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Nuclear magnetic resonance spectral analysis and conformational properties of 11 -benzoyl-9,9a,10,11-tetrahydro-4H-indolo[4, 3 -ab]carbazole

Journal of pharmaceutical and biomedical analysis, 1998, Vol.16 (5), p.723-732

1998

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Potential antitumor agents. Synthesis, reactivity, and cytotoxicity of .alpha.-methylene carbonyl compounds

Journal of medicinal chemistry, 1978-08, Vol.21 (8), p.815-819

1978

Volltextzugriff (PDF)

Alkylation of aromatic compounds with pummerer rearrangement intermediates. Application to the preparation of methyl-aryl compounds

Tetrahedron letters, 1985, Vol.26 (23), p.2787-2788

Stamos, Ioannis K.

1985

Volltextzugriff (PDF)

Arylation of α-phosphoryl sulfides via their pummerer rearrangement intermediates generated from the corresponding sulfoxides

Tetrahedron letters, 1986, Vol.27 (51), p.6261-6262

Stamos, Ioannis K.

1986

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An approach to 1-alkyl-3-phenylpiperidine derivatives containing 2,5-functionalized groups: 1-methyl-2-(4-chlorophenylthiomethyl)-5-(methoxycarbonyl)- piperidine

Tetrahedron, 1994, Vol.50 (35), p.10477-10482

1994

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Potential antitumor agents. Synthesis of bifunctional .alpha.-methylene-.gamma.-butyrolactones

Journal of medicinal chemistry, 1976-02, Vol.19 (2), p.309-313

1976

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Mild reaction of Pummerer rearrangement products with aromatic compounds in the presence of Lewis acids. Application to the preparation of arylmethylene ketones22, arylacetoesters, and arylacetonitriles

Tetrahedron letters, 1985, Vol.26 (4), p.477-480

STAMOS, I. K

1985

Volltextzugriff (PDF)

Tandem rearrangement involving a β-hydroxysulfoxide and cyclization processes toward the 1-benzenesulfonyl-5-benzenethio-1,2,2a,3,4,5-hexahydrobenz[c,d]indole oxygenated at the 4-position

Journal of heterocyclic chemistry, 1997-09, Vol.34 (5), p.1487-1493

Stamos, Ioannis K.

1997

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ChemInform Abstract: Tandem Rearrangement Involving a β-Hydroxysulfoxide and Cyclization Processes Toward the 1-Benzenesulfonyl-5-benzenethio-1,2,2a,3,4,5-hexahydrobenz[c,d]indole Oxygenated at the 4-Position

ChemInform, 1998-04, Vol.29 (16), p.no-no

STAMOS, I. K.

1998

Volltextzugriff (PDF)

Mild reaction of pummerer rearrangement products with aromatic compounds in the presence of lewis acids. Application to the preparation of arylmethylene ketones, arylacetoesters, and arylacetonitriles

Tetrahedron letters, 1985, Vol.26 (4), p.477-480

Stamos, Ioannis K.

1985

Volltextzugriff (PDF)

Alkylation and arylation at the C-3′ side chain position of cephalosporins via a pummerer intermediate

Journal of heterocyclic chemistry, 1996-05, Vol.33 (3), p.987-988

1996

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A trilactone related to anemonin

Journal of heterocyclic chemistry, 1996-05, Vol.33 (3), p.1001-1002

1996

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ChemInform Abstract: Arylation of α‐Phosphoryl Sulfides via Their Pummerer Rearrangement Intermediates Generated from the Corresponding Sulfoxides

ChemInform, 1987-06, Vol.18 (26), p.no-no

STAMOS, I. K.

1987

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ChemInform Abstract: A Trilactone Related to Anemonin

ChemInform, 1996-12, Vol.27 (50), p.no-no

1996

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ChemInform Abstract: Alkylation and Arylation at the C-3′ Side Chain Position of Cephalosporins via a Pummerer Intermediate

ChemInform, 1996-12, Vol.27 (50), p.no-no

1996

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A Direct and Versatile Synthesis of 5-(2-Di-n-Propylaminoethyl)-7-methoxyindole

Synthetic communications, 1993-08, Vol.23 (16), p.2241-2249

1993

Volltextzugriff (PDF)

ChemInform Abstract: The Potential Utility of Homoacylation Through the Pummerer Rearrangement-Intermediates. A Direct Approach to the 1- Benzenesulfonyl-4-keto-8-methoxy-1,2,2a,3,4,5-hexahydrobenz(cd)indole via intra-Homoacylation

ChemInform, 1995-11, Vol.26 (45), p.no-no

1995

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ChemInform Abstract: The Utility of the Pummerer Rearrangement Intermediates in the Presence of Lewis Acids. A Short and Practical Synthesis of 4-(2-Di-n- propylaminoethyl)-7-methoxyindole (V)

ChemInform, 1994-10, Vol.25 (43), p.no-no

1994

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ChemInform Abstract: A Direct and Versatile Synthesis of 5-(2-Di-n-propylaminoethyl)-7- methoxyindole

ChemInform, 1993-12, Vol.24 (50), p.no-no

1993

Volltextzugriff (PDF)

Aldehyde-enamines from α-oxocarboxylic acids. A facile and general route to aldehydes via decarboxylation of α-oxocarboxylic acids carrying β-hydrogens

Tetrahedron letters, 1982, Vol.23 (4), p.459-462

Stamos, Ioannis K.

