HIGHLY NUCLEOPHILIC TRIBUTYLTIN AZIDE IN OXIRANE RING CLEAVAGE LEADING TO 1,2-AZIDO ALCOHOL

DOI: 10.1016/S0040-4039(00)99346-8

Source and publish data:

Tetrahedron Letters p. 4153 - 4156 (1989)

Update date:2022-08-17

Topics:

Authors:

Saito, Seiki

Yamashita, Shuhei

Nishikawa, Toshiya

Yokoyama, Yoshie

Inaba, Masami

Moriwake, Toshio

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Article abstract of DOI:10.1016/S0040-4039(00)99346-8

Enhanced reactivity of tributyltin azide has been demonstrated in nucleophilic ring cleavage of oxiranes without solvent and promoter to give 1,2-azido alcohols in good to excellent yields.

Full text of DOI:10.1016/S0040-4039(00)99346-8

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