Synthesis

Issue 12 · June 2017

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review
2589
Gettys, Kristen E.; Ye, Zhishi; Dai, Mingji: Recent Advances in Piperazine Synthesis

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2605
Glinsky-Olivier, Nicolas; Guinchard, Xavier: Enantioselective Catalytic Methods for the Elaboration of Chiral Tetrahydro-β-carbolines and Related Scaffolds

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2621
Naidoo, Shivani; Jeena, Vineet: Synthesis of 2,4-Disubstituted Quinoline Derivatives via A³-Coupling: An EcoScale Evaluation

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2632
Heindl, Andreas H.; Schweighauser, Luca; Logemann, Christian; Wegner, Hermann A.: Azobenzene Macrocycles: Synthesis of a Z-Stable Azobenzenophane

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2640
Afanasyev, Oleg I.; Tsygankov, Alexey A.; Usanov, Dmitry L.; Perekalin, Dmitry S.; Samoylova, Alexandra D.; Chusov, Denis: Some Aspects of Reductive Amination in the Presence of Carbon Monoxide: Cyclopropyl Ketones as Bifunctional Electrophiles

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2652
Ledingham, Edward T.; Merritt, Christopher J.; Sumby, Christopher J.; Taylor, Michelle K.; Greatrex, Ben W.: Stereoselective Cyclopropanation of (–)-Levoglucosenone Derivatives Using Sulfonium and Sulfoxonium Ylides

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2663
Motevalli, Somayeh; Johnson, Jeffrey S.: Phosphite-Mediated Reductive Cross-Coupling of Isatins and Nitrostyrenes

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2677
da Silveira Pinto, Ligia S.; de Souza, Marcus V. N.: Sonochemistry as a General Procedure for the Synthesis of Coumarins, Including Multigram Synthesis

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2683
De Munck, Lode; Vila, Carlos; Pons, Carolina; Pedro, José R.: Synthesis of Multisubstituted 1,4-Dihydrobenzoxazin-2-ones through a One-Pot Nucleophilic N-Alkylation/C-Alkylation of Cyclic α-Imino Esters

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2691
Schneider, Tobias; Martin, Joshua; Durkin, Patrick M.; Kubyshkin, Vladimir; Budisa, Nediljko: The Regioselective Synthesis of o-Nitrobenzyl DOPA Derivatives

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2700
Singh, Prabal P.; Yugandar, S.; Kumar, S. Vijay; Ila, H.; Junjappa, H.: Synthesis of Novel Five- and Six-Membered Ferrocene-Containing Heterocycles and Heteroaromatics via Cyclocondensation of 1-Ferrocenyl-3,3-bis(methylthio)prop-2-en-1-one with Various Bifunctional Nucleophiles

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2711
Li, Hongji; Deng, Hong: A Highly Selective Amidation of Azoxybenzenes with Sulfonamides via Rhodium(III)-Catalyzed C–H Activation

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2721
Sang, Dayong; Wang, Jiahui; Zheng, Yun; He, Jianyuan; Yuan, Caili; An, Qing; Tian, Juan: Carbodiimides as Acid Scavengers in Aluminum Triiodide Induced Cleavage of Alkyl Aryl Ethers

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2727
Feng, Xiujuan; Zhang, Haixia; Lu, Wenbo; Yamamoto, Yoshinori; Almansour, Abdulrahman I.; Arumugam, Natarajan; Kumar, Raju Suresh; Bao, Ming: Stereoselective Synthesis of Vinyl Iodides through Copper(I)-Catalyzed Finkelstein-Type Halide-Exchange Reaction

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2733
Armstrong, Ian S.; Bergmeier, Stephen C.: Development of a Method for the Synthesis of 4-Aryl-Functionalized 2-Azabicyclo[3.2.1]octanes

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2743
Kazmaier, Uli; Doroshenko, Tamara; Bauer, Kevin; Filbrich, Isabel; Grueter, Andreas; Jung, Gregor; Ullrich, Angelika: Coumaryl Triflate, a Versatile Building Block for the Modification of Coumarins and for Fluorescence Labeling

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2749
Wang, Kongchen; Bates, Roderick W.: Rhodium-Catalysed Hydroboration of Terminal Alkynes Using Pinacolborane Promoted by Tri(2-furyl)phosphine

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2753
Voskressensky, Leonid G.; Storozhenko, Olga A.; Festa, Alexey A.; Novikov, Roman A.; Varlamov, Alexey V.: Synthesis of Chromenoimidazoles, Annulated with an Azaindole Moiety, through a Base-Promoted Domino Reaction of Cyanomethyl Quaternary Salts Open Access

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2761
Park, Heemin; Kwon, Yongseok; Shin, Jae Eui; Kim, Woo-Jung; Hwang, Soonho; Lee, Seokwoo; Kim, Sanghee: Orthoester in Cyclodehydration of Carbamate-Protected Amino Alcohols under Acidic Conditions

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2768
Puvvala, Srinu; Jadhav, Vinod D.; Narkhede, Umesh C.; Anji Karun, M. V. V. S. R. N.; Venkata Ramana Reddy, Ch.: First Total Synthesis of a Cytotoxic Derivative of the Natural Product Aaptamine

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2775
Mathias, Fanny; Kabri, Youssef; Crozet, Maxime D.; Vanelle, Patrice: Efficient Access to Original 6-Substituted 5-Nitro-2,3-dihydroimidazo[2,1-b]oxazoles

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errata
2786
Kasai, Noritaka; Maeda, Ryoko; Furuno, Hiroshi; Hanamoto, Takeshi: A Practical Synthesis and Applications of (E)-Diphenyl-β-(trifluoromethyl)vinylsulfonium Triflate FREE ACCESS

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