Synthesis of medium-sized (6–7–6) ring compounds by iron-catalyzed dehydrogenative C–H activation/annulation

Niranjan Panda, Irshad Mattan, Subhadra Ojha and Chandra Shekhar Purohit

Org. Biomol. Chem., 2018, 16, 7861
DOI: 10.1039/C8OB01496E

Synthesis, structure, self-assembly and genotoxicity evaluation of a series of Mn-Anderson cluster based polyoxometalate–organic hybrids

V. S. V. Satyanarayana, Pulikanti Guruprasad Reddy and Chullikkattil P. Pradeep

RSC Adv., 2015, 5, 59609
DOI: 10.1039/C5RA07581E

Synthesis of a novel polycyclic ring scaffold with antimitotic properties via a selective domino Heck–Suzuki reaction

Esther Alza, Luca Laraia, Brett M. Ibbeson, Súil Collins, Warren R. J. D. Galloway, Jamie E. Stokes, Ashok R. Venkitaraman and David R. Spring

Chem. Sci., 2015, 6, 390
DOI: 10.1039/C4SC02547D

Natural product analogues: towards a blueprint for analogue-focused synthesis

Magnus W. P. Bebbington

Chem. Soc. Rev., 2017, 46, 5059
DOI: 10.1039/C6CS00842A

Synthesis of Ellagitannins Containing Axial-Rich Glucose

Hidetoshi Yamada, Yasunori Ikeda, Kohei Nagao and Yusuke Kasai

J. Synth. Org. Chem. Jpn., 2013, 71, 1051
DOI: 10.5059/yukigoseikyokaishi.71.1051

Copper(II)‐Amine Complex‐Mediated Intramolecular Coupling of Gallates: A Bioinspired Solution to the Atroposelective Synthesis of Ellagitannins

Romain Larrieu, Antoine Richieu, Anaëlle Cornu, Nicolas Daugey, Laurent Pouységu, Denis Deffieux and Stéphane Quideau

Angewandte Chemie, 2024, 136
DOI: 10.1002/ange.202412036

High-Yield Total Synthesis of (−)-Strictinin through Intramolecular Coupling of Gallates

Naoki Michihata, Yuki Kaneko, Yusuke Kasai, Kotaro Tanigawa, Tsukasa Hirokane, Sho Higasa and Hidetoshi Yamada

J. Org. Chem., 2013, 78, 4319
DOI: 10.1021/jo4003135

Pedunculagin and tellimagrandin-I stimulate inflammation and angiogenesis and upregulate vascular endothelial growth factor and tumor necrosis factor-alpha in vivo

Amanda Silva Fernandes, Abel Vieira de Melo Bisneto, Luana Santos Silva, Elisa Flávia Luiz Cardoso Bailão, Clever Gomes Cardoso, Cristiene Costa Carneiro, Suzana da Costa Santos and Lee Chen-Chen

Microvascular Research, 2024, 151, 104615
DOI: 10.1016/j.mvr.2023.104615

Efficient Suzuki–Miyaura C-C Cross-Couplings Induced by Novel Heterodinuclear Pd-bpydc-Ln Scaffolds

Fu Ding, Yanli Li, Pingxuan Yan, Yan Deng, Dongping Wang, Yajing Zhang, Ileana Dragutan, Valerian Dragutan and Kangjun Wang

Molecules, 2018, 23, 2435
DOI: 10.3390/molecules23102435

Synthesis and biological evaluations of a series of calycanthaceous analogues as antifungal agents

Shaojun Zheng, Rui Zhu, Bing Tang, Lizhuang Chen, Hongjin Bai and Jiwen Zhang

Natural Product Research, 2021, 35, 1816
DOI: 10.1080/14786419.2019.1644635

Copper(II)‐Amine Complex‐Mediated Intramolecular Coupling of Gallates: A Bioinspired Solution to the Atroposelective Synthesis of Ellagitannins

Romain Larrieu, Antoine Richieu, Anaëlle Cornu, Nicolas Daugey, Laurent Pouységu, Denis Deffieux and Stéphane Quideau

Angew Chem Int Ed, 2024, 63
DOI: 10.1002/anie.202412036

Palladium‐Catalysed Cross‐Coupling of Vinyldisiloxanes with Benzylic and Allylic Halides and Sulfonates

Elizabeth C. Frye, Cornelius J. O' Connor, David G. Twigg, Bryony Elbert, Luca Laraia, David G. Hulcoop, Ashok R. Venkitaraman and David R. Spring

Chemistry A European J, 2012, 18, 8774
DOI: 10.1002/chem.201200431

Total Synthesis of (+)‐Davidiin

Yusuke Kasai, Naoki Michihata, Hidehisa Nishimura, Tsukasa Hirokane and Hidetoshi Yamada

