Preparation of 9-Membered Cyclic Ethers from Phthalans. Synthesis of Obtusan

Elliott, Mark Christopher ORCID: https://orcid.org/0000-0003-0132-0818, Moody, Christopher J. and Mowlem, Timothy J. 1993. Preparation of 9-Membered Cyclic Ethers from Phthalans. Synthesis of Obtusan. Synlett 1993 (12) , pp. 909-910. 10.1055/s-1993-22648

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Abstract

Phthalans 1-3 have been converted into oxonane-3,8-diones 7-9 by a 3-step sequence involving Birch reduction, hydrogenation and oxidative cleavage; the 2-ethyl-9-pentyl derivative 9 has been deoxygenated to give obtusan 12. The method was extended to the preparation of azonane 15 from isoindoline.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Schools > Chemistry
Subjects:	Q Science > QD Chemistry
Publisher:	Georg Thieme Verlag
ISSN:	0936-5214
Last Modified:	21 Oct 2022 10:21
URI:	https://orca.cardiff.ac.uk/id/eprint/39960

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