis of 3-Phosphorated Coumarins via Radical Cyclization of Alkynoates and Dialkyl H-Phosphonates.
Organic letters, 2014, 16, 3356-3359
1516627 CIFC16 H14 Cl2P 21 21 215.6849; 7.6858; 32.425
90; 90; 90
1416.7Srinivas, Harathi D.; Zhou, Qi; Watson, Mary P.
Enantiospecific, nickel-catalyzed cross-couplings of allylic pivalates and arylboroxines.
Organic letters, 2014, 16, 3596-3599
1516628 CIFC10 H15 N O4 SP 21 21 216.5056; 8.2425; 21.78
90; 90; 90
1167.9Choudhary, Amit; Newberry, Robert W.; Raines, Ronald T.
n→π* Interactions Engender Chirality in Carbonyl Groups.
Organic letters, 2014, 16, 3421-3423
1516629 CIFC10 H15 N O4 SP 21 21 218.4606; 9.8014; 14.3985
90; 90; 90
1194.01Choudhary, Amit; Newberry, Robert W.; Raines, Ronald T.
n→π* Interactions Engender Chirality in Carbonyl Groups.
Organic letters, 2014, 16, 3421-3423
1516630 CIFC8 H13 N O3 SP 21 21 217.9045; 10.8117; 11.4208
90; 90; 90
976.03Choudhary, Amit; Newberry, Robert W.; Raines, Ronald T.
n→π* Interactions Engender Chirality in Carbonyl Groups.
Organic letters, 2014, 16, 3421-3423
1516631 CIFC9 H15 N O3 SP 1 21 16.3034; 6.8102; 12.5634
90; 99.245; 90
532.31Choudhary, Amit; Newberry, Robert W.; Raines, Ronald T.
n→π* Interactions Engender Chirality in Carbonyl Groups.
Organic letters, 2014, 16, 3421-3423
1516632 CIFC8 H13 N O3 SP 21 21 216.4374; 11.8996; 12.6886
90; 90; 90
971.98Choudhary, Amit; Newberry, Robert W.; Raines, Ronald T.
n→π* Interactions Engender Chirality in Carbonyl Groups.
Organic letters, 2014, 16, 3421-3423
1516633 CIFC9 H15 N O3 SC 1 2 114.493; 6.393; 11.849
90; 96.568; 90
1090.6Choudhary, Amit; Newberry, Robert W.; Raines, Ronald T.
n→π* Interactions Engender Chirality in Carbonyl Groups.
Organic letters, 2014, 16, 3421-3423
1516634 CIFC16 H14 O4P 21 21 218.7505; 9.3028; 15.4206
90; 90; 90
1255.3Li, Xin; Lin, Mao-Hui; Han, Yu; Wang, Feng; Cheng, Jin-Pei
Correction to Asymmetric Diels-Alder Reaction of 3-Olefinic Benzofuran-2-ones and Polyenals: Construction of Chiral Spirocyclic Benzofuran-2-ones.
Organic letters, 2014, 16, 3847
1516653 CIFC24 H33 N O6P 1 21 113.576; 8.049; 10.772
90; 109.89; 90
1106.9Li, Chun-Shun; Di, Ying-Tong; He, Hong-Ping; Gao, Suo; Wang, Yue-Hu; Lu, Yang; Zhong, Jia-Liang; Hao, Xiao-Jiang
Daphlongeranines A and B, two novel alkaloids possessing unprecedented skeletons from Daphniphyllum longeracemosum.
Organic letters, 2007, 9, 2509-2512
1516654 CIFC19 H34 F6 N2 O10 S2 ZnP 21 21 219.332; 12.2796; 25.7432
90; 90; 90
2950Monge, David; Martín-Zamora, Eloísa; Vazquez, Juan; Alcarazo, Manuel; Alvarez, Eleuterio; Fernandez, Rosario; Lassaletta, José M
Enantioselective conjugate addition of N,N-dialkylhydrazones to alpha-hydroxy enones.
Organic letters, 2007, 9, 2867-2870
1516655 CIFC53 H35 Cl3 N4 O2P -111.9304; 13.1965; 14.3418
85.259; 78.176; 79.079
2167.77Leung, Man-kit; Yang, Chih-Chiang; Lee, Jiun-Haw; Tsai, Hsin-Hung; Lin, Chi-Feng; Huang, Chih-Yen; Su, Yuhlong Oliver; Chiu, Chi-Feng
The unusual electrochemical and photophysical behavior of 2,2'-bis(1,3,4-oxadiazol-2-yl)biphenyls, effective electron transport hosts for phosphorescent organic light emitting diodes.
