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Results 1 to 25 of 1299

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The reaction of β-(trimethylsilyl)alkyl phenyl sulfones with oxiranes. A method for stereocontrolled synthesis of homoallylic alcoholsKABAT, M. M; WICHA, J.Tetrahedron letters. 1991, Vol 32, Num 8, pp 1073-1076, issn 0040-4039, 4 p.Article

One-pot synthesis of homoallylic alcohols via a facile conversion of allylic alcohols into allylic iodidesKANAI, T; IRIFUNE, S; ISHII, Y et al.Synthesis (Stuttgart). 1989, Num 4, pp 283-286, issn 0039-7881, 4 p.Article

Enantioselective transfer aminoallylation : Synthesis of optically active homoallylic primary aminesSUGIURA, Masaharu; MORI, Chieko; KOBAYASHI, Shu et al.Journal of the American Chemical Society. 2006, Vol 128, Num 34, pp 11038-11039, issn 0002-7863, 2 p.Article

A controllable synthesis of homoallyl ketones and multiply substituted cyclopentadienes by direct insertion of aroyl cyanides to zirconacvclopentenesSHAOLIN ZHOU; BIN YAN; YUANHONG LIU et al.Journal of organic chemistry. 2005, Vol 70, Num 10, pp 4006-4012, issn 0022-3263, 7 p.Article

A facile α-iodination reaction of unsaturated amidesKITAGAWA, O; HANANO, T; HIRATA, T et al.Tetrahedron letters. 1992, Vol 33, Num 10, pp 1299-1302, issn 0040-4039Article

Synthesis of α-substituted allyl- and homoallyl-stannanes by selenoxide eliminationJEPHCOTE, V. J; THOMAS, E. J.Journal of the Chemical Society. Perkin transactions. I. 1991, Num 2, pp 429-434, issn 0300-922X, 6 p.Article

Differential use of the pyranoside ring for stereocontrolled routes to triquinanes : silphinene and silphiperfolene skeletaDICKSON, J. K; FRASER-REID, B.Journal of the Chemical Society. Chemical communications. 1990, Num 20, pp 1440-1443, issn 0022-4936, 4 p.Article

One-pot conversions of (silylmethyl)cyclopropanes to homoallylic alcohols and 1,4-diols based on haloborane-induced ring openingRYU, I; HIRAI, A; SUZUKI, H et al.Journal of organic chemistry. 1990, Vol 55, Num 5, pp 1409-1410, issn 0022-3263Article

Herstellung eines enantiomerenangereicherten Allyllithium-Derivates durch Deprotonierung unter kinetischer RacematspaltungZSCHAGE, O; SCHWARK, J.-R; HOPPE, D et al.Angewandte Chemie. 1990, Vol 102, Num 3, pp 336-337, issn 0044-8249Article

Technical procedures for the syntheses of carotenoids and related compounds from 6-oxo-isophorone : syntheses of (3R,3'R)-zeaxanthin. IWIDMER, E; SOUKUP, M; ZELL, R et al.Helvetica chimica acta. 1990, Vol 73, Num 4, pp 861-867, issn 0018-019X, 7 p.Article

The silyl modified sakurai (SMS) reaction. An efficient and versatile one-pot synthesis of homoallylic ethersMEKHALFIA, A; MARKO, I. E.Tetrahedron letters. 1991, Vol 32, Num 36, pp 4779-4782, issn 0040-4039Article

Total synthesis of pseudomonic acid CKECK, G. E; KACHENSKY, D. F; ENHOLM, E. J et al.Journal of organic chemistry. 1984, Vol 49, Num 8, pp 1462-1464, issn 0022-3263Article

Synthesis of α- and β- D,L-ribo-carbahex-2-ulofuranoseMARSCHNER, C; PENN, G; GRIENGL, H et al.Tetrahedron (Oxford. Print). 1993, Vol 49, Num 23, issn 0040-4020, VIII, 5067-5078 [13 p.]Article

