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- Structural variations in rare earth benzoate complexes Part I. Lanthanum. Hendrik Bußkamp, Glen B. Deacon, Matthias Hilder, Peter C. Junk, Ulrich H. Kynast, Winnie W. Lee, David R. Turner
, CrystEngComm
, 2007
, 9
, 394
- 254. Curare alkaloids. Part IV. Bebeerine and tubocurarine. Orientation of phenolic groups. Harold King
, J. Chem. Soc.
, 1939
, 1157
- Dual mode of action of phenyl-pyrazole-phenyl (6-5-6 system)-based PPI inhibitors: alpha-helix backbone versus alpha-helix binding epitope. Natalya I. Vasilevich, Ilya I. Afanasyev, Eugene A. Rastorguev, Dmitry V. Genis, Valery S. Kochubey
, Med. Chem. Commun.
, 2013
, 4
, 1597
- Design, synthesis and evaluation of l-quebrachitol derivatives against α-glycosidase. Maoying Zhang, Xinjie Liang, Pengcheng Cai, Qixun Feng, Yongsong Chen, Xiaoxi Yu, Kuo Zhang, Xuefei Bao, Guoliang Chen
, New J. Chem.
, 2023
, 47
, 13387
- Upgrading malic acid to bio-based benzoates via a Diels–Alder-initiated sequence with the methyl coumalate platform. Jennifer J. Lee, Gerald R. Pollock III, Donald Mitchell, Lindsay Kasuga, George A. Kraus
, RSC Adv.
, 2014
, 4
, 45657
- The dependency of twist-bend nematic liquid crystals on molecular structure: a progression from dimers to trimers, oligomers and polymers. Richard J. Mandle
, Soft Matter
, 2016
, 12
, 7883
- Organocatalytic asymmetric Michael/hemiacetalization/acyl transfer reaction of α-nitroketones with o-hydroxycinnamaldehydes: synthesis of 2,4-disubstituted chromans. Rajendra Maity, Subhas Chandra Pan
, Org. Biomol. Chem.
, 2018
, 16
, 1598
- Formula index
, J. Chem. Soc.
, 1939
, 1998
- Tailoring pores for guest entrapment in a unimolecular surface self-assembled hydrogen bonded network. Anna G. Phillips, Luís M. A. Perdigão, Peter H. Beton, Neil R. Champness
, Chem. Commun.
, 2010
, 46
, 2775
- Ligand-free Cu(ii)-catalyzed aerobic etherification of aryl halides with silanes: an experimental and theoretical approach. Muhammad Naeem Ahmed, Khalil Ahmad, Khawaja Ansar Yasin, Tayyaba Farooq, Bilal Ahmad Khan, Soumendra K. Roy
, New J. Chem.
, 2019
, 43
, 11316