Crystallography Open Database

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Searching journal of publication like 'Organic letters' volume of publication is 14

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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; DobrzaƄska, 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

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