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- A stable adduct of sodium ethanethiolate attack at the C-7 ring carbon of 2-ethylthiotropone: stabilisation of a base adduct to an unsubstituted cycloheptatrienone ring carbon by bivalent sulphur. Carlo A. Veracini, Francesco Pietra
, J. Chem. Soc., Chem. Commun.
, 1974
, 623
- 2′,3′-Anhydrouridine. A useful synthetic intermediate. Anwar Miah, Colin B. Reese, Quanlai Song, Zoë Sturdy, Stephen Neidle, Ian J. Simpson, Martin Read, Emma Rayner
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 3277
- The reaction of elemental phosphorus with alkanethiolates in the presence of tetrachloromethane. Charles Brown, Robert F. Hudson, Gary A. Wartew
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 1799
- σ-Complex formation and aromatic substitution with thiolates and nitroaryl thioethers. Gino Biggi, Francesco Pietra
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 1980
- Solvent effects on the relative stabilities of 1:1 and 1:2 adducts formed from 1,3,5-trinitrobenzene and thiolate ions. M. R. Crampton, M. El. Ghariani
, J. Chem. Soc. B
, 1971
, 1043
- Eliminations promoted by thiolate ions. Part I. Kinetics and mechanism of the reaction of DDT with sodium benzenethiolate and other nucleophiles. B. D. England, D. J. McLennan
, J. Chem. Soc. B
, 1966
, 696
- Preparation of optically active azophenolic crown ethers containing 1-phenylethane-1,2-diol and 2,4-dimethyl-3-oxapentane-1,5-diol as a chiral subunit: temperature-dependent enantiomer selectivity in the complexation with chiral amines 1. Kazuko Ogasahara, Keiji Hirose, Yoshito Tobe, Koichiro Naemura
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 3227
- Chemical consequences of the intramolecular interaction between a sulphur atom and a methoxycarbonyl group in fluorene systems. Warō Nakanishi, Yoshiaki Kusuyama, Yoshitsugu Ikeda, Michinori Ōki
, J. Chem. Soc., Perkin Trans. 2
, 1986
, 799
- One-pot synthesis and characterization of chalcopyrite CuInS2 nanoparticles. Chivin Sun, Zehra Cevher, Jin Zhang, Bo Gao, Kai Shum, Yuhang Ren
, J. Mater. Chem. A
, 2014
, 2
, 10629
- Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack. Ismail Awheda, Nezire Saygili, A. Christopher Garner, John D. Wallis
, RSC Adv.
, 2013
, 3
, 24997