5411-71-2Relevant academic research and scientific papers
Functional norbornanyl ester derivatives, polymers and process for preparing same
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Paragraph 0234, (2013/12/04)
This invention relates to the new functional norbornanyl ester derivative and/or polymer compositions which are easily obtainable by reacting the Diels-Alder adduct of appropriate dienes and dienophiles with carboxylic acids. In particular, this invention relates to a new process for making cyclic chemical raw materials suitable for production coating, ink, adhesive, plasticizer, thermoplastic or thermosetting plastic and functional polymers.
COSMETIC OR DERMATOLOGICAL COMPOSITION COMPRISING A POLYMER BEARING JUNCTION GROUPS, AND COSMETIC TREATMENT PROCESS
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, (2010/10/03)
The present patent application relates to a cosmetic or dermatological composition comprising, in a cosmetically or dermatologically acceptable medium, a polymer comprising: (a) a polymer backbone that may be obtained by reaction: of a polyol comprising 3 to 6 hydroxyl groups;of a monocarboxylic acid containing 6 to 32 carbon atoms;of a polycarboxylic acid comprising at least two carboxylic groups COOH, and/or of a cyclic anhydride such as a polycarboxylic acid and/or of a lactone comprising at least one carboxylic group COOH; and(b) at least one junction group linked to the said polymer backbone and capable of establishing H bonds with one or more partner junction groups, each pairing of a junction group involving at least three H (hydrogen) bonds. The patent application also concerns a cosmetic treatment process using the said composition.
A total synthesis of (±)-hop ether
Lin, Ching-Han,Su, Yi-Lin,Tai, Huo-Mu
, p. 771 - 777 (2007/10/03)
A total synthesis of the iridoid monoterpene (±)-hop ether (2) is described. The Norrish I type fragmentation of bicyclo[2.2.1]heptone (5) is the key step.{A figure is presented}.
Acid-catalysed Lactonisation and Iodolactonisation of Norbornene-carboxylic Acids
Sadikun, Amirin bin,Davies, David I.
, p. 2461 - 2466 (2007/10/02)
The acid-catalysed lactonisation of 3-(norborn-5-en-2-yl)propionic acid and 4-(norborn-5-en-2-yl)butyric acid affords 3-(2-exo-hydroxynorborn-2-endo-yl)propionic acid spiro-γ-lactone and 4-(2-exo-hydroxynorborn-2-endo-yl)butyric acid spiro-δ-lactone, resp
