Pure and Applied Chemistry

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• Suzuki Takahiro, Okuyama Hiroshi, Takano Atsuhiro, Suzuki Shinya, Shimizu Isao, Kobayashi Susumu: Synthesis of Dibarrelane, a Dibicyclo[2.2.2]octane Hydrocarbon. J. Org. Chem. 2014, 140303082206003. <http://dx.doi.org/10.1021/jo5003455>
• Kobayakawa Yu, Nakada Masahisa: Total Syntheses of (−)-Scabronines G and A, and (−)-Episcabronine A. Angew. Chem. 2013, 125, 7717. <http://dx.doi.org/10.1002/ange.201303224>
• Bao Xu, Cao Ye-Xing, Chu Wen-Dao, Qu Hu, Du Ji-Yuan, Zhao Xian-He, Ma Xiao-Yan, Wang Cheng-Tao, Fan Chun-An: Bioinspired Total Synthesis of Montanine-Type Amaryllidaceae Alkaloids. Angew. Chem. 2013, 125, 14417. <http://dx.doi.org/10.1002/ange.201307324>
• Kobayakawa Yu, Nakada Masahisa: Total Syntheses of (−)-Scabronines G and A, and (−)-Episcabronine A. Angew. Chem. Int. Ed. 2013, 52, 7569. <http://dx.doi.org/10.1002/anie.201303224>
• Bao Xu, Cao Ye-Xing, Chu Wen-Dao, Qu Hu, Du Ji-Yuan, Zhao Xian-He, Ma Xiao-Yan, Wang Cheng-Tao, Fan Chun-An: Bioinspired Total Synthesis of Montanine-Type Amaryllidaceae Alkaloids. Angew. Chem. Int. Ed. 2013, 52, 14167. <http://dx.doi.org/10.1002/anie.201307324>
• Chittimalla Santhosh Kumar, Kuppusamy Rajesh, Thiyagarajan Kamalraj, Bandi Chennakesavulu: Reaction of Nitrile Oxides with Masked o -Benzoquinones; Synthesis of Highly Functionalized Isoxazolines. Eur. J. Org. Chem. 2013, 2013, 2715. <http://dx.doi.org/10.1002/ejoc.201201670>
• Deslongchamps Ghislain, Deslongchamps Pierre: Bent bonds and the antiperiplanar hypothesis as a simple model to predict Diels–Alder reactivity: retrospective or perspective?. Tetrahedron 2013, 69, 6022. <http://dx.doi.org/10.1016/j.tet.2013.05.008>
• Singh Vishwakarma, Islam Sk. Nurul, Mali Jyotirling: Molecular diversity from aromatics. A tandem oxidative dearomatization, cycloaddition and reactivity modulation in excited states: synthesis of tricyclo[5.3.1.01,5]undecanes and bicyclo[4.2.0]octanes from common precursors. Tetrahedron 2013, 69, 8865. <http://dx.doi.org/10.1016/j.tet.2013.08.015>
• Tsao Kuo-Wei, Devendar Badugu, Liao Chun-Chen: Ring rearrangement metathesis of 2-allylbicyclo[2.2.2]octenes: a short entry to cis-hydrindenols from 2-methoxyphenols. Tetrahedron Letters 2013, 54, 3055. <http://dx.doi.org/10.1016/j.tetlet.2013.03.142>
• Gao Jihong, Orso Simon Josephine, Rodrigo Russell, Assoud Abdeljalil: From Chiral ortho-Benzoquinone Monoketals to Nonracemic Indolinocodeines through Diels–Alder and Cope Reactions. J. Org. Chem. 2013, 78, 48. <http://dx.doi.org/10.1021/jo3014098>
• Liu Ling, Li Yan, Li Li, Cao Ya, Guo Liangdong, Liu Gang, Che Yongsheng: Spiroketals of Pestalotiopsis fici Provide Evidence for a Biosynthetic Hypothesis Involving Diversified Diels–Alder Reaction Cascades. J. Org. Chem. 2013, 78, 2992. <http://dx.doi.org/10.1021/jo302804h>
• Shen Shou-Jie, Li Wei-Dong Z.: Formal Homoiodo Allylsilane Annulations: Dual Total Syntheses of (±)-Hirsutene and (±)-Capnellene. J. Org. Chem. 2013, 78, 7112. <http://dx.doi.org/10.1021/jo4009854>
• Chou Yu-Yu, Liao Chun-Chen: First Asymmetric Total Syntheses and Determination of Absolute Configurations of (+)-Eudesmadiene-12,6-olide and (+)-Frullanolide. Org. Lett. 2013, 15, 1584. <http://dx.doi.org/10.1021/ol4003724>
