Zobrazeno 1 - 10
of 74
pro vyhledávání: '"U, Lerch"'
Publikováno v:
ChemInform. 24
Racemic and optically pure 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids and esters were prepared, via base-catalyzed cyclization of 1,2-bis(halomethyl)benzenes 1a or b with diethyl 2-(acetylamino)malonate (2), subsequent decarboxylation and amid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::176437dc21a935819b5db613aa615716
https://doi.org/10.1002/chin.199334184
https://doi.org/10.1002/chin.199334184
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::294f77d1db2469a9eef546ac32fc2d65
https://doi.org/10.1002/chin.199409061
https://doi.org/10.1002/chin.199409061
Autor:
H W, Kleemann, H, Heitsch, R, Henning, W, Kramer, W, Kocher, U, Lerch, W, Linz, W U, Nickel, D, Ruppert, H, Urbach
Publikováno v:
Journal of Medicinal Chemistry. 35:559-567
Incorporation of a C-terminal pentahydroxy functionality led to potent, low molecular weight hydrophilic renin inhibitors lacking the P1' side chain. As these compounds are easy to synthesize and have sufficient water solubility, they were chosen for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ac95e4e94ac6159a771fcd182ad970
https://doi.org/10.1021/jm00081a019
https://doi.org/10.1021/jm00081a019
Publikováno v:
Synthesis. 1992:1157-1160
Racemic and optically pure 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids and esters were prepared, via base-catalyzed cyclization of 1,2-bis(halomethyl)benzenes 1a or b with diethyl 2-(acetylamino)malonate (2), subsequent decarboxylation and amid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82081b752d7f99bc37ae95581e691a4f
https://doi.org/10.1055/s-1992-26325
https://doi.org/10.1055/s-1992-26325
Autor:
Berman P, M Moffatt, Burnett D, O'Sullivan T, L Dierks, M Mantyranta, Rathwell T, MacDonald S, U Lerch, M von der Leyen
Publikováno v:
Journal of Medical Internet Research
INTRODUCTION: In 1998, the unique and experimental "Looking over the horizon - An Internet-based International Course in Comparative Healthcare Management" started. The course is a component of the larger project on "Promoting International Co-operat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d31efe12a25a8e241445c2eaa9dfd53
https://doi.org/10.2196/jmir.1.suppl1.e49
https://doi.org/10.2196/jmir.1.suppl1.e49
Publikováno v:
Tetrahedron Letters. 17:3879-3882
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6fcf2c492a007f4b1f46f5db22a5455
https://doi.org/10.1016/0040-4039(76)80172-4
https://doi.org/10.1016/0040-4039(76)80172-4
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 44:1481-1484
(I) cristallise dans P2 1 /c avec affinement jusqu'a 0,116. (II) cristallise dans Pbca avec affinement jusqu'a 0,081. La partie centrale de la molecule(I) consiste en trois heterocycles a 5 chainons. Le cycle contenant P est ferme par l'intermediaire
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e54b8a5943f54d214d0a36860b912b67
https://doi.org/10.1107/s0108270188004561
https://doi.org/10.1107/s0108270188004561
Publikováno v:
Prostaglandins. 20:153-169
Utilizing Corey's synthesis, a variety of prostaglandins (PGs) with a modified omega-side chain were prepared. The 16, 16-dimethyl-oxa-alkyl analogues of PGA2 had potent antihypertensive activity. HR 466 (16, 16-dimethyl-18-oxa-PGA2), the best compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eccf2bede638e0c042ecea72f5ac8f2c
https://doi.org/10.1016/0090-6980(80)90015-5
https://doi.org/10.1016/0090-6980(80)90015-5
Publikováno v:
Tetrahedron Letters. 18:2563-2566
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bb8ec1f165853c556980c33d62aa886
https://doi.org/10.1016/s0040-4039(01)83820-x
https://doi.org/10.1016/s0040-4039(01)83820-x
Publikováno v:
Tetrahedron Letters. 15:2441-2444
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a99610d49dadb28158648737e2432d1b
https://doi.org/10.1016/s0040-4039(01)92281-6
https://doi.org/10.1016/s0040-4039(01)92281-6