Pure and Applied Chemistry

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• Kumar N. V. Suresh, Priyakumar U. Deva, Singh Harjinder, Roy Saumya, Chakraborty Tushar Kanti: Inter- versus intra-molecular cyclization of tripeptides containing tetrahydrofuran amino acids: a density functional theory study on kinetic control. J Mol Model 2012, 18, 3181. <http://dx.doi.org/10.1007/s00894-011-1326-7>
• Yadav J.S., Nagendra Reddy C., Sabitha G.: Synthesis of the C38�C54 spiroketal segment of halichondrin B. Tetrahedron Letters 2012, 53, 2504. <http://dx.doi.org/10.1016/j.tetlet.2012.02.090>
• Ferreira Sabrina Baptista, Kaiser Carlos Roland: Pyrazine derivatives: a patent review (2008 – present). Expert Opin. Ther. Patents 2012, 22, 1033. <http://dx.doi.org/10.1517/13543776.2012.714370>
• Shawakfeh Khaled Q., Al-Said Naim H.: Synthesis of new symmetrical bis-steroidal pyrazine analogues from diosgenin. Steroid 2011, 76, 232. <http://dx.doi.org/10.1016/j.steroids.2010.10.002>
• PETTIT G. R.: ChemInform Abstract: Marine Animal and Terrestral Plant Anticancer Constituents. ChemInform 2010, 26, no. <http://dx.doi.org/10.1002/chin.199508296>
• Kumar N. V. Suresh, Sharma Purshotam, Singh Harjinder, Koley Dipankar, Roy Saumya, Chakraborty Tushar Kanti: Preferential mode of cyclization of tetrahydrofuran amino acids containing peptides: some theoretical insights. J Phys Org Chem 2009, n/a. <http://dx.doi.org/10.1002/poc.1609>
• Braun Alain, Cho Il Hwan, Ciblat Stephane, Clyne Dean, Forgione Pat, Hart Amy C., Huang Guoxiang, Kim Jungchul, Modolo Isabelle, Paquette Leo A.: Enantioselective synthesis of structurally intricate and complementary polyoxygenated building blocks of Spongistatin 1 (Altohyrtin A). Collect Czech Chem Commun 2009, 1. <http://dx.doi.org/10.1135/cccc2008181>
• Wang Rong-Min, He Nai-Pu, Song Peng-Fei, He Yu-Feng, Ding Lan, Lei Ziqiang: Preparation of low-molecular-weight chitosan derivative zinc complexes and their effect on the growth of liver cancer cells in vitro. Pure and App Chemis 2009, 1. <http://dx.doi.org/10.1351/PAC-CON-08-11-15>
• Smith, III Amos B., Wuest William M.: Evolution of multi-component anion relay chemistry (ARC): construction of architecturally complex natural and unnatural products. Chem Commun 2008, 5883. <http://dx.doi.org/10.1039/b810394a>
• Kumar Pradeep, Naidu Vasudeva, Gupta Priti: Application of hydrolytic kinetic resolution (HKR) in the synthesis of bioactive compounds. Tetrahedron 2007, 63, 2745. <http://dx.doi.org/10.1016/j.tet.2006.12.015>
• Wang Zhiyong, McPherson Peter A., Raccor Brianne S., Balachandran Raghavan, Zhu Guangyu, Day Billy W., Vogt Andreas, Wipf Peter: Structure?activity and High-content Imaging Analyses of Novel Tubulysins. Chem Biol Drug Design 2007, 70, 75. <http://dx.doi.org/10.1111/j.1747-0285.2007.00541.x>
• Yeh Vince S.C.: Recent advances in the total syntheses of oxazole-containing natural products. Tetrahedron 2004, 60, 11995. <http://dx.doi.org/10.1016/j.tet.2004.10.001>
• Wipf Peter, Takada Takeshi, Rishel Michael J.: Synthesis of the Tubuvaline-Tubuphenylalanine (Tuv-Tup) Fragment of Tubulysin. Org Lett 2004, 6, 4057. <http://dx.doi.org/10.1021/ol048252i>
• Smith Amos B., Sfouggatakis Chris, Gotchev Dimitar B., Shirakami Shohei, Bauer David, Zhu Wenyu, Doughty Victoria A.: Spongistatin Synthetic Studies. Evolution of a Scalable Synthesis for the EF Fragment of (+)-Spongistatin 1 Exploiting a Petasis−Ferrier Union/Rearrangement Tactic. Org Lett 2004, 6, 3637. <http://dx.doi.org/10.1021/ol048418f>
• Ceide S. C., Trembleau L., Haberhauer G., Somogyi L., Lu X., Bartfai T., Rebek J.: Synthesis of galmic: A nonpeptide galanin receptor agonist. Proceedings of the National Academy of Sciences 2004, 101, 16727. <http://dx.doi.org/10.1073/pnas.0407543101>
