Search: onr:"swepub:oai:DiVA.org:uu-80012" > Total synthesis of ...
Fältnamn | Indikatorer | Metadata |
---|---|---|
000 | 01946nam a2200349 4500 | |
001 | oai:DiVA.org:uu-80012 | |
003 | SwePub | |
008 | 081017s1997 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-800122 URI |
040 | a (SwePub)uu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a vet2 swepub-contenttype |
072 | 7 | a ovr2 swepub-publicationtype |
100 | 1 | a Tanner, Du Uppsala universitet4 aut |
245 | 1 0 | a Total synthesis of balanol .2. Completion of the synthesis and investigation of the structure and reactivity of two key heterocyclic intermediates. |
264 | 1 | b PERGAMON-ELSEVIER SCIENCE LTD,c 1997 |
300 | a 4857-4868 s. | |
338 | a print2 rdacarrier | |
500 | a Addresses: Tanner D, TECH UNIV DENMARK, DEPT ORGAN CHEM, BLDG 201, DK-2800 LYNGBY, DENMARK. UNIV UPPSALA, DEPT ORGAN CHEM, S-75121 UPPSALA, SWEDEN. ASTRO DRACO AB, S-22100 LUND, SWEDEN. UNIV STOCKHOLM, ARRHENIUS LAB, S-10691 STOCKHOLM, SWEDEN. | |
520 | a A convergent enantioselective total synthesis of the natural product (-)-balanol (1) is described. In addition to benzophenone fragment 8, key intermediates are chiral bicyclic aziridine 3 and the corresponding epoxide 4, both of which undergo highly reg | |
653 | a PROTEIN-KINASE-C; SEMIEMPIRICAL METHODS; CHIRAL AZIRIDINES; PARAMETERS; EPOXIDES; OPTIMIZATION; OXAZOLINES; INHIBITOR; ANALOGS; RING | |
700 | 1 | a Tedenborg, Lu Uppsala universitet4 aut |
700 | 1 | a Almario, Au Uppsala universitet4 aut |
700 | 1 | a Pettersson, Iu Uppsala universitet4 aut |
700 | 1 | a Csoregh, Iu Uppsala universitet4 aut |
700 | 1 | a Kelly, NMu Uppsala universitet4 aut |
700 | 1 | a Andersson, PGu Uppsala universitet4 aut |
700 | 1 | a Hogberg, Tu Uppsala universitet4 aut |
710 | 2 | a Uppsala universitet4 org |
773 | 0 | t TETRAHEDRONd : PERGAMON-ELSEVIER SCIENCE LTDg 53:13q 53:13 |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-80012 |
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