ORGANIC SYNTHESES VIA TRANSITION-METAL COMPLEXES - 96 - 1-AZACYCLOALKENE AND 2-AZABICYCLOALKENE DERIVATIVES OF 4-AMINO-1-METALLA-1,3-DIENESBY REACTION OF SATURATED LACTIMS WITH (1-ALKYNYL)CARBENE COMPLEXES OFCHROMIUM AND TUNGSTEN
R. Aumann et al., ORGANIC SYNTHESES VIA TRANSITION-METAL COMPLEXES - 96 - 1-AZACYCLOALKENE AND 2-AZABICYCLOALKENE DERIVATIVES OF 4-AMINO-1-METALLA-1,3-DIENESBY REACTION OF SATURATED LACTIMS WITH (1-ALKYNYL)CARBENE COMPLEXES OFCHROMIUM AND TUNGSTEN, Organometallics, 17(13), 1998, pp. 2897-2905
Reaction of five- and six-membered O-alkyl lactims similar to(CH2)(n)-
N=C(OR)similar to 5 (n = 3) and 7 (n = 4) with (1-alkynyl)carbene comp
lexes (CO)(5)M=C(OEt)C=CPh 1 (a, M = Cr; b, W) gives binuclear 1-alkox
y-2-azabicyclo[n.2.0]alkene derivatives (E)-6 and (E)-8, respectively,
in 90-94% yields. Reaction of seven- and eight-membered O-alkyl lacti
ms similar to(CH2)(n)-N=C(OR)similar to 9 (n = 5) and 11 (n = 6) with
compounds 1 affords mononuclear 4-(1-aza-cyclo-2-alken-1-yl) 1-metalla
-1,3-butadienes (E)-10 and (E)-11, respectively, but no binuclear deri
vatives, Both mono- and binuclear metal compounds undergo fast transfo
rmations on contact with silica gel. Chromatography of the binuclear t
ungsten compound (E)-6b on silica gel results in fragmentation of the
(cyclobutenyl)carbene unit to give 1,11-bis(tungsta)-5-azaundeca-1,3,6
,8,-10-pentaene (13) as well as in hydrolysis of the 2-alkoxy pyrrolid
ine unit with formation of a bis(carbene) derivative 15 of an amino ac
id. Compound 13, on extended contact with silica gel, undergoes cycliz
ation and subsequent hydrolysis to 2-azabicyclo[3.3.0]octenone 14, The
rmal fragmentation of the mononuclear dihydroazepine compound (E)-10c
affords dihydro- and tetrahydropyrrolo[1,2a]azepines 17 and 18, respec
tively, X-ray crystal structural data are reported for the binuclear c
ompound (E)-6b as well as for mononuclear compounds (E)-10c and 14.