1982

Volltextzugriff (PDF)

Synthesis and analysis of compounds having the skeleton of ergot alkaloids with the nitrogen atom in the D-ring transposed

Journal of heterocyclic chemistry, 1995-07, Vol.32 (4), p.1303-1308

1995

Volltextzugriff (PDF)

A Convenient and Efficient Process to 5-(2-Di-n-Propylaminoethyl)-6-hydroxyindole

Synthetic communications, 1994-04, Vol.24 (8), p.1129-1136

1994

Volltextzugriff (PDF)

A Convenient Preparation of Ethyl 5,6-Dimethoxyindole-3-acetate

Synthesis (Stuttgart), 1980-01, Vol.1980 (8), p.663-664

Stamos, Ioannis K.

1980

Volltextzugriff (PDF)

ChemInform Abstract: An Approach to 1-Alkyl-3-phenylpiperidine Derivatives Containing 2,5- Functionalized Groups: 1-Methyl-2-(4-chlorophenylthiomethyl)-5-( methoxycarbonyl)piperidine

ChemInform, 1995-02, Vol.26 (8), p.no-no

1995

Volltextzugriff (PDF)

Potential antitumor agents. Synthesis, reactivity, and cytoxicity of alpha-methylene carbonyl compounds

Journal of medicinal chemistry, 1978-08, Vol.21 (8), p.815

1978

Volltextzugriff (PDF)

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Nuclear magnetic resonance spectral analysis and conformational properties of 11 -benzoyl-9,9a,10,11-tetrahydro-4H-indolo[4, 3 -ab]carbazole

Potential antitumor agents. Synthesis, reactivity, and cytotoxicity of .alpha.-methylene carbonyl compounds

Alkylation of aromatic compounds with pummerer rearrangement intermediates. Application to the preparation of methyl-aryl compounds

Arylation of α-phosphoryl sulfides via their pummerer rearrangement intermediates generated from the corresponding sulfoxides

An approach to 1-alkyl-3-phenylpiperidine derivatives containing 2,5-functionalized groups: 1-methyl-2-(4-chlorophenylthiomethyl)-5-(methoxycarbonyl)- piperidine

Potential antitumor agents. Synthesis of bifunctional .alpha.-methylene-.gamma.-butyrolactones

Mild reaction of Pummerer rearrangement products with aromatic compounds in the presence of Lewis acids. Application to the preparation of arylmethylene ketones22, arylacetoesters, and arylacetonitriles

Tandem rearrangement involving a β-hydroxysulfoxide and cyclization processes toward the 1-benzenesulfonyl-5-benzenethio-1,2,2a,3,4,5-hexahydrobenz[c,d]indole oxygenated at the 4-position

ChemInform Abstract: Tandem Rearrangement Involving a β-Hydroxysulfoxide and Cyclization Processes Toward the 1-Benzenesulfonyl-5-benzenethio-1,2,2a,3,4,5-hexahydrobenz[c,d]indole Oxygenated at the 4-Position

Mild reaction of pummerer rearrangement products with aromatic compounds in the presence of lewis acids. Application to the preparation of arylmethylene ketones, arylacetoesters, and arylacetonitriles

Alkylation and arylation at the C-3′ side chain position of cephalosporins via a pummerer intermediate

A trilactone related to anemonin

ChemInform Abstract: Arylation of α‐Phosphoryl Sulfides via Their Pummerer Rearrangement Intermediates Generated from the Corresponding Sulfoxides

ChemInform Abstract: A Trilactone Related to Anemonin

ChemInform Abstract: Alkylation and Arylation at the C-3′ Side Chain Position of Cephalosporins via a Pummerer Intermediate

A Direct and Versatile Synthesis of 5-(2-Di-n-Propylaminoethyl)-7-methoxyindole

ChemInform Abstract: The Potential Utility of Homoacylation Through the Pummerer Rearrangement-Intermediates. A Direct Approach to the 1- Benzenesulfonyl-4-keto-8-methoxy-1,2,2a,3,4,5-hexahydrobenz(cd)indole via intra-Homoacylation

ChemInform Abstract: The Utility of the Pummerer Rearrangement Intermediates in the Presence of Lewis Acids. A Short and Practical Synthesis of 4-(2-Di-n- propylaminoethyl)-7-methoxyindole (V)

ChemInform Abstract: A Direct and Versatile Synthesis of 5-(2-Di-n-propylaminoethyl)-7- methoxyindole

Aldehyde-enamines from α-oxocarboxylic acids. A facile and general route to aldehydes via decarboxylation of α-oxocarboxylic acids carrying β-hydrogens

Synthesis and analysis of compounds having the skeleton of ergot alkaloids with the nitrogen atom in the D-ring transposed

A Convenient and Efficient Process to 5-(2-Di-n-Propylaminoethyl)-6-hydroxyindole

A Convenient Preparation of Ethyl 5,6-Dimethoxyindole-3-acetate

ChemInform Abstract: An Approach to 1-Alkyl-3-phenylpiperidine Derivatives Containing 2,5- Functionalized Groups: 1-Methyl-2-(4-chlorophenylthiomethyl)-5-( methoxycarbonyl)piperidine

Potential antitumor agents. Synthesis, reactivity, and cytoxicity of alpha-methylene carbonyl compounds

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