- Vinyltin acetals in terpenic and nor-terpenic synthesis
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Vinyltin acetals obtained by stannylmetallation of homopropargyl acetals with Bu3SnMgMe/CuCN (E configuration) or by titanation of the corresponding alkyltin acetals (Z configuration) have been proved to be efficient storable precursors for the stereoselective synthesis of terpenoids, under mild experimental conditions.Due to the presence of a nucleophilic centre (Csp2-Sn bond) and of a protected electrophilic centre, they are also useful intermediates for an iterative synthesis of retinal and nor-retinoids. - Keywords: vinyltin; acetal; vinyllithium; monoterpenoid; retinal; nor-retinoid
- Launay, Valerie,Beaudet, Isabelle,Quintard, Jean-Paul
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p. 937 - 946
(2007/10/03)
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- Mechanism for the Two-bond Isomerization in the Photoirradiation of 7,9-Di-cis-retinal
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The two-bond isomerization process of 7,9-di-cis-retinal to all-trans-retinal has been shown to proceed by way of an adiabatic, stepwise process.
- Liu, Robert S. H.,Zhu, Yun
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p. 1765 - 1766
(2007/10/02)
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- Retinal, derivatives and their therapeutic use
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Therapeutic as well as preventive measures to improve cosmetic conditions and to alleviate the symptoms of dermatologic disorders with retinal and its derivatives is disclosed. Cosmetic conditions and dermatologic disorders in humans and domestic animals in which retinal and its derivatives may be useful include age spots, wrinkles, warts, eczema, seborrheic keratoses, acne, oily skin, psoriasis, dandruff, xerosis, inflammatory and pruritic skin, disturbed keratinization skin changes associated with aging and possibly viral infections. Retinal and its derivatives include their stereoisomers, for example, all-trans, 13-cis, 11-cis, 9-cis, 7-cis, 11,13-cis and 9,13-cis vitamin A aldehydes, their hydrate, hemiacetal and acetal forms, and their adduct compounds. Compositions containing retinal or its derivative may be administered systemically such as orally, or topically to the affected areas of the skin.
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- A new prenylation method using the lithium enolate of prenal. Reaction with polyunsaturated aldehydes. A short access to retinal
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The enolate of prenal 1 prepared from the corresponding silyl enol ether 2 or enol acetate 3 led to a γ-regiospecific reaction with polyunsaturated aldehydes 4 yielding dihydropyrans 5 leading after hydrolysis to polyenals 7. This process allows the introduction of the isoprenyl skeleton. A synthesis of retinal, from β-ionylidenacetaldehyde is reported.
- Duhamel, Lucette,Guillemont, Jerome,Poirier, Jean-Marie,Chabardes, Pierre
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p. 4499 - 4500
(2007/10/02)
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- Photoisomerization of Hindered Poly-cis Isomers of Retinal. Regioselectivity And One -Photon-Multiple-Bond Isomerization.
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Direct irradiation of five dicis (7,9, 7,11, 7,13, 9,11 and 9,13) and one tricis (7,9,11) isomers of retinal led to regioselective isomerization at the 13,14 bond as well as multiple-bond isomerization.
- Ganapathy, Srinivasan,Liu, Robert S. H.
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p. 6957 - 6960
(2007/10/02)
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- Transient Phenomena in the Pulse Radiolysis of Retinyl Polyenes. 1. Radical Anions
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The spectra and kinetics of formation and decay of radical anions of a number of retinyl polyenes have been studied in methanol and 2-propanol at room temperature, using pulse radiolysis and kinetic spectrophotometry.The bimolecular rate constants for the attachment of solvated electrons, e-MeOH, to the retinyl polyenes are in the diffusion-controlled limit (8.6 x 109-1.6 x 1010 M-1 s-1).The radical anions of retinol and retinol acetate have their spectral maxima at 370-390 nm, and undergo decay very slowly with second-order kinetics.On the other hand, the radical anions of retinal, retinal n-butylamine Schiff base, and retinoic acid/ester have spectral maxima at 430-510 nm, and decay by first-order kinetics in methanol with rate constants in the range 1 x 104-1 x 106 s-1.The decay rates of radical anions of retinal and retinoic acid/ester become considerably longer on going from methanol to less acidic alcohol, 2-propanol, suggesting that protonation by solvent is the major mode of their decay in protic media.In the case of retinal Schiff base, an additional slow process with bimolecular rate constant 9.0 x 107 M-1 s-1 im methanol is observed for the formation of radical anion and is ascribed to the electron-transfer reaction from the methanol radical, .CH2OH.
- Raghavan, N.V.,Das, P.K.,Bobrowski, K.
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p. 4569 - 4573
(2007/10/02)
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