• Smith Amos B., Zhu Wenyu, Shirakami Shohei, Sfouggatakis Chris, Doughty Victoria A., Bennett Clay S., Sakamoto Yasuharu: Total Synthesis of (+)-Spongistatin 1. An Effective Second-Generation Construction of an Advanced EF Wittig Salt, Fragment Union, and Final Elaboration. Org Lett 2003, 5, 761. <http://dx.doi.org/10.1021/ol034037a>
• Austad Brian C, Hart Amy C, Burke Steven D: Halichondrin B: synthesis of the C(37)–C(54) subunit. Tetrahedron 2002, 58, 2011. <http://dx.doi.org/10.1016/S0040-4020(02)00050-9>
• Haberhauer Gebhard, Rominger Frank: Synthesis of a new class of imidazole-based cyclic peptides. Tetrahetron Lett 2002, 43, 6335. <http://dx.doi.org/10.1016/S0040-4039(02)01365-5>
• Smith Amos B., Doughty Victoria A., Sfouggatakis Chris, Bennett Clay S., Koyanagi Jyunichi, Takeuchi Makoto: Spongistatin Synthetic Studies. An Efficient, Second-Generation Construction of an Advanced ABCD Intermediate. Org Lett 2002, 4, 783. <http://dx.doi.org/10.1021/ol017273z>
• Smith III Amos B., Doughty Victoria A., Lin Qiyan, Zhuang Linghang, McBriar Mark D., Boldi Armen M., Moser William H., Murase Noriaki, Nakayama Kiyoshi, Sobukawa Masao: The Spongistatins: Architecturally Complex Natural Products—Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment. Angew Chem 2001, 113, 197. <http://dx.doi.org/10.1002/1521-3757(20010105)113:1<197::AID-ANGE197>3.0.CO;2-7>
• Smith III Amos B., Lin Qiyan, Doughty Victoria A., Zhuang Linghang, McBriar Mark D., Kerns Jeffrey K., Brook Christopher S., Murase Noriaki, Nakayama Kiyoshi: The Spongistatins: Architecturally Complex Natural Products—Part Two: Synthesis of the C(29–51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2. Angew Chem 2001, 113, 202. <http://dx.doi.org/10.1002/1521-3757(20010105)113:1<202::AID-ANGE202>3.0.CO;2-M>
• Doughty Victoria A., Lin Qiyan, Zhuang Linghang, McBriar Mark D., Smith III Amos B., Boldi Armen M., Moser William H., Murase Noriaki, Nakayama Kiyoshi, Sobukawa Masao: The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment. Angewandte Chemie-Int Ed 2001, 40, 191. <http://dx.doi.org/10.1002/1521-3773(20010105)40:1<191::AID-ANIE191>3.0.CO;2-C>
• Smith III Amos B., Lin Qiyan, Doughty Victoria A., Zhuang Linghang, McBriar Mark D., Kerns Jeffrey K., Brook Christopher S., Murase Noriaki, Nakayama Kiyoshi: The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2. Angewandte Chemie-Int Ed 2001, 40, 196. <http://dx.doi.org/10.1002/1521-3773(20010105)40:1<196::AID-ANIE196>3.0.CO;2-T>
• Somogyi László, Haberhauer Gebhard, Rebek Julius: Improved synthesis of functionalized molecular platforms related to marine cyclopeptides. Tetrahedron 2001, 57, 1699. <http://dx.doi.org/10.1016/S0040-4020(00)01173-X>
• Zuev Dmitry, Paquette Leo A.: A Modular Approach to Marine Macrolide Construction. 3. Enantioselective Synthesis of the C1−C28 Sector of Spongistatin 1 (Altohyrtin A). Org Lett 2000, 2, 679. <http://dx.doi.org/10.1021/ol0000049>
• Lee Mike S., Kerns Edward H.: LC/MS applications in drug development. Mass Spectrom Rev 1999, 18, 187. <http://dx.doi.org/10.1002/(SICI)1098-2787(1999)18:3/4<187::AID-MAS2>3.0.CO;2-K>
• Guo Chuangxing, Ma Sunghoon, Jeong Jae Uk, Boyd Michael R., Matsunaga Shikegi, Fusetani Nobuhiro, Fuchs P.L., LaCour Thomas G.: On topography and functionality in the B-D rings of cephalostatin cytotoxins. Bioog Med Chem Lett 1999, 9, 2587. <http://dx.doi.org/10.1016/S0960-894X(99)00430-8>
• Guo Jiasheng, Duffy Kevin J., Stevens Kirk L., Dalko Peter I., Roth Rebecca M., Hayward Matthew M., Kishi Yoshito: Totalsynthese von Altohyrtin A (Spongistatin 1): Teil 1. Angew Chem 1998, 110, 198. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980116)110:1/2<198::AID-ANGE198>3.0.CO;2-0>
• Nicolaou Kyriacos C., Roschangar Frank, Vourloumis Dionisios: Chemie und Biologie der Epothilone. Angew Chem 1998, 110, 2120. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980803)110:15<2120::AID-ANGE2120>3.0.CO;2-5>