A short enantiospecific synthesis of the ceroplastin nucleusSNIDER, B. B; YANG, K.Journal of organic chemistry. 1992, Vol 57, Num 13, pp 3615-3626, issn 0022-3263Article

Trimethylsilyl tetrafluoroborate. A convenient reagent for solvolysis reactionsCAPUTO, R; FERRERI, C; PALUMBO, G et al.Tetrahedron letters. 1984, Vol 25, Num 5, pp 577-578, issn 0040-4039Article

Asymmetric Synthesis of 2°-and 3°-Carbinols via B-Methallyl-10-(TMS and Ph)-9-borabicyclo[3.3.2]decanesROMAN, José G; SODERQUIST, John A.Journal of organic chemistry. 2007, Vol 72, Num 25, pp 9772-9775, issn 0022-3263, 4 p.Article

Barbier-type allylation of aldehydes mediated by antimony(III) chloride―metallic iron or antimony(III) chloride―metallic aluminiumWEI-BO WANG; LI-LAN SHI; RUO-HUI XU et al.Journal of the Chemical Society. Perkin transactions. I. 1990, Num 2, pp 424-425, issn 0300-922XArticle

Claisen rearrangement of allylic α-isocyano-esters: regioselective allylation of α-isocyanoesters at the α-carbonITO, Y; HIGUCHI, N; MURAKAMI, M et al.Tetrahedron letters. 1988, Vol 29, Num 40, pp 5151-5154, issn 0040-4039Article

Allylierung von Aldehyden unter Veretherung mit Dialkoxydichlorotitan und Allyltrimethylsilan; eine asymmetrische Variante der Sakurai-Reaktion = Allylation d'aldéhydes avec éthérification par le dialcoxydichlorotitane/allyltriméthylsilane; Variante asymétrique de la réaction Sakurai = Allylation of aldehydes with etherification by dialkoxydichlorotitanium/allyltrimethylsilane; an asymmetric variant of the Sakurai reactionIMWIKELRIED, R; SEEBACH, D.Angewandte Chemie. 1985, Vol 97, Num 9, pp 781-782, issn 0044-8249Article

Stereochemical requirements for fragmentation of homoallylic epoxy alcoholsHOLTON, R. A; KENNEDY, R. M.Tetrahedron letters. 1984, Vol 25, Num 40, pp 4455-4458, issn 0040-4039Article

An extremely mild 3-aza-Claisen reaction. II: New conditions and the rearrangement of α-heteroatom substituted amidesWALTERS, M. A; HOEM, A. B; ARCAND, H. R et al.Tetrahedron letters. 1993, Vol 34, Num 9, pp 1453-1456, issn 0040-4039Article

Remarkable differences in the reactivity of echinadiol and shiromodiol, biologically active epimeric germacrane derivativesAPPENDINO, G; TETTAMANZI, P; GARIBOLDI, P et al.Journal of the Chemical Society. Perkin transactions. I. 1990, Num 7, pp 2139-2144, issn 0300-922X, 6 p.Article

Technical procedures for the syntheses of carotenoids and related compounds from 6-oxo-isophorone : syntheses of (3R,3'R)-zeaxanthin. IISOUKUP, M; WIDMER, E; LUKAC, T et al.Helvetica chimica acta. 1990, Vol 73, Num 4, pp 868-873, issn 0018-019X, 6 p.Article

Conformational analysis in the directed hydrogenation of homoallylic alcoholsBIRTWISTLE, D. H; BROWN, J. M; HERBERT, R. H et al.Journal of the Chemical Society. Chemical communications. 1989, Num 3, pp 194-196, issn 0022-4936Article

Asymmetric synthesis of trans-2,5-disubstituted pyrrolidines from enantiopure homoallylic amines. Synthesis of pyrrolidine (-)-197BDAVIS, Franklin A; SONG, Minsoo; AUGUSTINE, Alexander et al.Journal of organic chemistry. 2006, Vol 71, Num 7, pp 2779-2786, issn 0022-3263, 8 p.Article

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