A SYNTHESIS OF 2-EXO-SUBSTITUTED 2-ENDO-AMINONORBORNENES: ORGANOALUMINUM-PROMOTED NUCLEOPHILIC SUBSTITUTION ON 2-ENDO-ACETAMIDO-2-EXO-METHOXYNORBORNENE

DOI: 10.1016/S0040-4039(00)98067-5

Source and publish data:

Tetrahedron Letters p. 5345 - 5346 (1990)

Update date:2022-08-15

Topics: Nucleophilic substitution Norbornene Organometallic chemistry Acetamido

Authors:

Yamazaki, Hiroyoshi

Horikawa, Hiroshi

Nishitani, Takashi

Iwasaki, Tameo

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Article abstract of DOI:10.1016/S0040-4039(00)98067-5

A variety of 2-exo-substituted 2-endo-acetamidonorbornenes (2a-g) were synthesized in exceedingly high exo selectivities by organoaluminum-promoted nucleophilic substitution on 2-endo-acetamido-2-exo-methoxynorbornene.

Full text of DOI:10.1016/S0040-4039(00)98067-5

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