• Suzuki Takahiro, Miyajima Yuria, Suzuki Kaname, Iwakiri Kanako, Koshimizu Masaki, Hirai Go, Sodeoka Mikiko, Kobayashi Susumu: Unexpected Diels–Alder/Carbonyl-ene Cascade toward the Biomimetic Synthesis of Chloropupukeananin. Org. Lett. 2013, 15, 1748. <http://dx.doi.org/10.1021/ol400549q>
• Reddy Parumala Santosh Kumar, Peddinti Rama Krishna: Reversal of Polarity in Masked o-Benzoquinones: Rapid Access to Unsymmetrical Oxygenated Biaryls. Org. Lett. 2013, 15, 3546. <http://dx.doi.org/10.1021/ol401341s>
• Murphy Rebecca A., Sarpong Richmond: Direct Methoxypyridine Functionalization Approach to Magellanine-Type Lycopodium Alkaloids. Org Lett 2012, 14, 632. <http://dx.doi.org/10.1021/ol203269f>
• Zhang Guo-Biao, Wang Fang-Xin, Du Ji-Yuan, Qu Hu, Ma Xiao-Yan, Wei Meng-Xue, Wang Cheng-Tao, Li Qiong, Fan Chun-An: Toward the Total Synthesis of Palhinine A: Expedient Assembly of Multifunctionalized Isotwistane Ring System with Contiguous Quaternary Stereocenters. Org. Lett. 2012, 14, 3696. <http://dx.doi.org/10.1021/ol301534r>
• Roche Stéphane P., Porco John A.: Desaromatisierungsstrategien in der Synthese strukturell komplexer Naturstoffe. Angew Chem 2011, 123, 4154. <http://dx.doi.org/10.1002/ange.201006017>
• Suzuki Takahiro, Sasaki Aya, Egashira Naoki, Kobayashi Susumu: A Synthetic Study of Atropurpuran: Construction of a Pentacyclic Framework by an Intramolecular Reverse-Electron-Demand Diels-Alder Reaction. angew chemie 2011, 123, 9343. <http://dx.doi.org/10.1002/ange.201103950>
• Roche Stéphane P., Porco John A.: Dearomatization Strategies in the Synthesis of Complex Natural Products. Angew Chem Int Ed 2011, 50, 4068. <http://dx.doi.org/10.1002/anie.201006017>
• Suzuki Takahiro, Sasaki Aya, Egashira Naoki, Kobayashi Susumu: A Synthetic Study of Atropurpuran: Construction of a Pentacyclic Framework by an Intramolecular Reverse-Electron-Demand Diels-Alder Reaction. Angew Chem Int E 2011, 50, 9177. <http://dx.doi.org/10.1002/anie.201103950>
• Snyder Scott A., Kontes Ferenc: Synthetic Studies of Biomimetic Diels-Alder Processes toward the Helicterin Family of Natural Products. Isr J Chem 2011, 51, 378. <http://dx.doi.org/10.1002/ijch.201100004>
• Yu Min, Snider Barry B.: Diels–Alder reaction of maldoxin with an isopropenylallene. Tedrahedron 2011, 67, 9473. <http://dx.doi.org/10.1016/j.tet.2011.09.117>
• Surasani Seshi Reddy, Peddinti Rama Krishna: Diels–Alder reaction of 4-halogenated masked o-benzoquinones with electron-rich dienophiles. Tetrahetron Lett 2011, 52, 4615. <http://dx.doi.org/10.1016/j.tetlet.2011.06.086>
• Chen Lei, Hua Zhengmao, Li Gangqin, Jin Zhendong: Controlling the Facial Selectivity of Asymmetric [4 + 2] Cyclo-additions: A Concise Synthesis of the cis-Decalin Core Structure of Superstolides A and B. Org. Lett. 2011, 13, 3580. <http://dx.doi.org/10.1021/ol201095b>
• Chou Yu-Yu, Tung Yen-Shih, Liao Chun-Chen, Hsu Day-Shin: Photochemistry of Tricyclo[5.2.2.0^2,6]undeca-4,10-dien-8-ones: An Efficient General Route to Substituted Linear Triquinanes from 2-Methoxyphenols. Total Synthesis of (±)-Δ⁹⁽¹²⁾-Capnellene. Chem Eur J 2010, 16, 3121. <http://dx.doi.org/10.1002/chem.200902752>
