Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones

Spiro[4.4]non- and spiro[4.5] dec-2-ene-1,6-diones [2; n = 0 and 1] were prepared in moderate to high enantiomeric purities via asymmetric allylation of enamines 6 and ketal derivatives 7 and 8 formed from keto-esters 5, followed by a carbanionic cyclization process. © 1994.

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Main Authors:	B. Chitkul, Y. Pinyopronpanich, C. Thebtaranonth, Y. Thebtaranonth, W. C. Taylor
Other Authors:	Mahidol University
Format:	Article
Published:	2018
Subjects:	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics
Online Access:	https://repository.li.mahidol.ac.th/handle/123456789/9517
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Institution:	Mahidol University

id	th-mahidol.9517
record_format	dspace
spelling	th-mahidol.95172018-02-27T11:29:59Z Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones B. Chitkul Y. Pinyopronpanich C. Thebtaranonth Y. Thebtaranonth W. C. Taylor Mahidol University The University of Sydney Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Spiro[4.4]non- and spiro[4.5] dec-2-ene-1,6-diones [2; n = 0 and 1] were prepared in moderate to high enantiomeric purities via asymmetric allylation of enamines 6 and ketal derivatives 7 and 8 formed from keto-esters 5, followed by a carbanionic cyclization process. © 1994. 2018-02-27T04:25:25Z 2018-02-27T04:25:25Z 1994-02-14 Article Tetrahedron Letters. Vol.35, No.7 (1994), 1099-1102 10.1016/S0040-4039(00)79975-8 00404039 2-s2.0-0028354367 https://repository.li.mahidol.ac.th/handle/123456789/9517 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028354367&origin=inward
institution	Mahidol University
building	Mahidol University Library
continent	Asia
country	Thailand Thailand
content_provider	Mahidol University Library
collection	Mahidol University Institutional Repository
topic	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics
spellingShingle	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics B. Chitkul Y. Pinyopronpanich C. Thebtaranonth Y. Thebtaranonth W. C. Taylor Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones
description	Spiro[4.4]non- and spiro[4.5] dec-2-ene-1,6-diones [2; n = 0 and 1] were prepared in moderate to high enantiomeric purities via asymmetric allylation of enamines 6 and ketal derivatives 7 and 8 formed from keto-esters 5, followed by a carbanionic cyclization process. © 1994.
author2	Mahidol University
author_facet	Mahidol University B. Chitkul Y. Pinyopronpanich C. Thebtaranonth Y. Thebtaranonth W. C. Taylor
format	Article
author	B. Chitkul Y. Pinyopronpanich C. Thebtaranonth Y. Thebtaranonth W. C. Taylor
author_sort	B. Chitkul
title	Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones
title_short	Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones
title_full	Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones
title_fullStr	Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones
title_full_unstemmed	Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones
title_sort	enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones
publishDate	2018
url	https://repository.li.mahidol.ac.th/handle/123456789/9517
_version_	1763488907192696832

Enantioselective synthesis of spiro[4.4]non- and spiro[4.5]dec-2-ene-1,6-diones

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