Results 171 to 180 of about 10,332 (223)
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Direct use of allylic alcohols and allylic amines in palladium-catalyzed allylic amination

Chemical Communications, 2017
Allylic alcohols and allylic amines were directly utilized in a Pd-catalyzed hydrogen-bond-activated allylic amination under mild reaction conditions in the absence of any additives. The catalytic system is compatible with a variety of functional groups and can be used to prepare a wide range of linear allylic amines in good to excellent yields.
Jiangyan Jing   +5 more
openaire   +2 more sources

Allylation of quinones by allylic indium reagents

Journal of Organometallic Chemistry, 1991
Abstract Allylation of a variety of quinones by allylic indium sesquihalides was studied. Reactions of unsubstituted p -benzoquinone with allylindium, prenylindium, and geranylindium reagents gave, after oxidation with silver oxide, the corresponding allylated quinones in good yields. These reactions appear to proceed via 1,2-addition of the allylic
Shuki Araki   +2 more
openaire   +1 more source

Palladium‐Catalyzed Allylation with Allyl Carbonates

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Marcial Moreno‐Manas, Roser Pleixats
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Cycloadditions of allyl cations, 22. Allyl alcohols as precursors of allyl cations

Chemische Berichte, 1980
AbstractAllyl alcohols such as 3‐ethoxy‐2‐methyl‐3‐buten‐2‐ol (4), the silylated alcohol 8 and also 2‐methyl‐3‐pentyn‐2‐ol (12) have been converted into the corresponding trifluoroacetates (5, 9, 13), which in the presence of zinc halide/ethyldiisopropylamine react with conjugated dienes to form bridged seven‐membered rings (14, 16, 18, 20–24) in good ...
H. M. R. Hoffmann, Jürgen Matthei
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Direct conversion of allylic nitro compounds into allyl sulphides and allyl sulphones

Journal of the Chemical Society, Chemical Communications, 1985
Allylic nitro compounds are directly converted into allyl sulphides or allyl sulphones with high regioselectivity on treatment with sodium benzenethiolate alone or with sodium benzenesulphinate in the presence of a catalytic amount of Pd(PPh3)4.
Noboru Ono   +3 more
openaire   +1 more source

Substituted Allyl Diphenylphosphine Oxides as Radical Allylating Agents

Angewandte Chemie International Edition, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Ouvry, Gilles   +2 more
openaire   +3 more sources

Solvent-Mediated Allylation of Carbonyl Compounds with Allylic Stannanes

The Journal of Organic Chemistry, 1997
Methanol promotes the addition of allyltrimethylstannane (1a) to isobutyraldehyde (2a, 30 degrees C) yielding the corresponding homoallylic alcohol (3a), without the necessity for added catalyst. The corresponding reaction of aldehydes 2a-eor activated ketone 2f with tetraallyltin (1b, 0.25 equiv) is substantially faster and proceeds in high yield (81 ...
Cokley, TM   +4 more
openaire   +4 more sources

Rearrangement of allylic sulfoximines to allylic sulfinamides

Tetrahedron Letters, 1994
Abstract Thermolysis of the enantiomerically pure allylic sulfoximines 3a,b leads to their partial rearrangement to the isomeric allylic sulfinamides 5a,b and 6a,b, respectively, with complete retention of configuration at the S-atom. Racemization of the allylic sulfoximines 3a,b at the S-atom does not occur.
Hans-Joachim Gais   +2 more
openaire   +1 more source

Allylic alcohols as synthons of allylic carbanions. Palladium-catalyzed carbonyl allylation by allylic alcohols with tin dichloride

Journal of the American Chemical Society, 1988
L'allylation des aldehydes est chimioselective et a ete effectuee en presence du groupement ...
Yoshiro. Masuyama   +2 more
openaire   +1 more source

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