Zobrazeno 1 - 10
of 81
pro vyhledávání: '"M. A. Lapitskaya"'
Autor:
M. A. Lapitskaya, Kasimir K. Pivnitsky, Gennady I. Nikishin, A. V. Ignatenko, E. K. Starostin
Publikováno v:
Russian Chemical Bulletin. 50:833-837
A convenient method for the synthesis of ω- and (ω – 1)-acetylenic acids involves free-radical oxidative scission of cycloalkanones containing five-, six, or seven-membered cycles to give the corresponding ω-olefinic acids followed by brominatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::732a67ae2ca39b0c6788a6d38b7d4db2
https://doi.org/10.1023/a:1011303024847
https://doi.org/10.1023/a:1011303024847
Preparative synthesis of the Corey chiral controller for enantioselective dihydroxylation of olefins
Autor:
M. A. Lapitskaya, K. K. Pivnitsky
Publikováno v:
Russian Chemical Bulletin. 46:96-100
A five-step synthesis of both enantiomers of 1,2-di(2,4,6-trimethylbenzylamino)-1,2-diphenylethane,i.e., Corey (R,R)- and (S,S)-controllers for enantioselective dihydroxylation of olefins by osmium tetroxide, starting from α,α′-diphenylglyoxime,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b70581ec112cd674c4f4b18aad2f4e6a
https://doi.org/10.1007/bf02495355
https://doi.org/10.1007/bf02495355
Publikováno v:
ChemInform. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b51d5d396961766645b72e4bf3d19168
https://doi.org/10.1002/chin.201041208
https://doi.org/10.1002/chin.201041208
Autor:
M. A. Lapitskaya, K. K. Pivnitskii
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48962a0638cc3a587d3f20ae1ebb9934
https://doi.org/10.1002/chin.199109117
https://doi.org/10.1002/chin.199109117
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12c0523e648c894d41a3642b3e37c485
https://doi.org/10.1002/chin.199117224
https://doi.org/10.1002/chin.199117224
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55c070f44a981c5cf71b1f26a2b26072
https://doi.org/10.1002/chin.199123063
https://doi.org/10.1002/chin.199123063
Autor:
M. A. Lapitskaya, K. K. Pivnitskii
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::373c775367706c5c0bd58ec971645a7d
https://doi.org/10.1002/chin.199730036
https://doi.org/10.1002/chin.199730036
Autor:
Gennady I. Nikishin, Kasimir K. Pivnitsky, E. K. Starostin, M. A. Lapitskaya, A. V. Ignatenko
Publikováno v:
ChemInform. 31
Hex-5-ynoic acid, a multipurpose synthon, was synthesized in three steps starting from cyclohexanone by bromination-dehydrobromination of the intermediate hex-5-enoic acid.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::172af7bb05e8f0fc37d17ce0f94e4a4f
https://doi.org/10.1002/chin.200032063
https://doi.org/10.1002/chin.200032063
Publikováno v:
Liebigs Annalen der Chemie. 1991:195-200
During the pancreatin-catalyzed acetylation of the meso-diol 1 with 2,2,2-trichloroethyl acetate (2a) in tetrahydrofuran/tri-ethylamine, the enantiomeric monoacetates 3a and ent-3a are formed at nearly equal rates. ent-3a is rapidly acetylated in a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbee2903f5d2880bf1d1cb34d82125e9
https://doi.org/10.1002/jlac.199119910135
https://doi.org/10.1002/jlac.199119910135
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa3e4e2a76a46d9b54805b3462e7785e
https://doi.org/10.1002/chin.200040223
https://doi.org/10.1002/chin.200040223