Synthetic studies on spiroketal natural products. IV: A stereoselective synthesis of (3S,5S,6R,9R,RS)-3-benzyloxymethyl-9-hydroxymethyl-5-(p-tolyl)sulfinyl-1,7-dioxaspiro[5.5]undecane, a key intermediate for talaromycins
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1993, Vol.41 (2), p.339-345 |
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container_title | Chemical & pharmaceutical bulletin |
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creator | IWATA, C MAEZAKI, N HATTORI, K FUJITA, M MORITANI, Y TAKEMOTO, Y TANAKA, T IMANISHI, T |
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doi_str_mv | 10.1248/cpb.41.339 |
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source | J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; EZB-FREE-00999 freely available EZB journals; Free Full-Text Journals in Chemistry |
subjects | Chemistry Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives Organic chemistry Preparations and properties |
title | Synthetic studies on spiroketal natural products. IV: A stereoselective synthesis of (3S,5S,6R,9R,RS)-3-benzyloxymethyl-9-hydroxymethyl-5-(p-tolyl)sulfinyl-1,7-dioxaspiro[5.5]undecane, a key intermediate for talaromycins |
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