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- XXI.—The chlorination of iodophenols. Part III. The chlorination of o-iodophenol. Samuel Buchan, Hamilton McCombie
, J. Chem. Soc.
, 1931
, 137
- An efficient cascade synthesis of various 2H-1,4-benzoxazin-3-(4H)-ones from o-halophenols and 2-halo-amides catalyzed by CuI. Dingben Chen, Guodong Shen, Weiliang Bao
, Org. Biomol. Chem.
, 2009
, 7
, 4067
- Palladium-catalysed heteroannulation with acetylenic compounds: synthesis of benzofurans1. Nitya G. Kundu, Manojit Pal, Jyan S. Mahanty, Mahuya De
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2815
- Total synthesis of natural products containing benzofuran rings. Majid M. Heravi, Vahideh Zadsirjan, Hoda Hamidi, Parvin Hajiabbas Tabar Amiri
, RSC Adv.
, 2017
, 7
, 24470
- Indium-catalyzed polycyclotrimerization of diynes: a facile route to prepare regioregular hyperbranched polyarylenes. Zhe Wang, Yang Shi, Jian Wang, Lingzhi Li, Haiqiang Wu, Bicheng Yao, Jing Zhi Sun, Anjun Qin, Ben Zhong Tang
, Polym. Chem.
, 2014
, 5
, 5890
- Determination of iodinated phenol species at parts-per-trillion concentration levels in different water samples by solid-phase microextraction/offline GC-ICP-MS. Rodolfo G. Wuilloud, Jorgelina C. A. de Wuilloud, Anne P. Vonderheide, Joseph A. Caruso
, J. Anal. At. Spectrom.
, 2003
, 18
, 1119
- [PhSiO1.5]8,10,12 as nanoreactors for non-enzymatic introduction of ortho, meta or para-hydroxyl groups to aromatic molecules. Mozhgan Bahrami, Xingwen Zhang, Morteza Ehsani, Yousef Jahani, Richard M. Laine
, Dalton Trans.
, 2017
, 46
, 8797
- Are the three hydroxyphenyl radical isomers created equal? – The role of the phenoxy radical –. P. Hemberger, G. da Silva, A. J. Trevitt, T. Gerber, A. Bodi
, Phys. Chem. Chem. Phys.
, 2015
, 17
, 30076
- A study of the crystal and molecular structures of phenols with only intermolecular hydrogen bonding. Keith Prout, John Fail, Richard M. Jones, Rachael E. Warner, John C. Emmett
, J. Chem. Soc., Perkin Trans. 2
, 1988
, 265
- Nature of hydrogen-bond-enhanced halogen bonding viewed through electron density changes. Hajime Torii, Akari Kimura, Takanori Sakai
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 17951