• Pietruszka Jörg: Spongistatine, Cynachyrolide oder Altohyrtine? Marine Makrolide in der Krebsforschung. Angew Chem 1998, 110, 2773. <http://dx.doi.org/10.1002/(SICI)1521-3757(19981002)110:19<2773::AID-ANGE2773>3.0.CO;2-0>
• Lemaire-Audoire Sandrine, Vogel Pierre: Total synthesis of the C37C45 F-ring fragment of spongistatins. Tetrahetron Lett 1998, 39, 1345. <http://dx.doi.org/10.1016/S0040-4039(97)10817-6>
• Terauchi Takeshi, Nakata Masaya: Synthetic studies on altohyrtins (spongistatins): Synthesis of the C1C14 (AB) spiroacetal portion. Tetrahetron Lett 1998, 39, 3795. <http://dx.doi.org/10.1016/S0040-4039(98)00619-4>
• Paterson Ian, Wallace Debra J., Oballa Renata M.: Studies in marine macrolide synthesis: Synthesis of a fully functionalised C1C28 subunit of spongistatin 1 (altohyrtin A). Tetrahetron Lett 1998, 39, 8545. <http://dx.doi.org/10.1016/S0040-4039(98)01908-X>
• Pettit Robin K, McAllister Shane C, Pettit George R, Herald Cherry L, Johnson J.Morris, Cichacz Zbigniew A: A broad-spectrum antifungal from the marine sponge Hyrtios erecta. Intl J Antimicrob Agents 1998, 9, 147. <http://dx.doi.org/10.1016/S0924-8579(97)00044-7>
• Smith Amos B, Lin Qiyan, Pettit George R, Chapuis Jean-Charles, Schmidt Jean M: Synthesis and in vitro cancer cell growth inhibitory activity of monocyclic model compounds containing spongistatin triene side-chains. Biorg Med Chem Lett 1998, 8, 567. <http://dx.doi.org/10.1016/S0960-894X(98)00050-X>
• Dunkel Ralf, Mentzel Matthias, Hoffmann H.M.R.: 8-oxabicyclo[3.2.1]oct-6-en-3-one as a module for the synthesis of β-alkoxy-δ-valerolactones relevant to natural products and drugs. Tetrahedron 1997, 53, 14929. <http://dx.doi.org/10.1016/S0040-4020(97)10025-4>
• Paquette Leo A., Zuev Dmitry: A modular approach to marine macrolide construction. 1. An enantiocontrolled route to the C1–C12 (AB) spiroacetal sector. Tetrahetron Lett 1997, 38, 5115. <http://dx.doi.org/10.1016/S0040-4039(97)01140-4>
• Paquette Leo A., Braun Alain: A modular approach to marine macrolide construction. 2. Concise stereocontrolled synthesis of the C17–C28 (CD) spiroacetal component. Tetrahetron Lett 1997, 38, 5119. <http://dx.doi.org/10.1016/S0040-4039(97)01141-6>
• Paterson Ian, Keown Linda E: Studies in marine macrolide synthesis: Stereocontrolled synthesis of the F-ring subunit of spongistatin 1 (altohyrtin A). Tetrahetron Lett 1997, 38, 5727. <http://dx.doi.org/10.1016/S0040-4039(97)01257-4>
• Paterson Ian, Oballa Renata M.: Studies in marine macrolide synthesis: Synthesis of the C1C15 subunit of spongistatin 1 (altohyrtin A) and 15,16-anti aldol coupling reactions. Tetrahetron Lett 1997, 38, 8241. <http://dx.doi.org/10.1016/S0040-4039(97)10126-5>
• Paterson Ian, Wallace Debra J, Gibson Karl R: Studies in marine macrolide synthesis: Synthesis of a C16C28 subunit of spongistatin 1 (altohyrtin A) incorporating the CD-spiroacetal moiety. Tetrahetron Lett 1997, 38, 8911. <http://dx.doi.org/10.1016/S0040-4039(97)10483-X>
• Smith Amos B., Zhuang Linghang, Brook Christopher S., Boldi Armen M., McBriar Mark D., Moser William H., Murase Noriaki, Nakayama Kiyoshi, Verhoest Patrick R., Lin Qiyan: Spongistatin synthetic studies. 1. Construction of a C(29–48) subtarget. Tetrahetron Lett 1997, 38, 8667. <http://dx.doi.org/10.1016/S0040-4039(97)10499-3>
• Nisbet Louis J, Moore Michael: Will natural products remain an important source of drug research for the future?. curr opin biotechnol 1997, 8, 708. <http://dx.doi.org/10.1016/S0958-1669(97)80124-3>
• Gauthier Donald R., Carreira Erick M.: Katalytische, enantioselektive Addition von Allylsilanen an Aldehyde: Bildung eines neuartigen reaktiven TiIV-Komplexes aus TiF4. Angew Chem 1996, 108, 2521. <http://dx.doi.org/10.1002/ange.19961082018>
• Paterson Ian, Oballa Renata M., Norcross Roger D.: Studies in marine macrolide synthesis: Stereocontrolled synthesis of the AB-spiroacetal subunit of spongistatin 1 (altohyrtin A). Tetrahetron Lett 1996, 37, 8581. <http://dx.doi.org/10.1016/0040-4039(96)01961-2>