443308-49-4Relevant academic research and scientific papers
CLEAVABLE MULTI-ALCOHOL-BASED MICROCAPSULES
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Page/Page column 46-47, (2021/02/12)
The present invention relates to a new process for the preparation of microcapsules based on cleavable multi-alcohols. Cleavable multi-alcohol-based microcapsules are also an object of the invention. Perfuming compositions and consumer products comprising
A complex problem of diastereoisomerism: Synthesis and stereochemistry of 1,4-bis- {r-1 -AZA-c-5-ethyl-3,7-dioxabicyclo[3.3.0]octane-c-2-YL}-benzene
Maiereanu, Carmen,Toupet, Lo?c,Condamine, Eric,Silaghi-Dumitrescu, Ioan,Plé, Gérard,Ramondenc, Yvan,Dǎrǎbantu, Mircea
, p. 595 - 602 (2007/10/03)
The synthesis and the stereochemical elucidation of the title compound is described based on NMR, RX-diffractometry and ab initio theoretical calculation (level RHF/6-31G*); the verdict regarding its correct structure appears strongly dependent on the sta
Ring-chain tautomerism and other versatile behaviour of 1,4-diimino- and 1,2-phenylene derivatives of some C-substituted serinols
Maiereanu, Carmen,Darabantu, Mircea,Plé, Gérard,Berghian, Camelia,Condamine, Eric,Ramondenc, Yvan,Silaghi-Dumitrescu, Ion,Mager, Sorin
, p. 2681 - 2693 (2007/10/03)
The behaviour of the title compounds, obtained from terephthaldicarboxaldehyde or 1,2-phthaldicarboxaldehyde and certain (non)chiral C-substituted serinols is discussed in terms of ring (chain)-chain (ring) tautomerism (1,4-phenylene derivatives) or formal intramolecular redox isomerisation (1,2-derivatives).
