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1.
J Am Chem Soc ; 136(29): 10274-6, 2014 Jul 23.
Article in English | MEDLINE | ID: mdl-25003871

ABSTRACT

The first total synthesis of (-)-crinipellin A is described. The tetraquinane core skeleton of crinipellin A was assembled through the tandem [2 + 3] cycloaddition reaction of an allenyl diazo substrate containing a cyclopentane ring in a single operation. The absolute stereochemistry was confirmed through the total synthesis.


Subject(s)
Cyclopentanes/chemistry , Diterpenes/chemical synthesis , Methane/analogs & derivatives , Azo Compounds/chemistry , Cycloaddition Reaction , Diterpenes/chemistry , Methane/chemistry , Molecular Conformation , Stereoisomerism
2.
Chem Asian J ; 7(10): 2450-6, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22807414

ABSTRACT

Total synthesis of ceratopicanol (1) was achieved with a tandem cycloaddition reaction of allenyl diazo compound 6 via a trimethylenemethane (TMM) diyl intermediate. The TMM diyl mediated [2+3] cycloaddition reaction furnished the consecutive quaternary carbon centers and showed an unusual diastereoselectivity.


Subject(s)
Polycyclic Compounds/chemical synthesis , Azo Compounds/chemistry , Cycloaddition Reaction , Methane/analogs & derivatives , Methane/chemistry , Polycyclic Compounds/chemistry , Stereoisomerism
3.
J Am Chem Soc ; 133(45): 18050-3, 2011 Nov 16.
Article in English | MEDLINE | ID: mdl-21999462

ABSTRACT

A tandem reaction strategy for forming triquinanes from linear allenyl diazo compounds through an intramolecular 1,3-dipolar cycloaddition reaction of an allenyl diazo group that generates a trimethylenemethane (TMM) diyl followed by an intramolecular [2 + 3] TMM diyl cycloaddition reaction has been developed. The new tandem cycloaddition reaction is readily applicable to the synthesis of complex molecules with high versatility and efficiency.


Subject(s)
Azo Compounds/chemistry , Bridged-Ring Compounds/chemical synthesis , Methane/analogs & derivatives , Sesquiterpenes/chemical synthesis , Bridged-Ring Compounds/chemistry , Cyclization , Methane/chemistry , Molecular Structure , Sesquiterpenes/chemistry , Stereoisomerism
5.
Bioorg Med Chem Lett ; 18(16): 4670-4, 2008 Aug 15.
Article in English | MEDLINE | ID: mdl-18656350

ABSTRACT

A series of Incentrom A analogs that inhibit the chromosome segregation process in yeast were synthesized and tested for their effects on chromosome stability and cell proliferation. Pharmacophore and structure-activity relationship of Incentrom A for the anti-yeast activity were established.


Subject(s)
Carbazoles/chemical synthesis , Chemistry, Pharmaceutical/methods , Chromosome Segregation/drug effects , Piperazines/chemical synthesis , Antifungal Agents/pharmacology , Carbazoles/pharmacology , Cell Proliferation/drug effects , Chromosomal Instability , Drug Design , Mitosis , Models, Chemical , Molecular Structure , Piperazines/pharmacology , Saccharomyces cerevisiae/metabolism , Structure-Activity Relationship
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