Chromium and molybdenum carbonyl complexes of C7Ph7H and C7Ph5Me2H and of C7Ph7H(CO), the Diels-Alder adduct of tetracyclone and triphenylcyclopropene: Variable-temperature NMR and x-ray cr

DOI: 10.1021/om00003a015

Source and publish data:

Organometallics p. 1139 - 1151 (1995)

Update date:2022-07-30

Topics:

Authors:

Chao, Lisa C. F.

Gupta, Hari K.

Hughes, Donald W.

Britten, James F.

Rigby, Suzie S.

Bain, Alex D.

McGlinchey, Michael J.

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Article abstract of DOI:10.1021/om00003a015

The Diels-Alder reaction of tetraphenylcyclopentadienone (tetracyclone) with triphenylcyclopropene yields the adduct 2 with an endo hydrogen at C(7); thermal elimination of CO produces heptaphenylcycloheptatriene (1a). This initially formed isomer with a

Full text of DOI:10.1021/om00003a015

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