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- Synthetic transformation of hydroxymatairesinol from Norway spruce (Picea abies) to 7-hydroxysecoisolariciresinol, (+)-lariciresinol and (+)-cyclolariciresinol. Patrik Eklund, Reijo Sillanpää, Rainer Sjöholm
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 1906
- Reactions of the natural lignan hydroxymatairesinol in basic and acidic nucleophilic media: formation and reactivity of a quinone methide intermediate. Patrik C. Eklund, Fredrik J. Sundell, Annika I. Smeds, Rainer E. Sjöholm
, Org. Biomol. Chem.
, 2004
, 2
, 2229
- In silico study of natural compounds from sesame against COVID-19 by targeting Mpro, PLpro and RdRp. Ahmed E. Allam, Yhiya Amen, Ahmed Ashour, Hamdy K. Assaf, Heba Ali Hassan, Islam M. Abdel-Rahman, Ahmed M. Sayed, Kuniyoshi Shimizu
, RSC Adv.
, 2021
, 11
, 22398
- Chemical studies on antioxidant mechanisms and free radical scavenging properties of lignans. Patrik C. Eklund, Otto K. Långvik, Johan P. Wärnå, Tapio O. Salmi, Stefan M. Willför, Rainer E. Sjöholm
, Org. Biomol. Chem.
, 2005
, 3
, 3336
- Enhanced extraction and biological activity of 7-hydroxymatairesinol obtained from Norway spruce knots using aqueous solutions of ionic liquids. Ana M. Ferreira, Eduarda S. Morais, Ana Cláudia Leite, Aminou Mohamadou, Bjarne Holmbom, Thomas Holmbom, Bruno M. Neves, João A. P. Coutinho, Mara G. Freire, Armando J. D. Silvestre
, Green Chem.
, 2017
, 19
, 2626
- Asymmetric synthesis, stereochemistry and rearrangement reactions of naturally occurring 7′-hydroxylignano-9,9′-lactones. Barbara Raffaelli, Kristiina Wähälä, Tapio Hase
, Org. Biomol. Chem.
, 2006
, 4
, 331
- Recent strategies and tactics for the enantioselective total syntheses of cyclolignan natural products. Rebekah G. Reynolds, Huong Quynh Anh Nguyen, Jordan C. T. Reddel, Regan J. Thomson
, Nat. Prod. Rep.
, 2022
, 39
, 670
- An update on lignans: natural products and synthesis. Jian-Yu Pan, Shi-Lin Chen, Mei-Hua Yang, Jun Wu, Jari Sinkkonen, Kun Zou
, Nat. Prod. Rep.
, 2009
, 26
, 1251
- A selective de-O-methylation of guaiacyl lignans to corresponding catechol derivatives by 2-iodoxybenzoic acid (IBX). The role of the catechol moiety on the toxicity of lignans. Roberta Bernini, Maurizio Barontini, Pasquale Mosesso, Gaetano Pepe, Stefan M. Willför, Rainer E. Sjöholm, Patrik C. Eklund, Raffaele Saladino
, Org. Biomol. Chem.
, 2009
, 7
, 2367
- Stereochemistry and rearrangement reactions of hydroxylignanolactones. Barbara Raffaelli, Monika Pohjoispää, Tapio Hase, Christine J. Cardin, Yu Gan, Kristiina Wähälä
, Org. Biomol. Chem.
, 2008
, 6
, 2619