A synthesis of (+)-nonactic acid by means of the sulfur-ylide rearrangement

DOI: 10.1016/S0040-4020(01)80580-9

Source and publish data:

Tetrahedron p. 79 - 88 (1992)

Update date:2022-08-04

Topics:

Authors:

Honda Honda

Ishige Ishige

Araki Araki

Akimoto Akimoto

Hirayama

Tsubuki Tsubuki

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Article abstract of DOI:10.1016/S0040-4020(01)80580-9

(+)-Nonactic acid (1) has been synthesized by employing a condensation of the tetrahydro-2-furanthione (9) with dimethyl α-diazomalonate in the presence of rhodium acetate as a key reaction.

Full text of DOI:10.1016/S0040-4020(01)80580-9

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