Výsledky vyhledávání - "KLOOSTERZIEL, H."

The chemistry of cycloheptatriene, part XIII : thermal fragmentation of 7-dimethylaminocycloheptatriene to benzene and dimethylaminocarbene ; preliminary communication

Autor: Borg, ter, A.P., Razenberg, E., Kloosterziel, H.

Publikováno v: Recueil des Travaux Chimiques des Pays-Bas, 85(8), 774-776. Royal Netherlands Chemical Society

cf. CA 3311c. 7-(Dimethylamino)cycloheptatriene (I) was heated and isomerized to give II and finally III. In addn. were also isolated 5-8% C6H6 and a compd. C8H8(NMe2)2 (IV), b0.3 57 Deg. The following mechanism is offered: I -> C6H6 + CHNMe2; I + CH

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https://research.tue.nl/nl/publications/d663cd43-0c76-4dcf-820f-38080144a334

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Isomerization of the bicyclo[5.1.0]octadienyl anion

Autor: Kloosterziel, H., Zwanenburg, E.

Publikováno v: Recueil des Travaux Chimiques des Pays-Bas, 88(12), 1373-1376. Royal Netherlands Chemical Society

NMR spectroscopy has revealed that the bicyclo[5.1.0]octadienyl anion (I) isomerizes by opening of the three-membered ring and a 1,2 shift of h to the 1,6-methanoheptatrienyl anion. The symmetry-forbidden electrocyclic ring opening of I to the cycloo

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https://research.tue.nl/nl/publications/7aede60a-69ba-4091-9dae-a645e2a2fdd1

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Photo-addition of trichloromethanesulfenyl chloride to carbon-carbon double bonds

Autor: Kloosterziel, H.

Publikováno v: Quarterly Reports on Sulfur Chemistry, 2(4), 353-355

The CL3CO radical in the photoaddn. of CL2CSCl to olefins isa chain-carrying radical. The structures of the adducts with styrene, propylene, allyl chloride, methallyl chloride, and allyl bromide are consistent with this conclusion, and the mechanism

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https://research.tue.nl/nl/publications/052ace2f-3d88-4d84-a2cc-53532d70fad6

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Thermal isomerizations of trimethylcyclopentadienes

Autor: Haan, de, J.W., Kloosterziel, H.

Publikováno v: Recueil des Travaux Chimiques des Pays-Bas, 84(12), 1594-1596. Royal Netherlands Chemical Society

The title reaction was studied in gas phase in a microreactor with residence times of 5-50 sec. and the products studied by their spectral data and their hydrogenation products. On heating 1,5,5-trimethylcyclopenta-1,3-diene at 350-400 Deg, it gave 1

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https://research.tue.nl/nl/publications/70c1f0a5-feaa-4453-86a6-9d59999a2795

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