Synthesis of Substituted Naphtho‐Ferrocenes via a Gold(I)‐Catalyzed Intramolecular 6‐endo‐Dig Cyclization
A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐endo‐dig cyclization strategy. The salient features of this reaction include easy operation, broad substrate scope, high yields, mild conditions and it works well in wet so...
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Published in | Chinese journal of chemistry Vol. 35; no. 6; pp. 849 - 852 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag GmbH & Co. KGaA
01.06.2017
Wiley Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | A novel series of naphtho‐ferrocene derivatives were synthesized in high yields by an efficient gold‐catalyzed intramolecular 6‐endo‐dig cyclization strategy. The salient features of this reaction include easy operation, broad substrate scope, high yields, mild conditions and it works well in wet solvent under air at room temperature.
A novel series of naphtho‐ferrocene derivatives were synthesized by a classical and efficient gold‐catalyzed intramolecular cyclization strategy. This reaction is easy to handle, with broad scope and in quantitative yield, and it works well in wet solvent under air. |
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ISSN: | 1001-604X 1614-7065 |
DOI: | 10.1002/cjoc.201600886 |