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- Reactivity and the mechanisms of reactions of β-sultams with nucleophiles. J. Matthew Wood, Paul S. Hinchliffe, Andrew P. Laws, Michael I. Page
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 938
-
Synthesis and inhibitory properties of
(1R,2R,4R,6
R)-6-O
-(2-hydroxyethyl)cyclohexane-1,2,4,6-tetraol derivatives: mechanistic
probes for the inositol monophosphatase
reaction 1
. Jürgen Schulz, David Gani
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 657
- Studies on the decomposition pathways of diastereoisomeric mixtures of aryl nucleoside α-hydroxyphosphonates under hydrolytic conditions. Synthesis of α-hydroxyphosphonate monoesters. Agnieszka Szymańska-Michalak, Jacek Stawiński, Adam Kraszewski
, New J. Chem.
, 2010
, 34
, 976
- The reactivity of phosphate esters: reactions of monoesters with nucleophiles. Nucleophilicity independent of basicity in a bimolecular substitution reaction. A. J. Kirby, A. G. Varvoglis
, J. Chem. Soc. B
, 1968
, 135
- Recognition of phosphate monoester dianion by an alkoxide-bridged dinuclear zinc(ii) complex. Eiji Kinoshita, Makoto Takahashi, Hironori Takeda, Motoo Shiro, Tohru Koike
, Dalton Trans.
, 2004
, 1189
- Mechanism of the solvolysis of allylic diphenyl phosphates in phenol. J. A. Miller
, J. Chem. Soc. B
, 1968
, 1427
- The α-hydroxyphosphonate-phosphate rearrangement of a noncyclic substrate – some new observations. Susanne Prechelmacher, Kurt Mereiter, Friedrich Hammerschmidt
, Org. Biomol. Chem.
, 2018
, 16
, 3672
- Intramolecular general acid catalysis of phosphate monoester hydrolysis. The hydrolysis of salicyl phosphate. R. H. Bromilow, A. J. Kirby
, J. Chem. Soc., Perkin Trans. 2
, 1972
, 149
- Determination of absolute configuration of the phosphonic acid moiety of fosfazinomycins. Katharina Schiessl, Alexander Roller, Friedrich Hammerschmidt
, Org. Biomol. Chem.
, 2013
, 11
, 7420
- 223. Studies on phosphorylation. Part X. The preparation of tetraesters of pyrophosphoric acid from diesters of phosphoric acid by means of exchange reactions. N. S. Corby, G. W. Kenner, A. R. Todd
, J. Chem. Soc.
, 1952
, 1234