Organic letters, 2007, 9, 235-238
1516656 CIFC40 H26 N4 O2P 1 2/n 114.9947; 7.2016; 15.2457
90; 113.94; 90
1504.69Leung, Man-kit; Yang, Chih-Chiang; Lee, Jiun-Haw; Tsai, Hsin-Hung; Lin, Chi-Feng; Huang, Chih-Yen; Su, Yuhlong Oliver; Chiu, Chi-Feng
The unusual electrochemical and photophysical behavior of 2,2'-bis(1,3,4-oxadiazol-2-yl)biphenyls, effective electron transport hosts for phosphorescent organic light emitting diodes.
Organic letters, 2007, 9, 235-238
1516657 CIFC28 H18 N4 O2P b c n11.3862; 10.0904; 18.8335
90; 90; 90
2163.81Leung, Man-kit; Yang, Chih-Chiang; Lee, Jiun-Haw; Tsai, Hsin-Hung; Lin, Chi-Feng; Huang, Chih-Yen; Su, Yuhlong Oliver; Chiu, Chi-Feng
The unusual electrochemical and photophysical behavior of 2,2'-bis(1,3,4-oxadiazol-2-yl)biphenyls, effective electron transport hosts for phosphorescent organic light emitting diodes.
Organic letters, 2007, 9, 235-238
1516658 CIFC53 H33 Cl3 N6 O2P 1 2/c 111.0052; 13.4251; 14.8416
90; 102.384; 90
2141.76Leung, Man-kit; Yang, Chih-Chiang; Lee, Jiun-Haw; Tsai, Hsin-Hung; Lin, Chi-Feng; Huang, Chih-Yen; Su, Yuhlong Oliver; Chiu, Chi-Feng
The unusual electrochemical and photophysical behavior of 2,2'-bis(1,3,4-oxadiazol-2-yl)biphenyls, effective electron transport hosts for phosphorescent organic light emitting diodes.
Organic letters, 2007, 9, 235-238
1516659 CIFC18 H17 N O2P 1 21/c 112.063; 11.771; 11.209
90; 106.55; 90
1525.7Yang, Luo; Deng, Gang; Wang, De-Xian; Huang, Zhi-Tang; Zhu, Jie-Ping; Wang, Mei-Xiang
Highly efficient and stereoselective N-vinylation of oxiranecarboxamides and unprecedented 8-endo-epoxy-arene cyclization: expedient and biomimetic synthesis of some Clausena alkaloids.
Organic letters, 2007, 9, 1387-1390
1516660 CIFC28 H27 N O3 SP 1 21/c 111.1671; 16.1513; 13.1889
90; 95.155; 90
2369.2Tsuchikama, Kyoji; Kuwata, Yusuke; Tahara, Yu-ki; Yoshinami, Yusuke; Shibata, Takanori
Rh-catalyzed cyclization of diynes and enynes initiated by carbonyl-directed activation of aromatic and vinylic C-H bonds.
Organic letters, 2007, 9, 3097-3099
1516661 CIFC18 H21 N O3P 1 21/c 19.6928; 10.3932; 15.2434
90; 100.477; 90
1510.01Su, Shun; Porco, Jr, John A
1,2-dihydroisoquinolines as templates for cascade reactions to access isoquinoline alkaloid frameworks.
Organic letters, 2007, 9, 4983-4986
1516662 CIFC32 H44 O11P 1 21 18.2919; 18.2388; 10.7413
90; 106.478; 90
1557.7Yin, Sheng; Wang, Xiao-Ning; Fan, Cheng-Qi; Liao, Shang-Gao; Yue, Jian-Min
The first limonoid peroxide in the Meliaceae family: walsuronoid A from Walsura robusta.
Organic letters, 2007, 9, 2353-2356
1516663 CIFC13 H16 O3 SP 1 21 116.0338; 5.4918; 16.9616
90; 117.095; 90
1329.6Jung, Jae Hoon; Kim, Yong Wook; Kim, Min Ah; Choi, Soo Young; Chung, Young Keun; Kim, Tae-Rae; Shin, Seokmin; Lee, Eun
Efficient chirality transfer in the SmI2-mediated cyclization of aldehydo beta-alkoxyvinyl sulfoxides: asymmetric synthesis of 3-hydroxyoxanes.