• Pouységu Laurent, Deffieux Denis, Quideau Stéphane: Hypervalent iodine-mediated phenol dearomatization in natural product synthesis. Tetrahedron 2010, 66, 2235. <http://dx.doi.org/10.1016/j.tet.2009.12.046>
• Surasani Seshi Reddy, Rajora Virendra Singh, Bodipati Naganjaneyulu, Peddinti Rama Krishna: Diels–Alder reactions of halogenated masked o-benzoquinones: synthesis of halogen-substituted bicyclo[2.2.2]octenones. Tetrahetron Lett 2009, 50, 773. <http://dx.doi.org/10.1016/j.tetlet.2008.11.117>
• Chang Chun-Ping, Chen Ching-Hsien, Chuang Gary Jing, Liao Chun-Chen: Cyclopropane ring-opening of tricyclo[3.3.0.02,8]octan-3-ones: a quick access to bicyclo[3.2.1]octanones from 2-methoxyphenols. Tetrahetron Lett 2009, 50, 3414. <http://dx.doi.org/10.1016/j.tetlet.2009.02.150>
• Kao Tzu-Chiao, Chuang Gary Jing, Liao Chun-Chen: Photooxygenation of Masked o-Benzoquinones: An Efficient Entry into Highly Functionalized Cyclopentenones from 2-Methoxyphenols. Angew Chem 2008, 120, 7435. <http://dx.doi.org/10.1002/ange.200802130>
• Luo Shun-Yuan, Jang Yeong-Jiunn, Liu Jing-Yuan, Chu Chrong-Shyua, Liao Chun-Chen, Hung Shang-Cheng: Carbohydrate-Templated Asymmetric Diels-Alder Reactions of Masked ortho-Benzoquinones for the Synthesis of Chiral Bicyclo[2.2.2]oct-5-en-2-ones. Angew Chem 2008, 120, 8202. <http://dx.doi.org/10.1002/ange.200802693>
• Kao Tzu-Chiao, Chuang Gary Jing, Liao Chun-Chen: Photooxygenation of Masked o-Benzoquinones: An Efficient Entry into Highly Functionalized Cyclopentenones from 2-Methoxyphenols. Angew Chem Int Ed 2008, 47, 7325. <http://dx.doi.org/10.1002/anie.200802130>
• Luo Shun-Yuan, Jang Yeong-Jiunn, Liu Jing-Yuan, Chu Chrong-Shyua, Liao Chun-Chen, Hung Shang-Cheng: Carbohydrate-Templated Asymmetric Diels-Alder Reactions of Masked ortho-Benzoquinones for the Synthesis of Chiral Bicyclo[2.2.2]oct-5-en-2-ones. Angew Chem Int Ed 2008, 47, 8082. <http://dx.doi.org/10.1002/anie.200802693>
• Lu Yan-Bin, Lee Tsung-Ho, Liu Wen-Cheng, Chuang Gary Jing, Liao Chun-Chen: 1,3- and 1,2-Carbo-Migration of 2-Vinylbicyclo[2.2.2]octenols: Facile and Concise Synthesis of Bicyclo[4.2.2]/[3.2.2] Skeleton by Two/One-Carbon Ring Expansion. Chem Asian J 2008, 3, 1422. <http://dx.doi.org/10.1002/asia.200800113>
• Banwell Martin G., Austin Kerrie A.B., Willis Anthony C.: Chemoenzymatic total syntheses of the linear triquinane-type natural products (+)-hirsutic acid and (−)-complicatic acid from toluene. Tetrahedron 2007, 63, 6388. <http://dx.doi.org/10.1016/j.tet.2007.03.073>
• Austin Kerrie A.B., Banwell Martin G., Harfoot Gwion J., Willis Anthony C.: Chemoenzymatic syntheses of the linear triquinane-type sesquiterpenes (+)-hirsutic acid and (−)-complicatic acid. Tetrahetron Lett 2006, 47, 7381. <http://dx.doi.org/10.1016/j.tetlet.2006.07.145>
• Chittimalla Santhosh Kumar, Shiao Hui-Yi, Liao Chun-Chen: Domino retro Diels?Alder/Diels?Alder reaction: an efficient protocol for the synthesis of highly functionalized bicyclo[2.2.2]octenones and bicyclo[2.2.2]octadienones. Org Biomol Chem 2006, 4, 2267. <http://dx.doi.org/10.1039/b602928k>
• Liao Chun-Chen: Masked O-Benzoquinone Strategy in Organic Synthesis: Short and Efficient Construction of cis-Decalins and Linear Triquinanes from 2-Methoxyphenols. ChemInform 2005, 36. <http://dx.doi.org/10.1002/chin.200550264>