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ChemInform Abstract: Peroxido Complexes of Vanadium(V) as Ligands. Crystal Structures of [Cd(NH3)6] [{VO(O2)2(OH)}2{μ-Cd (NH3)4}] and [{VO(O2)2(Im)}2{μ-Cu(Im)4}] (Im = Imidazole)

ChemInform, 2014-07, Vol.45 (29), p.no-no

2014

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HPLC Separation of Amino Acid Enantiomers and Small Peptides on Macrocyclic Antibiotic Based Chiral Stationary Phases

ChemInform, 2007-07, Vol.38 (31), p.no-no

2007

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One-Pot Synthesis of N-Protected β-Chiral Amino Alcohols

ChemInform, 2003-09, Vol.34 (37), p.no-no

2003

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4-Amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic Acid (β-TOAC), the First Spin-Labeled, Cyclic, Chiral β-Amino Acid Resolved in an Enantiomerically Pure State

ChemInform, 2003-08, Vol.34 (31), p.no-no

2003

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ChemInform Abstract: Convenient Synthesis of 3,4-Methano-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acid (VIII) and Its Derivatives (VII) as Doubly Constrained Nonproteinogenic Amino Acid Derivatives

ChemInform, 2000-12, Vol.31 (50), p.no-no

2000

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ChemInform Abstract: Ring Transformations of β-Lactam-Condensed 1,3-Benzothiazines to Isoquinoline and Thiazole Derivatives by Sulfur Extrusion and Addition Sequences

ChemInform, 2012-12, Vol.43 (51), p.no-no

2012

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ChemInform Abstract: Ring Transformations of [beta]-Lactam-Condensed 1,3-Benzothiazines to Isoquinoline and Thiazole Derivatives by Sulfur Extrusion and Addition Sequences

ChemInform, 2012-12, Vol.43 (51), p.no

2012

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ChemInform Abstract: One-Step Ring-Closure Procedure for 4,5-Dihydro-1,3-thiazino[5,4-b]indole Derivatives with Lawesson′s Reagent. The Fifth Dihydro-1,3-thiazino[b]indole Isomer

ChemInform, 2012-02, Vol.43 (6), p.no-no

2012

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ChemInform Abstract: One-Step Ring-Closure Procedure for 4,5-Dihydro-1,3-thiazino[5,4-b]indole Derivatives with Lawesson's Reagent. The Fifth Dihydro-1,3-thiazino[b]indole Isomer

ChemInform, 2012-02, Vol.43 (6), p.no

2012

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ChemInform Abstract: A Convenient Synthesis of 1,4-Benzothiazepines from 1,3-Benzothiazines via the Ring Transformation of β-Lactam-Condensed 1,3-Benzothiazine Derivatives

ChemInform, 2011-01, Vol.42 (1), p.no-no

2011

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ChemInform Abstract: Unexpected Formation of Indenoisoquinoline Derivatives from Thia Analogues of Protoberberine Alkaloids

ChemInform, 2012-12, Vol.43 (50), p.no-no

2012

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ChemInform Abstract: Staudinger and retro-Staudinger Reactions. The Dichloro-β-lactam Moiety as a Useful Handle for the Synthesis of 4-Aryl-2H-1,3-benzothiazine 1,2-Dioxides

ChemInform, 2010-10, Vol.41 (40), p.no-no

2010

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ChemInform Abstract: Expected and Unexpected Reactions of 1,3-Benzothiazine Derivatives. Part 2. Formation of Isomeric 5,6-Dihydro-1,5-benzothiazocines

ChemInform, 2011-05, Vol.42 (20), p.no-no

2011

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ChemInform Abstract: Expected and Unexpected Reactions of 1,3-Benzothiazine Derivatives. Part 1. Ring Transformation of β-Lactam-Condensed 1,3-Benzothiazines into 4,5-Dihydro-1,4-benzothiazepines and Indolo-1,4-benzothiazepines

ChemInform, 2011-04, Vol.42 (15), p.no-no

2011

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Biosynthetic Capacities of Actinomycetes. Part 36. Fogacin (I), a Novel Cyclic Octaketide Produced by Streptomyces Strain T 6319

ChemInform, 2006-11, Vol.37 (48), p.no-no

2006

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Biosynthetic Capacities of Actinomycetes. Part 32. Retymicin (I), Galtamycin B (II), Saquayamycin Z and Ribofuranosyllumichrome (III), Novel Secondary Metabolites from Micromonospora sp. Tue 6368. Part 1. Taxonomy, Fermentation, Isolation and Biological Activities

ChemInform, 2005-09, Vol.36 (36), p.no-no

2005

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Retymicin, Galtamycin B, Saquayamycin Z and Ribofuranosyllumichrome, Novel Secondary Metabolites from Micromonospora sp. Tue 6368. Part 2. Structure Elucidation

ChemInform, 2005-07, Vol.36 (27), p.no-no

2005

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ChemInform Abstract: High-Pressure NMR Kinetics. Part 89. Nuclear and Electronic Relaxation of Eu2+(aq): An Extremely Labile Aqua Ion

ChemInform, 2000-02, Vol.31 (5), p.no-no

2000

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ChemInform Abstract: High‐Pressure NMR Kinetics. Part 89. Nuclear and Electronic Relaxation of Eu 2+ (aq) : An Extremely Labile Aqua Ion

ChemInform, 2000-02, Vol.31 (5)

