SELECTIVE FORMATION OF NEW SOLVENT-DERIVED PRODUCTS FROM OZONOLYSES OF 1-ACETOXY- AND 1-CHLORO-2,3-DIPHENYLINDENE

DOI: 10.1016/0040-4039(88)85166-9

Source and publish data:

Tetrahedron Letters p. 3375 - 3378 (1988)

Update date:2022-07-30

Topics:

Authors:

McCollough, Kevin J.

Fujisaka, Tomohiro

Nojima, Masatomo

Kusabayashi, Shigekazu

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Article abstract of DOI:10.1016/0040-4039(88)85166-9

Ozonlysis of solutions of 1-acetoxy- and 1-chloro-2,3-diphenylindene in methanol at -70 deg C afford via a highly selective rearrangement of the corresponding intermediate primary ozonides, a seven-membered cyclic hemiperacetyl and isochroman derivate res

Full text of DOI:10.1016/0040-4039(88)85166-9

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