DOI: 10.1055/s-00000083

Synlett

Issue 10 · Volume 30 · June 2019 DOI: 10.1055/s-009-43199

table of contents

V
Linked PDF of Table of Contents

synpacts

1105
Hu, Yue; Sun, Wei; Liu, Chao: Deoxygenative Transformation of Carbonyl and Carboxyl Compounds Using gem-Diborylalkanes
https://www.thieme-connect.de/media/synlett/201910/i_p0012_ga_10-1055_s-0037-1611728.gif

account

1111
Hu, Ben-Lin; Baumgarten, Martin: Thiadiazoloquinoxalines
https://www.thieme-connect.de/media/synlett/201910/i_a0009_ga_10-1055_s-0037-1611739.gif
1125
Kamitanaka, Tohru; Morimoto, Koji; Dohi, Toshifumi; Kita, Yasuyuki: Controlled-Coupling of Quinone Monoacetals by New Activation Methods: Regioselective Synthesis of Phenol-Derived Compounds
https://www.thieme-connect.de/media/synlett/201910/i_a0832_ga_10-1055_s-0037-1611735.gif

cluster

1144
Cluster Cover Page
https://www.thieme-connect.de/media/synlett/201910/i_st-10_clustercover_10-1055_s-0039-1689983.jpg
1147
Kawamata, Yu; Baran, Phil S.: Cluster Preface: Electrochemical Synthesis and Catalysis
https://www.thieme-connect.de/media/synlett/201910/i_b2222_ga_10-1055_s-0039-1689970.jpg
1149
Song, Chunlan; Liu, Kun; Dong, Xin; Chiang, Chien-Wei; Lei, Aiwen: Recent Advances in Electrochemical Oxidative Cross-Coupling for the Construction of C–S Bonds
https://www.thieme-connect.de/media/synlett/201910/i_b0046_ga_10-1055_s-0037-1611753.gif
1164
Qiu, Youai; Struwe, Julia; Ackermann, Lutz: Metallaelectro-Catalyzed C–H Activation by Weak Coordination
https://www.thieme-connect.de/media/synlett/201910/i_a0128_ga_10-1055_s-0037-1611568.gif
1174
Lips, Sebastian; Franke, Robert; Waldvogel, Siegfried R.: Electrochemical Synthesis of 2-Hydroxy-para-terphenyls by Dehydrogenative Anodic C–C Cross-Coupling Reaction
https://www.thieme-connect.de/media/synlett/201910/i_b0749_ga_10-1055_s-0037-1611942.gif
Supporting Information
1178
Takahira, Yusuke; Chen, Miao; Kawamata, Yu; Mykhailiuk, Pavel; Nakamura, Hugh; Peters, Byron K.; Reisberg, Solomon H.; Li, Chao; Chen, Longrui; Hoshikawa, Tamaki; Shibuguchi, Tomoyuki; Baran, Phil S.: Electrochemical C(sp3)–H Fluorination
https://www.thieme-connect.de/media/synlett/201910/i_b1827_ga_10-1055_s-0037-1611737.gif
Supporting Information
1183
Amri, Nasser; Skilton, Ryan A.; Guthrie, Duncan; Wirth, Thomas: Efficient Flow Electrochemical Alkoxylation of Pyrrolidine-1-carbaldehyde
https://www.thieme-connect.de/media/synlett/201910/i_b0059_ga_10-1055_s-0037-1611774.gif
Supporting Information
1187
Klunder, Kevin J.; Cass, Ashley C.; Anderson, Scott L.; Minteer, Shelley D.: Phthalocyanines as a π–π Adsorption Strategy to Immobilize Catalyst on Carbon for Electrochemical Synthesis
https://www.thieme-connect.de/media/synlett/201910/i_b0068_ga_10-1055_s-0037-1611792.gif
Supporting Information
1194
Tanaka, Kenta; Yoshizawa, Hirona; Atobe, Mahito: A Flow Microreactor Approach to a Highly Efficient Diels–Alder Reaction with an Electrogenerated o-Quinone
https://www.thieme-connect.de/media/synlett/201910/i_b0804_ga_10-1055_s-0037-1611725.gif
Supporting Information
1199
Lu, Lingxiang; Fu, Niankai; Lin, Song: Three-Component Chlorophosphinoylation of Alkenes via Anodically Coupled Electrolysis
https://www.thieme-connect.de/media/synlett/201910/i_b0227_ga_10-1055_s-0039-1689934.gif
Supporting Information
1204
Yamamoto, Kosuke; Ishimaru, Keiko; Mizuta, Satoshi; Minato, Daishirou; Kuriyama, Masami; Onomura, Osamu: Diastereodivergent Synthesis of Bromoiminolactones: Electrochemical and Chemical Bromoiminolactonization of α-Allylmalonamides
https://www.thieme-connect.de/media/synlett/201910/i_b0057_ga_10-1055_s-0037-1611791.gif
Supporting Information
1209
Mitsudo, Koichi; Yoshioka, Kazuki; Hirata, Takayuki; Mandai, Hiroki; Midorikawa, Koji; Suga, Seiji: 1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides
https://www.thieme-connect.de/media/synlett/201910/i_b0070_ga_10-1055_s-0037-1611793.gif
Supporting Information
1215
Pandolfi, Fabiana; Chiarotto, Isabella; Mattiello, Leonardo; Rocco, Daniele; Feroci, Marta: Cathodic Reduction of Caffeine: Synthesis of an Amino-Functionalized Imidazole from a Biobased Reagent
https://www.thieme-connect.de/media/synlett/201910/i_b0076_ga_10-1055_s-0037-1611483.gif
Supporting Information
1219
Xu, P.; Xu, H.-C.: Electrochemical Deoxygenation of N-Heteroaromatic N-Oxides
https://www.thieme-connect.de/media/synlett/201910/i_b0117_ga_10-1055_s-0037-1611541.gif
Supporting Information

