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Sokolov, V.I., Troitskaya, L.L., Khrushchova, N.S. (1983) Asymmetric cyclopalladation in the ferrocene series as a tool for enantioselective synthesis. Preparation of some analogues of natural products. Journal of Organometallic Chemistry, 250 (1) 439-446 doi:10.1016/0022-328x(83)85068-2

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Reference TypeJournal (article/letter/editorial)
TitleAsymmetric cyclopalladation in the ferrocene series as a tool for enantioselective synthesis. Preparation of some analogues of natural products
JournalJournal of Organometallic Chemistry
AuthorsSokolov, V.I.Author
Troitskaya, L.L.Author
Khrushchova, N.S.Author
Year1983 (July)Volume250
Issue1
PublisherElsevier BV
DOIdoi:10.1016/0022-328x(83)85068-2Search in ResearchGate
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Mindat Ref. ID14462238Long-form Identifiermindat:1:5:14462238:4
GUID0
Full ReferenceSokolov, V.I., Troitskaya, L.L., Khrushchova, N.S. (1983) Asymmetric cyclopalladation in the ferrocene series as a tool for enantioselective synthesis. Preparation of some analogues of natural products. Journal of Organometallic Chemistry, 250 (1) 439-446 doi:10.1016/0022-328x(83)85068-2
Plain TextSokolov, V.I., Troitskaya, L.L., Khrushchova, N.S. (1983) Asymmetric cyclopalladation in the ferrocene series as a tool for enantioselective synthesis. Preparation of some analogues of natural products. Journal of Organometallic Chemistry, 250 (1) 439-446 doi:10.1016/0022-328x(83)85068-2
In(1983, July) Journal of Organometallic Chemistry Vol. 250 (1) Elsevier BV

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SOKOLOV, V. I., TROITSKAYA, L. L., KHRUSHCHOVA, N. S. (1983) ChemInform Abstract: ASYMMETRIC CYCLOPALLADATION IN THE FERROCENE SERIES AS A TOOL FOR ENANTIOSELECTIVE SYNTHESIS. PREPARATION OF SOME ANALOGS OF NATURAL PRODUCTS. Chemischer Informationsdienst, 14 (44) doi:10.1002/chin.198344324
Sokolov, V.I., Troitskaya, L.L., Reutov, O.A. (1979) Asymmetric cyclopalladation of dimethylaminomethylferrocene. Journal of Organometallic Chemistry, 182 (4) 537-546 doi:10.1016/s0022-328x(00)83942-x
Sokolov, V.I., Troitskaya, L.L., Gautheron, B., Tainturier, G. (1982) Asymmetric cyclopalladation of 1′-dimethylamino-[3] ferrocenophane: central and planar chirality and the effect of conformational rigidity. Journal of Organometallic Chemistry, 235 (3) 369-373 doi:10.1016/s0022-328x(00)96090-x
Sokolov, V.I., Troitskaya, L.L., Reutov, O.A. (1977) Asymmetric induction in the course of internal palladation of enantiomeric 1-dimethylaminoethylferrocene. Journal of Organometallic Chemistry, 133 (2) doi:10.1016/s0022-328x(00)92883-3
Sokolov, V.I., Troitskaya, L.L., Khrushcheva, N.S., Reutov, O.A. (1989) Stereo- and enantioselectivity in catalytic hydrogenolysis of chiral substituted ferrocenes to give cyclopentanes. Journal of Organometallic Chemistry, 378 (2) 227-233 doi:10.1016/0022-328x(89)80010-5
Sokolov, V.I., Troitskaya, L.L., Reutov, O.A. (1980) Alternative synthesis of enantiomeric 1-diphenylphosphino-2-dimethylaminomethylferrocene (Kumada's ligand) Journal of Organometallic Chemistry, 202 (2) doi:10.1016/s0022-328x(00)90525-4
Sokolov, V. I. (1983) Asymmetric cyclopalladation as a tool of enantioselective synthesis. Pure and Applied Chemistry, 55 (11) 1837-1844 doi:10.1351/pac198355111837
Troitskaya, L.L., Sokolov, V.I. (1985) Asymmetric induction during carbonylation of an optically active organopalladium. A novel and versatile route to enantiomeric glycerides. Journal of Organometallic Chemistry, 285 (1) 389-393 doi:10.1016/0022-328x(85)87383-6
Troitskaya, L.L., Sokolov, V.I. (1987) Dérivés organométalliques du dimétylaminométhyl ferrocène. Journal of Organometallic Chemistry, 328 (1) 169-172 doi:10.1016/s0022-328x(00)99777-8
Troitskaya, L.L., Sokolov, V.I., Bakhmutov, V.I., Reutov, O.A., Gruselle, M., Cordier, C., Jaouen, G. (1989) Stabilisation of carbenium ions species by two different adjacent organometallic moieties: synthesis, NMR study and synthetic application. Journal of Organometallic Chemistry, 364 (1) 195-206 doi:10.1016/0022-328x(89)85343-4
Sokolov, V.I., Troitskaya, L.L., Reutov, O.A. (1969) Oxymercuration of optically active trans-cyclooctene. Journal of Organometallic Chemistry, 17 (2) 323-324 doi:10.1016/s0022-328x(00)88621-0
 
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