Organic letters, 2007, 9, 3225-3228
1516664 CIFC22 H17 NC 1 2/c 116.4531; 12.9636; 15.6226
90; 102.578; 90
3252.2Han, Wenjia; Zhang, Guoying; Li, Guangxing; Huang, Hanmin
Rh-catalyzed sequential oxidative C-h and N-N bond activation: conversion of azines into isoquinolines with air at room temperature.
Organic letters, 2014, 16, 3532-3535
1516665 CIFC30 H36 O4P 1 21 110.7866; 7.7855; 14.9348
90; 99.41; 90
1237.33Tian, Wen-Jing; Yu, Yang; Yao, Xiao-Jun; Chen, Hai-Feng; Dai, Yi; Zhang, Xiao-Kun; Yao, Xin-Sheng
Norsampsones A-D, Four New Decarbonyl Polycyclic Polyprenylated Acylphloroglucinols from Hypericum sampsonii.
Organic letters, 2014, 16, 3448-3451
1516690 CIFC60 H52 N2 S4P 1 21/c 112.86; 26.508; 15.338
90; 110.628; 90
4893Karthik, Ganesan; Srinivasan, A.; Chandrashekar, Tavarekere K.
meso-Aryl Core-Modified Fused Sapphyrins: Syntheses and Structural Diversity.
Organic letters, 2014, 16, 3472-3475
1516691 CIFC18 H19 N O2P -110.9901; 11.6965; 13.3134
66.633; 67.953; 82.977
1455.43Zhao, Chen; Li, Ping; Smith, Mark D.; Pellechia, Perry J.; Shimizu, Ken D.
Experimental Study of the Cooperativity of CH-π Interactions.
Organic letters, 2014, 16, 3520-3523
1516692 CIFC42 H31 N O3P -110.1567; 12.264; 13.09
76.602; 73.82; 74.329
1486Zhao, Chen; Li, Ping; Smith, Mark D.; Pellechia, Perry J.; Shimizu, Ken D.
Experimental Study of the Cooperativity of CH-π Interactions.
Organic letters, 2014, 16, 3520-3523
1516693 CIFC43 H32 N2 O3P 1 21/n 110.6344; 13.5264; 22.2337
90; 94.961; 90
3186.2Zhao, Chen; Li, Ping; Smith, Mark D.; Pellechia, Perry J.; Shimizu, Ken D.
Experimental Study of the Cooperativity of CH-π Interactions.
Organic letters, 2014, 16, 3520-3523
1516694 CIFC43 H29 Cl2 N O3P 1 21/c 116.9467; 12.1612; 31.646
90; 97.377; 90
6468Zhao, Chen; Li, Ping; Smith, Mark D.; Pellechia, Perry J.; Shimizu, Ken D.
Experimental Study of the Cooperativity of CH-π Interactions.
Organic letters, 2014, 16, 3520-3523
1516703 CIFC16 H12 N2 O3P 1 21/n 19.8869; 8.4979; 17.1534
90; 103.026; 90
1404.1Zheng, Jing; Zhang, Yan; Cui, Sunliang
Rh(III)-Catalyzed Selective Coupling of N-Methoxy-1H-indole-1-carboxamides and Aryl Boronic Acids.
Organic letters, 2014, 16, 3560-3563
1516704 CIFC17 H22 Cl3 N O3P -17.1463; 10.177; 13.3296
99.67; 92.942; 99.295
940.04Manikandan, Rajendran; Jeganmohan, Masilamani
Ruthenium-catalyzed cyclization of anilides with substituted propiolates or acrylates: an efficient route to 2-quinolinones.
Organic letters, 2014, 16, 3568-3571
1516705 CIFC22 H21 N O2P 21 21 215.9003; 14.002; 21.7297
90; 90; 90
1795.22Yu, Yuanyuan; Wang, Chunyu; He, Xinze; Yao, Xiaotong; Zu, Liansuo
Efficient Assembly of Polysubstituted Pyrroles via a (3 + 2) Cycloaddition/Skeletal Rearrangement/Redox Isomerization Cascade Reaction.
