Zobrazeno 1 - 10
of 66
pro vyhledávání: '"M. S. Ermolenko"'
Autor:
I. N. Gaisina, Z. A. Yusupov, M. S. Ermolenko, Mansur S. Miftakhov, R. R. Muslukhov, N. K. Selezneva, O. M. Kuznetsov
Publikováno v:
Russian Chemical Bulletin. 50:1101-1106
Alkylation of (1R,2R,5R)-2-benzenesulfonyl-6,8-dioxa-bicyclo[3.2.1]octan-3-one, which is accessible from levoglucosan, afforded (1R,2R,5R)-2-benzenesylfonyl-2,4,4-trimethyl-6,8-dioxabicyclo[3.2.1]octan-3-one. This was further converted into (1S,2R,3S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec8259aab3d3d2394360cc1c19663468
https://doi.org/10.1023/a:1011350225873
https://doi.org/10.1023/a:1011350225873
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84730b30569e8d98e0500f59f4815e31
https://doi.org/10.1002/chin.199124247
https://doi.org/10.1002/chin.199124247
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e51316ae48c22cb25e412c889f16fb80
https://doi.org/10.1002/chin.199124248
https://doi.org/10.1002/chin.199124248
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b2819115ce70999cbb3f6d96e606cb9
https://doi.org/10.1002/chin.199424276
https://doi.org/10.1002/chin.199424276
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::335e1cc77b0bb2073fdd7ea5040662a6
https://doi.org/10.1002/chin.199531198
https://doi.org/10.1002/chin.199531198
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34bfce7e5be9ab583787c9f825f8614b
https://doi.org/10.1002/chin.199531197
https://doi.org/10.1002/chin.199531197
Autor:
Z. A. Yusupov, R. R. Muslukhov, O. M. Kuznetsov, N. K. Selezneva, M. S. Ermolenko, Mansur S. Miftakhov, I. N. Gaisina
Publikováno v:
ChemInform. 33
Alkylation of (1R,2R,5R)-2-benzenesulfonyl-6,8-dioxa-bicyclo[3.2.1]octan-3-one, which is accessible from levoglucosan, afforded (1R,2R,5R)-2-benzenesylfonyl-2,4,4-trimethyl-6,8-dioxabicyclo[3.2.1]octan-3-one. This was further converted into (1S,2R,3S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1dff9f88083fd61635117e998b36a34
https://doi.org/10.1002/chin.200207208
https://doi.org/10.1002/chin.200207208
Publikováno v:
Tetrahedron. 47:2317-2336
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::550d4380ae202127906e339e5bcb4c6e
https://doi.org/10.1016/s0040-4020(01)96140-x
https://doi.org/10.1016/s0040-4020(01)96140-x
Publikováno v:
Tetrahedron. 47:2291-2316
An approach to the synthesis of aglycones of macrolide antibiotics erythromycine A and B is discussed and preparation of common C1-C10 and C1-C13 segments starting from levoglucosane is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70ad8a98405ab9af81eb10992ace82dd
https://doi.org/10.1016/s0040-4020(01)96139-3
https://doi.org/10.1016/s0040-4020(01)96139-3
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 39:179-183
A complete, stereocontrolled synthesis for erythronolide A was carried out by fusion of the (C9-C13)+(C7-C8)+(C1-C6) fragments from levoglucosan in 61 steps with 0.28% total yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d3ce4cb34134327d59a9bd21c812d75
https://doi.org/10.1007/bf00963026
https://doi.org/10.1007/bf00963026