Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Meyer Sletzinger"'
Publikováno v:
Synthesis. 1973:50-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f233ef95838144cd27bdd386eb46949b
https://doi.org/10.1055/s-1973-22134
https://doi.org/10.1055/s-1973-22134
Autor:
William C. Lumma, G. S. Brenner, Leonard M. Weinstock, A. M. Hoinowski, Meyer Sletzinger, F. E. Roberts, Ta-Jyh Lee, Sandor Karady
Publikováno v:
Tetrahedron Letters. 16:3979-3982
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a1f650c3a3d78bdbe1ca6ed2997f7d2
https://doi.org/10.1016/s0040-4039(00)91214-0
https://doi.org/10.1016/s0040-4039(00)91214-0
Autor:
Alan W. Douglas, Meyer Sletzinger, Erwin F. Schoenewaldt, Edward J. J. Grabowski, Ulf H. Dolling, Paul Sohar
Publikováno v:
The Journal of Organic Chemistry. 43:1634-1640
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62d41b02d6b421adcd01dee66318d912
https://doi.org/10.1021/jo00403a002
https://doi.org/10.1021/jo00403a002
A facile transformation of bicyclic keto esters to bisprotected (±)-8-epithienamycin enol activation
Publikováno v:
Tetrahedron Letters. 21:4221-4224
A facile “one-pot” transformation of bicyclic keto ester (2) to bisprotected (±)-8-epithienamycin via enol phosphate activation followed by the addition-elimination reaction of N -protected cysteamine derivative is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74b359122e8c12b228cf7decaeb07723
https://doi.org/10.1016/s0040-4039(00)92867-3
https://doi.org/10.1016/s0040-4039(00)92867-3
Autor:
Meyer Sletzinger, F. E. Roberts, Sandor Karady, J. ten Broeke, Richard F. Shuman, Leonard M. Weinstock, A. M. Hoinowski, Seemon H. Pines
Publikováno v:
Tetrahedron Letters. 17:2401-2404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed05766cd8d57651a21fb52e4716093b
https://doi.org/10.1016/0040-4039(76)90003-4
https://doi.org/10.1016/0040-4039(76)90003-4
Publikováno v:
Tetrahedron Letters. 15:2625-2628
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17e8c5299f01abd564bb87e2e9224237
https://doi.org/10.1016/s0040-4039(01)92310-x
https://doi.org/10.1016/s0040-4039(01)92310-x
Publikováno v:
Tetrahedron Letters. 23:4903-4906
A convenient direct transformation of p -nitrobenzyl 6-(1′-hydroxyethyl)-1-azabicyclo-(3.2.0)heptane-3,7-dione-2-carboxylate to N -formimidoyl thienamycin utilizing the silylated derivative of N -formimidoyl cysteamine is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be04d73060b0698da37d11f36884d88e
https://doi.org/10.1016/s0040-4039(00)85743-3
https://doi.org/10.1016/s0040-4039(00)85743-3
Publikováno v:
Tetrahedron Letters. 23:4899-4902
A convenient synthesis of 3-(1′-hydroxyethyl)-2-azetidinone-4-yl acetic acid, one of the key intermediates in the thienamycin total synthesis, based on the chemistry of the dianion derived from readily available 2-azetidinone-4-yl acetic acid is de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed157f576da28946fa7e8c06a1b40ee7
https://doi.org/10.1016/s0040-4039(00)85742-1
https://doi.org/10.1016/s0040-4039(00)85742-1
Publikováno v:
The Journal of Organic Chemistry. 51:1498-1504
Synthese de l'ester methyle-1 de l'acide amino-2 hydroxy-4 pentanedicarboxylique-1,3 (precurseur de la (+) thienamycine)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::387289124e107b1774e13311edaf2b3a
https://doi.org/10.1021/jo00359a021
https://doi.org/10.1021/jo00359a021
Autor:
Ralph P. Volante, Edward G. Corley, T.M.H. Liu, Meyer Sletzinger, James M. McNamara, Thomas R. Verhoeven
Publikováno v:
Tetrahedron Letters. 26:2951-2954
The coupling of acyl anion equivalent 12b with chiral synthon 14 , derived from isoascorbic acid, and a highly stereospecific reduction of the resulting β-hydroxy ketone 3 highlight an efficient synthesis of β-hydroxy-δ-lactone 2 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7263f2aec9fb3887909e74d38a8f814b
https://doi.org/10.1016/s0040-4039(00)98589-7
https://doi.org/10.1016/s0040-4039(00)98589-7