Organic letters, 2014, 16, 3580-3583
1516706 CIFC25 H41 N3 O5 Si2P 1 21/c 110.7784; 30.335; 10.6785
90; 115.168; 90
3160Liu, Yang; Jin, Shiyu; Wang, Zi; Song, Linhua; Hu, Youhong
Microwave Assisted Tandem Heck-Sonogashira Reactions of N,N-Di-Boc-Protected 6-Amino-5-iodo-2-methyl Pyrimidin-4-ol in An Efficient Approach to Functionalized Pyrido[2,3-d]Pyrimidines.
Organic letters, 2014, 16, 3524-3527
1516707 CIFC30 H21 NP -111.0471; 12.0602; 16.587
79.775; 77.726; 86.565
2124.5Wang, Shaoyin; Chai, Zhuo; Wei, Yun; Zhu, Xiancui; Zhou, Shuangliu; Wang, Shaowu
Lewis Acid Catalyzed Cascade Reaction to Carbazoles and Naphthalenes via Dehydrative [3 + 3]-Annulation.
Organic letters, 2014, 16, 3592-3595
1516708 CIFC31 H23 N OP -110.6667; 12.2374; 18.702
73.907; 82.088; 76.905
2277.2Wang, Shaoyin; Chai, Zhuo; Wei, Yun; Zhu, Xiancui; Zhou, Shuangliu; Wang, Shaowu
Lewis Acid Catalyzed Cascade Reaction to Carbazoles and Naphthalenes via Dehydrative [3 + 3]-Annulation.
Organic letters, 2014, 16, 3592-3595
1516709 CIFC30 H22 O2P n a 217.5251; 13.3225; 21.8161
90; 90; 90
2187.1Wang, Shaoyin; Chai, Zhuo; Wei, Yun; Zhu, Xiancui; Zhou, Shuangliu; Wang, Shaowu
Lewis Acid Catalyzed Cascade Reaction to Carbazoles and Naphthalenes via Dehydrative [3 + 3]-Annulation.
Organic letters, 2014, 16, 3592-3595
1516710 CIFC23 H16 O4P -16.737; 10.853; 12.232
80.759; 86.793; 73.199
845Bhojgude, Sachin Suresh; Thangaraj, Manikandan; Suresh, Eringathodi; Biju, Akkattu T.
Tandem [4 + 2]/[2 + 2] cycloaddition reactions involving indene or benzofurans and arynes.
Organic letters, 2014, 16, 3576-3579
1516711 CIFC24 H22 OP n a 217.9519; 12.792; 17.476
90; 90; 90
1777.7Bhojgude, Sachin Suresh; Thangaraj, Manikandan; Suresh, Eringathodi; Biju, Akkattu T.
Tandem [4 + 2]/[2 + 2] cycloaddition reactions involving indene or benzofurans and arynes.
Organic letters, 2014, 16, 3576-3579
1516712 CIFC28 H27 N O3 SP 1 21/n 112.055; 8.557; 23.454
90; 90.843; 90
2419.1Feng, Xin; Wang, Huiqing; Yang, Bo; Fan, Renhua
One-Pot Synthesis of Highly Substituted 4-Acetonylindoles via Sequential Dearomatization and Silver-Catalyzed Domino Reaction.
Organic letters, 2014, 16, 3600-3603
1516713 CIFC21 H22 N2 O6P 1 21/c 18.762; 27.035; 8.561
90; 99.436; 90
2000.5Li, Deng Yuan; Mao, Xiao Feng; Chen, Hao Jie; Chen, Guo Rong; Liu, Pei Nian
Rhodium-Catalyzed Addition-Cyclization of Hydrazines with Alkynes: Pyrazole Synthesis via Unexpected C-N Bond Cleavage.
Organic letters, 2014, 16, 3476-3479
1516714 CIFC19 H15 Cl N2 O4P -18.9238; 10.559; 11.636
63.623; 88.104; 66.937
890.5Li, Deng Yuan; Mao, Xiao Feng; Chen, Hao Jie; Chen, Guo Rong; Liu, Pei Nian
Rhodium-Catalyzed Addition-Cyclization of Hydrazines with Alkynes: Pyrazole Synthesis via Unexpected C-N Bond Cleavage.
