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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 6, 1976 - Issue 6
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Original Articles

Synthesis of 2-(2-Hydroxy-4-Methylphenyl)-Prop-1-Enyl Acetate via Thermal Rearrangement of 2-Methyl-2-(2-Hydroxy-4-Methylphenyl)-Oxirane

K. J. Divakar National Chemical Laboratory, Poona, 411008, India
&
A. S. Rao National Chemical Laboratory, Poona, 411008, India
Pages 423-428 | Received 17 May 1976, Published online: 06 Dec 2006

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VijayendraP. Kamat, RatnakarN. Asolkar & JanardanK. Kirtany. (1998) Synthesis of Flavans :One-Pot Synthesis of Flavans From 4-Methylcoumarins. Synthetic Communications 28:24, pages 4581-4587.
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Articles from other publishers (7)

Lei Miao, Shu-Ting Wang, Quan-Hao Wei, Ren-Fen Ma & Hua Zhang. (2024) Bioactive monoterpenoids and acetophenones from the aerial parts of Eupatorium fortunei. Phytochemistry 219, pages 113984.
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Subir Sabui, Subrata Ghosh, Debayan Sarkar & Ramanathapuram V. Venkateswaran. (2009) Expeditious synthesis of helianane and C-10 halogenated heliananes employing ring-closing metathesis. Tetrahedron Letters 50:32, pages 4683-4684.
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Kazuhiro Kobayashi, Daizo Nakamura, Kazuna Miyamoto, Osamu Morikawa & Hisatoshi Konishi. (2006) A Simple Synthesis of 4 H -1,3-Benzodioxin-2-one Derivatives by Iodocyclization of t -Butyl o -Vinylphenyl Carbonate Derivatives . Bulletin of the Chemical Society of Japan 79:3, pages 489-491.
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Frédéric Lecornué, Renée Paugam & Jean Ollivier. (2005) Strategies for the Total Asymmetric Synthesis of Heliannuols K and L: Scope and Limitations. European Journal of Organic Chemistry 2005:12, pages 2589-2598.
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Andrew J. Caruso & Julia L. Lee. (1997) A New Reaction of Bisphenol A and Preparation of Polysubstituted 9,9-Dimethylxanthenes. The Journal of Organic Chemistry 62:4, pages 1058-1063.
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Alan F. Thomas & Yvonne Bessiere. 1981. Total Synthesis of Natural Products. Total Synthesis of Natural Products 451 591 .
K. J. DIVAKAR & A. S. RAO. (2016) ChemInform Abstract: SYNTHESIS OF 2‐(2‐HYDROXY‐4‐METHYLPHENYL)PROP‐1‐ENYL ACETATE VIA THERMAL REARRANGEMENT OF 2‐METHYL‐2‐(2‐HYDROXY‐4‐METHYLPHENYL)OXIRANE. Chemischer Informationsdienst 8:2.
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