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- BF3·OEt2-mediated nucleophilic fluorocyclization of sulfonyl 3-methylene-oxabenzocyclooctan-6-ones. Diastereocontrolled synthesis of benzofused fluorooxabicyclo[4.2.1]nonanes. Nai-Chen Hsueh, Meng-Yang Chang
, Org. Biomol. Chem.
, 2022
, 20
, 7503
- Synthesis of novel trithiocarbonate and allyl sulfide containing monomers. Christopher R. Fenoli, Christopher N. Bowman
, Polym. Chem.
, 2014
, 5
, 62
- An alternative to ‘propylene/Leonard linker’ for studying arene interactions in flexible pyrazolo[3,4-d]pyrimidine core based models both at molecular and supramolecular levels. Kamlakar Avasthi, Amantullah Ansari, Ruchir Kant, Prakas R. Maulik, Krishnan Ravikumar, Partha Chattopadhyay, Nirmal D. Adhikary
, CrystEngComm
, 2011
, 13
, 2039
- Dual cellular stimuli-responsive hydrogel nanocapsules for delivery of anticancer drugs. Qiangying Yi, Jin Ma, Ke Kang, Zhongwei Gu
, J. Mater. Chem. B
, 2016
, 4
, 4922
- Amplification of chirality in N,N′-1,2-ethanediylbisbenzamides: from planar sheets to twisted ribbons. Fátima Aparicio, Felipe Vicente, Luis Sánchez
, Chem. Commun.
, 2010
, 46
, 8356
- Efficient syntheses of pterulone, pterulone B and related analogues. Philippe Lemaire, Geneviève Balme, Philippe Desbordes, Jean-Pierre Vors
, Org. Biomol. Chem.
, 2003
, 1
, 4209
- Design, synthesis and cytotoxic activity of water-soluble quinones with dibromo-p-benzoquinone cores and amino oligo(ethylene glycol) side chains against MCF-7 breast cancer cells. Leon F. Scherz, Engy A. Abdel-Rahman, Sameh S. Ali, A. Dieter Schlüter, Mona A. Abdel-Rahman
, Med. Chem. Commun.
, 2017
, 8
, 662
- Organizing multivalency in carbohydrate recognition. Christian Müller, Guillaume Despras, Thisbe K. Lindhorst
, Chem. Soc. Rev.
, 2016
, 45
, 3275
- Catalytic strategies towards 1,3-polyol synthesis by enantioselective cascades creating multiple alcohol functions. Céline Sperandio, Jean Rodriguez, Adrien Quintard
, Org. Biomol. Chem.
, 2020
, 18
, 1025
- Calix[4]arene daisychains. Soheila Sameni, Catherine Jeunesse, Dominique Matt, Jack Harrowfield
, Chem. Soc. Rev.
, 2009
, 38
, 2117