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- 144. Reactions of carbinols in the presence of alkali. Part III. The scission of αβ-ethylenic carbinols. G. H. Hargreaves, L. N. Owen
, J. Chem. Soc.
, 1947
, 756
-
Synthesis of chiral tricyclo[3.2.1.02,7]octanes by an
efficient 3-exo-trig radical cyclisation
reaction 1
. Adusumilli Srikrishna, G. Veera Raghava Sharma
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 177
- Prins reaction under manganese dioxide control: the synthesis of 6-oxa-2-azabicyclo[3.2.1]octan-4-ones from tetrahydropyridines and formaldehyde. Anatoly T. Soldatenkov, Kyrill B. Polyanskii, Ayalew W. Temesgen, Svetlana A. Soldatova, Nataliya D. Sergeeva, Nadezhda M. Kolyadina, Nikolai N. Lobanov
, Mendeleev Commun.
, 2001
, 11
, 27
- Substrate-oriented selectivity in the Mg-mediated conjugate addition of bromoform to electron-deficient alkenes. Nishikant Satam, Saumyadip Nemu, Guddeangadi N. Gururaja, Irishi N. N. Namboothiri
, Org. Biomol. Chem.
, 2020
, 18
, 5697
- Enzymatic reduction of levoglucosenone by an alkene reductase (OYE 2.6): a sustainable metal- and dihydrogen-free access to the bio-based solvent Cyrene®. Louis M. M. Mouterde, Florent Allais, Jon D. Stewart
, Green Chem.
, 2018
, 20
, 5528
- Isomerisation of epoxides to carbonyl compounds induced by iodides in dimethyl sulphoxide. D. Bethell, G. W. Kenner, P. J. Powers
, Chem. Commun. (London)
, 1968
, 227
- Homoconjugate addition to spiro[2.5]octen-4-ones. P. Hugh Helferty, Paul Mahler, Peter Yates
, J. Chem. Soc., Chem. Commun.
, 1979
, 1084
- Participation of sulphonamide nitrogen in the rearrangement of the 2-azabicyclo[2.2.2]octane skeleton: an efficient synthesis of the 6-azabicyclo[3.2.1]octan-4-one system. Andrew B. Holmes, Paul R. Raithby, John Thompson, Andrew J. G. Baxter, John Dixon
, J. Chem. Soc., Chem. Commun.
, 1983
, 1490
- 142. Reactions of carbinols in the presence of alkali. Part I. The reduction of ketones by primary alcohols. G. H. Hargreaves, L. N. Owen
, J. Chem. Soc.
, 1947
, 750
- Triplet-sensitised di-π-methane rearrangement of N-substituted 2-azabarrelenones. Andreas Tröster, Thorsten Bach
, Chem. Commun.
, 2019
, 55
, 302