Tetrahydro-4H-pyran-4-one: From the Laboratory Scale to Pilot Plant Manufacture

[1]  O. Crosby.  transesterification , 2020, Catalysis from A to Z.

[2]  Xinquan Hu,et al.  Improved Synthetic Process of Dimethyl 4-Oxo-4H-pyran-3,5-dicarboxylate , 2019, Organic Process Research & Development.

[3]  F. Schiet,et al.  The Prins Reaction in the Fragrance Industry: 100th Anniversary (1919-2019). , 2019, Angewandte Chemie.

[4]  D. Snodin.  Elusive Impurities—Evidence versus Hypothesis. Technical and Regulatory Update on Alkyl Sulfonates in Sulfonic Acid Salts , 2019, Organic Process Research & Development.

[5]  S. Kim,et al.  Pharmacological use of a novel scaffold, anomeric N,N-diarylamino tetrahydropyran: molecular similarity search, chemocentric target profiling, and experimental evidence , 2017, Scientific Reports.

[6]  T. Straub,et al.  A rapid and convenient oxidation of secondary alcohols , 2017 .

[7]  Ke Chen,et al.  Scalable and Sustainable Electrochemical Allylic C–H Oxidation , 2016, Nature.

[8]  Hai Dong,et al.  Zemplén transesterification: a name reaction that has misled us for 90 years , 2015 .

[9]  M. Lemaire,et al.  Synthesis of 3‐Substituted Tetrahydrofuran and 4‐Substituted Tetrahydropyran Derivatives by Cyclization of Dicarboxylic Acids with InBr3/TMDS , 2012 .

[10]  D. Ripin,et al.  Large-scale oxidations in the pharmaceutical industry. , 2006, Chemical reviews.

[11]  S. Laschat,et al.  Concise Two-Step Synthesis of γ-Pyrone from Acetone , 2004 .

[12]  G. A. Hiegel,et al.  The Oxidation of Secondary Alcohols to Ketones with Trichloroisocyanuric Acid , 1992 .

[13]  O. Possel,et al.  Tosylmethyl isocyanide employed in a novel synthesis of ketones. A new masked formaldehyde reagent , 1977 .

[14]  C. Reese,et al.  A convenient preparation of tetrahydro-4H-pyran-4-one , 1970 .