Angew Chem Int Ed, 2012, 51, 8026
DOI: 10.1002/anie.201203305

Diversity-oriented synthesis as a tool for identifying new modulators of mitosis

Brett M. Ibbeson, Luca Laraia, Esther Alza, Cornelius J. O' Connor, Yaw Sing Tan, Huw M.L. Davies, Grahame McKenzie, Ashok R. Venkitaraman and David R. Spring

Nat Commun, 2014, 5
DOI: 10.1038/ncomms4155

Development of Methodologies toward the Unified Synthesis of Ellagitannins

Kazutada Ikeuchi

Chem. Pharm. Bull., 2024, 72, 349
DOI: 10.1248/cpb.c23-00920

CuI-Zeolite Catalysis for Biaryl Synthesis via Homocoupling Reactions of Phenols or Aryl Boronic Acids

Xiaohui Di, Tony Garnier, Arnaud Clerc, Eliott Jung, Christian Lherbet, Valérie Bénéteau, Patrick Pale and Stefan Chassaing

Molecules, 2024, 29, 5552
DOI: 10.3390/molecules29235552

A Pharmacological Review of Bioactive Constituents ofPaeonia lactifloraPallas andPaeonia veitchiiLynch

Shefton Parker, Brian May, Claire Zhang, Anthony Lin Zhang, Chuanjian Lu and Charlie Changli Xue

Phytother. Res., 2016, 30, 1445
DOI: 10.1002/ptr.5653

Synthesis of Benzannulated Medium‐ring Lactams via a Tandem Oxidative Dearomatization‐Ring Expansion Reaction

Tezcan Guney, Todd A. Wenderski, Matthew W. Boudreau and Derek S. Tan

Chemistry A European J, 2018, 24, 13150
DOI: 10.1002/chem.201802880

Synthesis and biological evaluation of calycanthaceous alkaloid analogs

Shaojun Zheng, Rui Zhu, Xinping Zhou, Lizhuang Chen, Hongjin Bai and Jiwen Zhang

Bioorganic & Medicinal Chemistry, 2019, 27, 115088
DOI: 10.1016/j.bmc.2019.115088

Synthesis and Comparative Structure–Activity Study of Carbohydrate-Based Phenolic Compounds as α-Glucosidase Inhibitors and Antioxidants

Shota Machida, Saki Mukai, Rina Kono, Megumi Funato, Hiroaki Saito and Taketo Uchiyama

Molecules, 2019, 24, 4340
DOI: 10.3390/molecules24234340

Fast Pyrolysis of 13C-Labeled Cellobioses: Gaining Insights into the Mechanisms of Fast Pyrolysis of Carbohydrates

John C. Degenstein, Priya Murria, Mckay Easton, Huaming Sheng, Matt Hurt, Alex R. Dow, Jinshan Gao, John J. Nash, Rakesh Agrawal, W. Nicholas Delgass, Fabio H. Ribeiro and Hilkka I. Kenttämaa

J. Org. Chem., 2015, 80, 1909
DOI: 10.1021/jo5025255

Fundamental Methods in Ellagitannin Synthesis

Hidetoshi Yamada, Tsukasa Hirokane, Kazutada Ikeuchi and Shinnosuke Wakamori

Natural Product Communications, 2017, 12
DOI: 10.1177/1934578X1701200846

Synthesis and Antimicrobial Activity of Calycanthaceous Derivatives

Rui Zhu, Cheng Yang, Ke Han, Yongdong Gu, Jiwen Zhang, Shaojun Zheng and Hongjin Bai

Natural Product Communications, 2021, 16
DOI: 10.1177/1934578X211032611

Total Synthesis of (+)‐Davidiin

Yusuke Kasai, Naoki Michihata, Hidehisa Nishimura, Tsukasa Hirokane and Hidetoshi Yamada

Angewandte Chemie, 2012, 124, 8150
DOI: 10.1002/ange.201203305

Synthesis of a Ribose‐Incorporating Medium Ring Scaffold via a Challenging Ring‐Closing Metathesis Reaction

Stuart S. Rankin, John J. Caldwell, Nora B. Cronin, Rob L. M. van Montfort and Ian Collins

Eur J Org Chem, 2016, 2016, 4496
DOI: 10.1002/ejoc.201600756

Small-Molecule Inhibitors of Reactive Oxygen Species Production

Elisa Sassetti, Mads H. Clausen and Luca Laraia

J. Med. Chem., 2021, 64, 5252
DOI: 10.1021/acs.jmedchem.0c01914

Non‐Enzymatic Oxidation of a Pentagalloylglucose Analogue into Members of the Ellagitannin Family

Seiya Ashibe, Kazutada Ikeuchi, Yuji Kume, Shinnosuke Wakamori, Yuri Ueno, Takashi Iwashita and Hidetoshi Yamada

Angew Chem Int Ed, 2017, 56, 15402
DOI: 10.1002/anie.201708703

Non‐Enzymatic Oxidation of a Pentagalloylglucose Analogue into Members of the Ellagitannin Family

Seiya Ashibe, Kazutada Ikeuchi, Yuji Kume, Shinnosuke Wakamori, Yuri Ueno, Takashi Iwashita and Hidetoshi Yamada

