Allylsilanes as carbon nucleophiles in the palladium-catalyzed 1,4-oxidation of conjugated dienes

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Fältnamn	Indikatorer	Metadata
000		01573nam a2200289 4500
001		oai:DiVA.org:uu-79972
003		SwePub
008		081017s1997 \| \|\|\|\|\|\|\|\|\|\|\|000 \|\|eng\|
024	7	a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-799722 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 Castano, AMu Uppsala universitet4 aut
245	1 0	a Allylsilanes as carbon nucleophiles in the palladium-catalyzed 1,4-oxidation of conjugated dienes
264	1	b WILEY-V C H VERLAG GMBH,c 1997
300		a 482-490 s.
338		a print2 rdacarrier
500		a Addresses: UNIV UPPSALA, DEPT ORGAN CHEM, S-75121 UPPSALA, SWEDEN.
520		a Palladium-catalyzed oxidation of cyclic 1,3-dienes 3, 5, 9, 11, and 13, with an allylsilane group in the side chain, led to an intramolecular 1,4-syn-addition to the conjugated diene through a carbocyclization. Acyclic trienesilanes 7 also underwent anal
653		a allylsilanes; catalysis; cyclizations; oxidations; palladium; OPTICALLY-ACTIVE ALLYLSILANES; CROSS-COUPLING REACTION; STEREOSELECTIVE SYNTHESIS; INTRAMOLECULAR 1;4-ADDITIONS; ALLYLIC ALKYLATION; COMPLEXES; CYCLIZATION; 1;3-DIENES; STEREOCHEMISTRY; DERIV
700	1	a Persson, BAu Uppsala universitet4 aut
700	1	a Backvall, JEu Uppsala universitet4 aut
710	2	a Uppsala universitet4 org
773	0	t CHEMISTRY-A EUROPEAN JOURNALd : WILEY-V C H VERLAG GMBHg 3:3q 3:3
856	4 8	u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-79972

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