2000

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ChemInform Abstract: Structure and Mechanism of Hydrolysis of Diaryl(acylamino)(chloro)‐λ 4 ‐sulfanes and Diaryl(acylamino)sulfonium Salts

ChemInform, 2001-06, Vol.32 (23)

2001

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ChemInform Abstract: Structure and Mechanism of Hydrolysis of Diaryl(acylamino)(chloro)-λ4-sulfanes and Diaryl(acylamino)sulfonium Salts

ChemInform, 2001-06, Vol.32 (23), p.no-no

2001

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Multi-Membered O
(4)
S-Heterocycles
(4)
Structure
(4)
Thiazine Derivatives
(4)
Multi‐membered O,n,s‐heterocycles
(3)
Amino Acids
(2)
Amino Acids, Peptides
(2)
Antibiotics
(2)
Isoquinoline Derivatives
(2)
Peptides
(2)
Ring Closure Reactions
(2)
Alkaloids
(1)
Amino Alcohols
(1)
Analytical Chemistry
(1)
Analytical Chemistry, Review
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Anticancer Activity
(1)
Anticarcinogenic Activity
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Anticarcinogenic Activity, Anticancer Activity
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Beta
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Cadmium
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ChemInform Abstract: Peroxido Complexes of Vanadium(V) as Ligands. Crystal Structures of [Cd(NH3)6] [{VO(O2)2(OH)}2{μ-Cd (NH3)4}] and [{VO(O2)2(Im)}2{μ-Cu(Im)4}] (Im = Imidazole)

HPLC Separation of Amino Acid Enantiomers and Small Peptides on Macrocyclic Antibiotic Based Chiral Stationary Phases

One-Pot Synthesis of N-Protected β-Chiral Amino Alcohols

4-Amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic Acid (β-TOAC), the First Spin-Labeled, Cyclic, Chiral β-Amino Acid Resolved in an Enantiomerically Pure State

ChemInform Abstract: Convenient Synthesis of 3,4-Methano-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acid (VIII) and Its Derivatives (VII) as Doubly Constrained Nonproteinogenic Amino Acid Derivatives

ChemInform Abstract: Ring Transformations of β-Lactam-Condensed 1,3-Benzothiazines to Isoquinoline and Thiazole Derivatives by Sulfur Extrusion and Addition Sequences

ChemInform Abstract: Ring Transformations of [beta]-Lactam-Condensed 1,3-Benzothiazines to Isoquinoline and Thiazole Derivatives by Sulfur Extrusion and Addition Sequences

ChemInform Abstract: One-Step Ring-Closure Procedure for 4,5-Dihydro-1,3-thiazino[5,4-b]indole Derivatives with Lawesson′s Reagent. The Fifth Dihydro-1,3-thiazino[b]indole Isomer

ChemInform Abstract: One-Step Ring-Closure Procedure for 4,5-Dihydro-1,3-thiazino[5,4-b]indole Derivatives with Lawesson's Reagent. The Fifth Dihydro-1,3-thiazino[b]indole Isomer

ChemInform Abstract: A Convenient Synthesis of 1,4-Benzothiazepines from 1,3-Benzothiazines via the Ring Transformation of β-Lactam-Condensed 1,3-Benzothiazine Derivatives

ChemInform Abstract: Unexpected Formation of Indenoisoquinoline Derivatives from Thia Analogues of Protoberberine Alkaloids

ChemInform Abstract: Staudinger and retro-Staudinger Reactions. The Dichloro-β-lactam Moiety as a Useful Handle for the Synthesis of 4-Aryl-2H-1,3-benzothiazine 1,2-Dioxides

ChemInform Abstract: Expected and Unexpected Reactions of 1,3-Benzothiazine Derivatives. Part 2. Formation of Isomeric 5,6-Dihydro-1,5-benzothiazocines

ChemInform Abstract: Expected and Unexpected Reactions of 1,3-Benzothiazine Derivatives. Part 1. Ring Transformation of β-Lactam-Condensed 1,3-Benzothiazines into 4,5-Dihydro-1,4-benzothiazepines and Indolo-1,4-benzothiazepines

Biosynthetic Capacities of Actinomycetes. Part 36. Fogacin (I), a Novel Cyclic Octaketide Produced by Streptomyces Strain T 6319

Biosynthetic Capacities of Actinomycetes. Part 32. Retymicin (I), Galtamycin B (II), Saquayamycin Z and Ribofuranosyllumichrome (III), Novel Secondary Metabolites from Micromonospora sp. Tue 6368. Part 1. Taxonomy, Fermentation, Isolation and Biological Activities

Retymicin, Galtamycin B, Saquayamycin Z and Ribofuranosyllumichrome, Novel Secondary Metabolites from Micromonospora sp. Tue 6368. Part 2. Structure Elucidation

ChemInform Abstract: High-Pressure NMR Kinetics. Part 89. Nuclear and Electronic Relaxation of Eu2+(aq): An Extremely Labile Aqua Ion

ChemInform Abstract: High‐Pressure NMR Kinetics. Part 89. Nuclear and Electronic Relaxation of Eu 2+ (aq) : An Extremely Labile Aqua Ion

ChemInform Abstract: Structure and Mechanism of Hydrolysis of Diaryl(acylamino)(chloro)‐λ 4 ‐sulfanes and Diaryl(acylamino)sulfonium Salts

ChemInform Abstract: Structure and Mechanism of Hydrolysis of Diaryl(acylamino)(chloro)-λ4-sulfanes and Diaryl(acylamino)sulfonium Salts

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