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An approach to the synthesis of tricholomalide A: An effective means for achieving homo-Robinson annulation

Authors
Min, Sun-JoonDanishefsky, Samuel J.
Issue Date
May-2008
Publisher
Elsevier BV
Citation
Tetrahedron Letters, v.49, no.21, pp 3496 - 3499
Pages
4
Indexed
SCOPUS
Journal Title
Tetrahedron Letters
Volume
49
Number
21
Start Page
3496
End Page
3499
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/42454
DOI
10.1016/j.tetlet.2008.03.101
ISSN
0040-4039
Abstract
A procedure has been developed for the construction of 7,5-fused ring systems through the ring expansion of silyl enol ethers. This method has been applied to the synthesis of an intermediate en route to the natural product, tricholomalide A. (c) 2008 Elsevier Ltd. All rights reserved.
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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ERICA 공학대학 (ERICA 에너지바이오학과)
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