Organic letters, 2014, 16, 3476-3479
1516715 CIFC21 H22 N2 O6P -19.0549; 10.608; 11.805
71.659; 87.306; 73.948
1033.4Li, Deng Yuan; Mao, Xiao Feng; Chen, Hao Jie; Chen, Guo Rong; Liu, Pei Nian
Rhodium-Catalyzed Addition-Cyclization of Hydrazines with Alkynes: Pyrazole Synthesis via Unexpected C-N Bond Cleavage.
Organic letters, 2014, 16, 3476-3479
1516726 CIFC26 H23 N O2P 21 21 219.115; 10.756; 19.937
90; 90; 90
1954.6Marsh, Barrie J.; Adams, Harry; Barker, Mike D.; Kutama, Ibrahim U.; Jones, Simon
Enantioselective Catalytic Desymmetrization of Maleimides by Temporary Removal of an Internal Mirror Plane and Stereoablative Over-reduction: Synthesis of (R)-Pyrrolam A.
Organic letters, 2014, 16, 3780
1516727 CIFC26 H23 N O3P 21 21 218.755; 11.955; 19.235
90; 90; 90
2013.3Marsh, Barrie J.; Adams, Harry; Barker, Mike D.; Kutama, Ibrahim U.; Jones, Simon
Enantioselective Catalytic Desymmetrization of Maleimides by Temporary Removal of an Internal Mirror Plane and Stereoablative Over-reduction: Synthesis of (R)-Pyrrolam A.
Organic letters, 2014, 16, 3780
1516742 CIFC27 H33 F O8C 1 2 138.884; 8.6698; 7.8123
90; 92.945; 90
2630.2Morton, Gillian E.; Barrett, Anthony G. M.
Iterative benzyne-furan cycloaddition reactions: studies toward the total synthesis of ent-Sch 47554 and ent-Sch 47555.
Organic letters, 2006, 8, 2859-2861
1516743 CIFC39 H36 N3 O PP 21 21 2110.6365; 16.1655; 18.138
90; 90; 90
3118.7Fekner, Tomasz; Müller-Bunz, Helge; Guiry, Patrick J.
Synthesis and application of quinazoline-oxazoline-containing (quinazox) ligands.
Organic letters, 2006, 8, 5109-5112
1516744 CIFC40 H38 N3 O PP 21 21 2110.9951; 16.296; 18.095
90; 90; 90
3242.2Fekner, Tomasz; Müller-Bunz, Helge; Guiry, Patrick J.
Synthesis and application of quinazoline-oxazoline-containing (quinazox) ligands.
Organic letters, 2006, 8, 5109-5112
1516745 CIFC38 H42 O2 Si2P 1 21/c 119.596; 7.5959; 12.4831
90; 107.84; 90
1768.8Liu, Yuanhong; Gao, Hongjun
New zirconium-mediated approach toward regio- and stereocontrolled synthesis of trans-enediynes.
Organic letters, 2006, 8, 309-311
1516746 CIFC24 H18 B N O3P b c a14.8638; 15.4624; 16.3768
90; 90; 90
3763.9Yasuda, Makoto; Yoshioka, Sachiko; Yamasaki, Satoshi; Somyo, Toshio; Chiba, Kouji; Baba, Akio
Cage-shaped borate esters with enhanced Lewis acidity and catalytic activity.
Organic letters, 2006, 8, 761-764
1516747 CIFC3 H8 N6C 1 2/c 113.574; 4.9473; 36.772
90; 96.297; 90
2454.5Tominey, Alan F.; Docherty, Paul H.; Rosair, Georgina M.; Quenardelle, Romain; Kraft, Arno
Unusually weak binding interactions in tetrazole-amidine complexes.
Organic letters, 2006, 8, 1279-1282
1516748 CIFC8 H10 N6P 1 21/c 17.2044; 8.5549; 15.472
90; 99.564; 90
940.3Tominey, Alan F.; Docherty, Paul H.; Rosair, Georgina M.; Quenardelle, Romain; Kraft, Arno
Unusually weak binding interactions in tetrazole-amidine complexes.
Organic letters, 2006, 8, 1279-1282
1516749 CIFC3 H8 N2 O2P 43 21 26.4456; 6.4456; 12.53
90; 90; 90
520.57Tominey, Alan F.; Docherty, Paul H.; Rosair, Georgina M.; Quenardelle, Romain; Kraft, Arno
Unusually weak binding interactions in tetrazole-amidine complexes.
Organic letters, 2006, 8, 1279-1282

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