J. PLUMET's research while affiliated with Complutense University of Madrid and other places

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Publications (101)


ChemInform Abstract: A Stereoselective Synthesis of Two Epimeric Polypropionate Fragments with Four Adjacent Chiral Centers from 7-Oxanobornene Derivatives
  • Article

December 2010

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16 Reads

ChemInform

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R. MENCHACA

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J. PLUMET

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

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ChemInform Abstract: Base-Induced Bridge Cleavage of 1,5Dimethyl7-oxabicyclo(2.2.1)hept-5- ene Systems

December 2010

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17 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: The Diels-Alder Cycloaddition Reaction of Some Substituted Furans and E-1,2Bis(phenylsulfonyl)ethylene

November 2010

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7 Reads

ChemInform

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F. IRADIER

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R. M. MANAS

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[...]

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ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Total Syntheses of (.+-.)-Cyclophellitol and (1R*,6S*)-Cyclophellitol

September 2010

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15 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Regioselective, Uncatalyzed Additions of Alcohols and Carboxylic Acids to 2-Furyloxirane. Synthetic Applications.

August 2010

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4 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Osmium-Mediated Asymmetric Synthesis of Glycosyl-myo-inositols from Oxanorbornanes.

August 2010

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7 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Stereocontrolled Transformations of Cyclohexenediols Obtained from Nucleophilic Ring Opening of 7-Oxanorbornene Derivatives.

August 2010

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7 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: The Uncatalyzed Alcoholysis of Furyl-2-oxirane. A Mechanistic Study Based on Kinetic Data.

August 2010

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14 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


ChemInform Abstract: Regio- and Stereocontrolled Alkylative Ring Opening of Unsymmetrical 8- Oxabicyclo(3.2.1)octene Systems. Synthesis of Highly Substituted Hydroxycycloheptenyl Sulfones.

August 2010

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4 Reads

ChemInform

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.


Citations (6)


... It could be unequivocally excluded that the products 3 and 4 contain an arylglyoxal alkylimine in situ ( Figure 6). By contrast, the NMR spectra of 4 in [D 5 ]pyridine (Figure 2A and Additional file 1) revealed the presence of (2E)-2-(1-adamantylimino)-1-(4-fluorophenyl) ethanone, an arylglyoxal alkylimine [56,57,58]. Its formation must be induced by [D 5 ]pyridine, since 4 dissolved in CDCl 3 gave spectra (Additional file 1) typical for 1-adamantyl nitrene-containing materials. ...

Reference:

Antiviral Agents Derived from Novel 1-Adamantyl Singlet Nitrenes
The reaction of phenylglyoxal with primary aliphatic and aromatic amines. Synthesis of phenylglyoxal monoimines and some derivatives
  • Citing Article
  • August 1984

Chemischer Informationsdienst

... The 1 H and 13 C data were consistent with those reported in the literature. 28 N-Benzyl-2-(thiophen-2-yl)acetamide (17a). The title compound is known and described. ...

On the reactivity of (7-oxabicyclo[2.2.1]hept-5-en-2-ylidene)amines. Different reaction paths leading to the same final products
  • Citing Article
  • January 2001

Helvetica Chimica Acta

... Although there have been a variety of solid reducing reagents, 1 most of them prefer the reduction of a carbonyl group to that of an imino group due to the lower electrophilicity of an imino group. 2 Recently developed dibutylchlorotin hydride 3 and trichlorosilane (1) 4,5 can also reduce an imino group. The former reducing reagent is not suitable from the viewpoint of green chemistry because of its non-catalytic nature, as well as the requirement of HMPA as a ligand, while the latter liquid reagent might be useful for industrial use because of the relatively easy handling in operation and low cost. ...

Stereochemistry of imino-group reduction. Part 3. The hydride reduction of achiral benzil monoimines
  • Citing Article
  • January 1983

Chemischer Informationsdienst

... [9] It has been noticed that the configuration around the C= N double bond may have an influence on the rotational flexibility of C substituents in imines, [10] and the mutarotation of optically active benzil monoimines was explained by hindered rotation around the internal C-C bond. [11] α-Bisimines based on benzil can exist in either (E,E), (E,Z) or (Z,Z) configuration around the C=N double bonds (Figure 1). The bond-rotation barrier around the internal C-C bond should be strongly dependent on the position of the N substituent, with strongest hindrance in the (Z,Z) isomer and the lowest in the (E,E) configuration. ...

Mutarotation and isomerization of imines. Substituted N-(1-phenylethyl)-1-benzoylbenzylideneimines.
  • Citing Article
  • December 1979

Tetrahedron Letters

... 12 Considerable efforts have been made to develop synthetic methods for chiral nitro compounds. For example, the diastereoselective nitroaldol reaction with chiral aldehydes, 13 the stereoselective Michael addition reaction of nitroalkanes or nitroalkenes, 14-20 the [4+2] or [3+2] cycloaddition reaction of nitroalkenes, 21,22 and nitroolefination reactions using chiral nitroenamines 23,24 have been reported. However, the use of chiral auxiliaries is necessary in these reactions, and a catalytic method of chiral induction would be preferable. ...

Enantioselective synthesis of cyclohexene nitroaldehydes
  • Citing Article
  • December 1989

Tetrahedron Letters

... They are significant from the point of view of organic synthesis -a series of α,β-unsaturated carbonyl compounds as well as vinyl derivatives have been obtained by the functionalisation of one or both formyl groups. (Scheme 23)A number of papers155,156 have described the synthesis of various ethynyl furan derivatives substituted in positions '2' and '5'. FDC, according to authors is the best starting material for this purpose. ...

Synthesis of 2,5-bis-(Ethynyl) furan Derivatives from 2,5-Furandicarboxaldehyde
  • Citing Article
  • May 1991

Synthetic Communications