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Synthetic approach to stereoisomers of allylic alcohols possessing a trifluoromethyl groupKITAZUME, T; JENG TAIN LIN; YAMAZAKI, T et al.Journal of fluorine chemistry. 1989, Vol 43, Num 2, pp 177-187, issn 0022-1139, 11 p.Article

Control of diastereofacial selectivity in the epoxidation of rigid allylic ethersMANDVILLE, G; MOHAMMED AHMAR; BLOCH, R et al.Tetrahedron letters. 1993, Vol 34, Num 13, pp 2119-2122, issn 0040-4039Article

An efficient route to both enantiomers of N-(p-tolylsulfonyl)-benzenesulfonimidamide and their use for asymmetric allylic amination of olefinsTSUSHIMA, S; YAMADA, Y; ONAMI, T et al.Bulletin of the Chemical Society of Japan. 1989, Vol 62, Num 4, pp 1167-1178, issn 0009-2673, 12 p.Article

Double alkylation of α,β-unsaturated acetals: an inverse polarity approachYANAGISAWA, A; HABAUE, S; YAMAMOTO, H et al.Journal of the American Chemical Society. 1989, Vol 111, Num 1, pp 366-368, issn 0002-7863, 3 p.Article

Initiated tert-butyl hydroperoxide-loaded low-temperature autoxidation of alkenes : alternative hydroperoxide syntheses and the preparation of a complete set of reference materialsCOUTNEIDGE, J. L; BUSH, M; LAY-SEE LOH et al.Journal of the Chemical Society. Perkin transactions. I. 1992, Num 12, pp 1539-1548, issn 0300-922XArticle

Methods for the synthesis of allylsilanes. ISARKAR, T. K.Synthesis (Stuttgart). 1990, Num 11, pp 969-983, issn 0039-7881, 15 p.Article

1,3-Oxidative transpositions of allylic alcohols in organic synthesisLUZZIO, Frederick A.Tetrahedron (Oxford. Print). 2012, Vol 68, Num 27-28, issn 0040-4020, 5311, 5323-5339 [18 p.]Article

Methods for the synthesis of allylsilanes. IISARKAR, T. K.Synthesis (Stuttgart). 1990, Num 12, pp 1101-1111, issn 0039-7881, 11 p.Article

Palladium-triethylborane-triggered direct and regioselective conversion of allylic alcohols to allyl phenyl sulfonesCHANDRASEKHAR, Srivari; JAGADESHWAR, Vannada; SARITHA, Birudaraju et al.Journal of organic chemistry. 2005, Vol 70, Num 16, pp 6506-6507, issn 0022-3263, 2 p.Article

Synthesis and reactivity of allylic and propargylic trichloromethanesulfinatesBRAVERMAN, S; GRINSTEIN, D; LIOR, Z et al.Phosphorus, sulfur and silicon and the related elements (Print). 1993, Vol 74, Num 1-4, pp 443-444, issn 1042-6507Conference Paper

Convenient synthesis of isoprenoid chlorides by a direct chlorination processMIGNANI, G; GRASS, J. P; CHABARDES, P et al.Tetrahedron letters. 1992, Vol 33, Num 4, pp 495-498, issn 0040-4039Article

trans-3-n-propyl-L-proline is a highly favorable, conformationally restricted replacement for methionine in the C-terminal tetrapeptide of cholecystokinin. Stereoselective synthesis of 3-allyl- and 3-n-propyul-L-proline derivatives from 4-hydroxy-L-prolineHOLLADAY, M. W; LIN, C. W; MAY, C. S et al.Journal of medicinal chemistry (Print). 1991, Vol 34, Num 1, pp 455-457, issn 0022-2623, 3 p.Article

Studies on the periportal hepatotoxicity of allyl alcoholSASSE, D; MALY, I. P.Progress in histochemistry and cytochemistry. 1991, Vol 23, Num 1-4, pp 146-149, issn 0079-6336Article

Regio- and stereo-selective lithiation of diallyl amines: an easy entry to the trianionic intermediatesBARLUENGA, J; FOUBELO, F; GONZALEZ, R et al.Journal of the Chemical Society. Chemical communications. 1990, Num 7, pp 587-588, issn 0022-4936Article

Reactions of allylic carbonates derived from carbohydrates catalysed by palladium complexes : application to the alkylation of carbohydratesRAJAE LAKHMIRI; LHOSTE, P; BOULLANGER, P et al.Journal of chemical research. Synopses (Print). 1990, Num 10, issn 0308-2342, p. 342Article

Regio- and stereoselective synthesis of allyltrimethylsilanes via Krief-Reich elimination in β-seleno-γ-silyl alcoholsSARKAR, T. K; GHOSH, S. K; SATAPATHI, K et al.Tetrahedron (Oxford. Print). 1990, Vol 46, Num 6, pp 1885-1898, issn 0040-4020, 14 p.Article

On the stereoselectivity of reactions between α-methylbut-2-enylstannanes and aldehydesHULL, C; MORTLOCK, S. V; THOMAS, E. J et al.Tetrahedron (Oxford. Print). 1989, Vol 45, Num 4, pp 1007-1015, issn 0040-4020, 9 p.Article

Stereocontrolled construction of an ingenol prototype having a complete array of oxygenated and unsaturated centersPAQUETTE, L. A; ROSS, R. J; SPRINGER, J. P et al.Journal of the American Chemical Society. 1988, Vol 110, Num 18, pp 6192-6204, issn 0002-7863Article

In vitro activity of Tachyplesin III alone and in combination with terbinafine against clinical isolates of dermatophytesSIMONETTI, O; GANZETTI, G; KAMYSZ, E et al.Peptides (New York, NY. 1980). 2009, Vol 30, Num 10, pp 1794-1797, issn 0196-9781, 4 p.Article

Sequential hydrocarbon functionalization : Allylic C-H oxidation/vinylic C-H arylationDELCAMP, Jared H; WHITE, M. Christina.Journal of the American Chemical Society. 2006, Vol 128, Num 47, pp 15076-15077, issn 0002-7863, 2 p.Article

Diastereoselectivity of the thio-claisen rearrangement of acyclic precursors bearing a chiral centre adjacent to carbon 6DESERT, S; METZNER, P.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 47, pp 10327-10338, issn 0040-4020Article

The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre : diastereoselective protonation, epoxidation and acylation of allylsilanesFLEMING, I; LEWIS, J. J.Journal of the Chemical Society. Perkin transactions. I. 1992, Num 24, pp 3267-3275, issn 0300-922XArticle

Synthesis and relative structure of conocephalenol, a sesquiterpene alcohol isolated from the european liverwort Conocephalum conicumTORI, M; SONO, M; NAKASHIMA, K et al.Journal of the Chemical Society. Perkin transactions. I. 1991, Num 2, pp 447-450, issn 0300-922X, 4 p.Article

Intramolecular SN' cleavage of allylic ethers by enolate anionsPAQUETTE, L. A; REAGAN, J; SCHREIBER, S. L et al.Journal of the American Chemical Society. 1989, Vol 111, Num 6, pp 2331-2332, issn 0002-7863Article

Une nouvelle synthèse de peroxydes d'alkyle dissymétriques à partir d'alcools tertiaires = A new synthesis of unsymetrical dialkyl peroxides from tertiary alcoholsBOURGEOIS, M.-J; MONTAUDON, E; MAILLARD, B et al.Tetrahedron (Oxford. Print). 1993, Vol 49, Num 12, pp 2477-2484, issn 0040-4020Article

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