Angewandte Chemie, 2017, 129, 15604
DOI: 10.1002/ange.201708703

Synthesis of Lactonized Valoneoyl Group-Containing Ellagitannins, Oenothein C and Cornusiin B

Hitoshi Abe, Haruka Imai, Daichi Ogura and Yoshikazu Horino

HETEROCYCLES, 2020, 101, 524
DOI: 10.3987/COM-19-S(F)42

Total Synthesis of Phyllanemblinin B

Shintaro Matsumoto, Shinnosuke Wakamori, Kentaro Nishii, Takashi Tanaka and Hidetoshi Yamada

Synlett, 2020, 31, 1389
DOI: 10.1055/s-0040-1707812

Advancement of Organic Chemical Synthetic Methods in Ellagitannins

Shinnosuke WAKAMORI and Reina KUSUKI

KAGAKU TO SEIBUTSU, 2022, 60, 502
DOI: 10.1271/kagakutoseibutsu.60.502

Direct Glycosylation of Bioactive Small Molecules with Glycosyl Iodide and Strained Olefin as Acid Scavenger

Xiangying Gu, Lin Chen, Xin Wang, Xiao Liu, Qidong You, Wenwei Xi, Li Gao, Guohua Chen, Yue-Lei Chen, Bing Xiong and Jingkang Shen

J. Org. Chem., 2014, 79, 1100
DOI: 10.1021/jo402551x

In silico studies evidenced the role of structurally diverse plant secondary metabolites in reducing SARS-CoV-2 pathogenesis

Hariprasad Puttaswamy, Hittanahallikoppal Gajendramurthy Gowtham, Monu Dinesh Ojha, Ajay Yadav, Gourav Choudhir, Vasantharaja Raguraman, Bhani Kongkham, Koushalya Selvaraju, Shazia Shareef, Priyanka Gehlot, Faiz Ahamed and Leena Chauhan

Sci Rep, 2020, 10
DOI: 10.1038/s41598-020-77602-0

Total Syntheses of Laevigatins A and E

Tsukasa Hirokane, Kazutada Ikeuchi and Hidetoshi Yamada

Eur J Org Chem, 2015, 2015, 7352
DOI: 10.1002/ejoc.201501037

First Total Synthesis of Neostrictinin

Kazutada Ikeuchi, Tatsuya Ueji, Shintaro Matsumoto, Shinnosuke Wakamori and Hidetoshi Yamada

Eur J Org Chem, 2020, 2020, 2077
DOI: 10.1002/ejoc.202000053

Interglycosidic C5–C6 rotamer distributions of alkyl O-rutinosides

Dhwani Mehta and Carlos A. Sanhueza

Carbohydrate Research, 2024, 544, 109251
DOI: 10.1016/j.carres.2024.109251

Ellagitannins from Eucalyptus camaldulensis and their potential use in the food industry

Eliseo Sánchez-Loredo, Leonardo Sepúlveda, Jorge E. Wong-Paz, Lissethe Palomo-Ligas, Raúl Rodriguez-Herrera, Cristóbal N. Aguilar and Juan A. Ascacio-Valdés

Explor Foods Foodomics, 2024, 2, 83
DOI: 10.37349/eff.2024.00027

Oenothein B, dimeric hydrolysable tannin inhibiting HCV invasion from Oenothera erythrosepala

Satoru Tamura, Gang-Ming Yang, Teruaki Koitabashi, Yoshiharu Matsuura, Yasumasa Komoda, Tomikazu Kawano and Nobutoshi Murakami

J Nat Med, 2019, 73, 67
DOI: 10.1007/s11418-018-1239-1

Phenolic compounds as antiviral agents: An In-Silico investigation against essential proteins of SARS-CoV-2

Hammami Majdi, Feten Zar Kalai, Walid Yeddess and Moufida Saidani

NRFHH, 2021, 2, 62
DOI: 10.53365/nrfhh/143085

Development of Methods Aimed at Syntheses of All Ellagitannins

Kazutada Ikeuchi, Shinnosuke Wakamori, Tsukasa Hirokane and Hidetoshi Yamada

J. Syn. Org. Chem., Jpn., 2018, 76, 904
DOI: 10.5059/yukigoseikyokaishi.76.904

A Palladium‐Catalyzed Carbonylation Approach to Eight‐Membered Lactam Derivatives with Antitumor Activity

Raffaella Mancuso, Dnyaneshwar S. Raut, Nadia Marino, Giorgio De Luca, Cinzia Giordano, Stefania Catalano, Ines Barone, Sebastiano Andò and Bartolo Gabriele

Chemistry A European J, 2016, 22, 3053
DOI: 10.1002/chem.201504443

Structural Simplification of Natural Products

Shengzheng Wang, Guoqiang Dong and Chunquan Sheng

Chem. Rev., 2019, 119, 4180
DOI: 10.1021/acs.chemrev.8b00504