letter

1222
Jain, Nikita; Hein, Jason E.; Ciufolini, Marco A.: Oxidative Cyclization of Naphtholic Sulfonamides Mediated by a Chiral Hypervalent Iodine Reagent: Asymmetric Synthesis versus Resolution
https://www.thieme-connect.de/media/synlett/201910/i_r0107_ga_10-1055_s-0037-1611831.gif
Supporting Information
1228
Fei, Zhongbo; Xiong, Xin; Cheung, Chiming; Liu, Weipeng; Shen, Qirong; Zhang, Jinzhu; Gao, Hongjun; Bian, Jianwei: Asymmetric Synthesis of cis-(S,R)-3-Amino-4-fluoro-1-methylpyrrolidine
https://www.thieme-connect.de/media/synlett/201910/i_v0148_ga_10-1055_s-0037-1611553.gif
Supporting Information
1231
Karadeniz, Eda; Zora, Metin: One-Pot Synthesis of Spiro-2H-pyrroles from N-Propargylic β-Enaminones
https://www.thieme-connect.de/media/synlett/201910/i_d0116_ga_10-1055_s-0037-1611816.gif
Supporting Information
1237
Almahli, Hadia; Jimenez, Niamh C.; Moloney, Mark G.: Intramolecular Aldol Ring Closures of Cysteine Derivatives Leading to Densely Functionalised Pyroglutamates
https://www.thieme-connect.de/media/synlett/201910/i_d0141_ga_10-1055_s-0037-1611829.gif
Supporting Information
1241
Wu, Haiyan; Liu, Hongxin; Li, Juan; Li, Xinhua; Xiao, Hong-Ping; Jiang, Jun: Amino Acid Salt Catalyzed Asymmetric Addition Reaction of Acetylacetone to Maleimides and 2-(2-Oxoindolin-3-ylidene)malononitriles
https://www.thieme-connect.de/media/synlett/201910/i_l0129_ga_10-1055_s-0037-1610713.gif
Supporting Information
1246
Philips, Aimee; Cunningham, Christopher; Naran, Kajal; Kesharwani, Tanay: Synthesis of 3-Halo-7-azaindoles through a 5-endo-dig Electrophilic Cyclization Reaction
https://www.thieme-connect.de/media/synlett/201910/i_v0112_ga_10-1055_s-0037-1611827.gif
Supporting Information