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August 4, 1997Angewandte Chemie International Edition in English

Isolation of the Quinone Mono O,S‐Acetal Intermediates of the Aromatic Pummerer‐Type Rearrangement of p‐Sulfinylphenols with 1‐Ethoxyvinyl Esters

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Authors

YKYasuyuki KitaRitsumeikan UniversityYTYoshifumi TekedaThe University of OsakaMMMasato MatsugiMeijo University

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Cite This Study

Kita et al. (1997) studied this question.

synapsesocial.com/papers/6a7fe92d563aa6d712a286fbhttps://doi.org/10.1002/anie.199715291
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Also Consider

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  1. 1Pummerer-type Cyclization of Arnstein Tripeptide Analogs Induced by O-Silylated Ketene Acetals: Studies of Penicillin Biosynthesis1994 · 26 citations
  2. 2Dienone intermediates in the Pummerer rearrangement of 4-methylsulfinyl-3,5-xylenol1978 · 11 citations
  3. 3Oxidative Intramolecular [4+2]Cycloaddition of o-[(ω-Phenylthioethynyl)acyl]phenols Followed by the Aromatic Pummerer-type Reaction: A Novel Preparation of the peri-Hydroxy Dihydroquinone Structure1997 · 12 citations
  4. 4An efficient synthesis of p-quinones utilizing a novel Pummerer-type rearrangement of p-sulfinylphenols1995 · 17 citations
  5. 5Asymmetric Pummerer-Type Reactions Induced by O-Silylated Ketene Acetals1996 · 35 citations