Results 131 to 140 of about 3,980 (188)

A convenient synthesis of macrocyclic lactams

Tetrahedron Letters, 1990
Abstract A facile method is described for the synthesis of macrocyclic lactams using dicarboxylic acids and diamines directly in the presence of diphenylphosphoryl azide.
Qian Ligang   +3 more
openaire   +1 more source

Radical Photocyclization Route for Macrocyclic Lactone Ring Expansion and Conversion to Macrocyclic Lactams and Ketones

The Journal of Organic Chemistry, 2013
A new method for the synthesis of macrocyclic lactones, lactams, and ketones, which utilizes photoinduced intramolecular radical cyclization reactions of substrates containing tethered carboxylic acids and α,β-unsaturated carbonyl moieties, has been uncovered.
Keisuke, Nishikawa   +7 more
openaire   +2 more sources

Access to macrocyclic lactams. Application to a new series: the dibenzotetralactams

Tetrahedron Letters, 1995
Abstract A facile route is described for the synthesis of macrocyclic dibenzotetralactams derived from 1,2-diaminobenzene based on a stepwise approach using diacid dichlorides or mixed pivalic dianhydrides for ring closure. This method is applicable for the preparation of a variety of receptors of various ring size, heteroatom substitution and ...
Nathalie Arnaud   +3 more
openaire   +2 more sources

ChemInform Abstract: A Convenient Synthesis of Macrocyclic Lactams.

ChemInform, 1992
AbstractChemInform 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.
L. QIAN   +3 more
openaire   +1 more source

Synthesis of new macrocyclic lactams, lactones, and thiolactones

Chemistry of Heterocyclic Compounds, 1996
A general method has been developed for the preparation of 14-remembered cyclic lactams, lactones, and thiolactones from heteroaromatic amino acids.
A. A. Yavolovskii   +2 more
openaire   +1 more source

Meta-Substituted Benzofused Macrocyclic Lactams as Zinc Metalloprotease Inhibitors

Journal of Medicinal Chemistry, 1997
The design, synthesis, and biochemical profile of meta-substituted benzofused macrocyclic lactams are described. The meta-substituted benzofused macrocyclic lactams were designed to have a degree of flexibility allowing the amide bond to occupy two completely different conformations while maintaining sufficient rigidity to allow for strong interaction ...
G M, Ksander   +5 more
openaire   +2 more sources

Ortho-Substituted Benzofused Macrocyclic Lactams as Zinc Metalloprotease Inhibitors

Journal of Medicinal Chemistry, 1997
The design and preparation of ortho-substituted benzofused macrocyclic lactams are described. The benzofused macrocyclic lactams were designed as neutral endopeptidase 24.11 (NEP) inhibitors. Docking studies were carried out in a model of thermolysin (TLN) using the MACROMODEL and QXP modeling programs to select suitable ring sizes.
G M, Ksander   +6 more
openaire   +2 more sources

ChemInform Abstract: A NEW SYNTHESIS OF AMIDES AND MACROCYCLIC LACTAMS

Chemischer Informationsdienst, 1979
AbstractCarbonsäuren (I) reagieren mit Brenzcatechin‐boran und ähnlichen Estern zu den aktivierten Estern (II), die mit Aminen (III) unter Eliminierung der Borinsäureester (V) glatt zu den Amiden (IV) führen.
D. B. COLLUM, S. C. CHEN, B. GANEM
openaire   +1 more source

Fluorescence quantum yield of the two novel macrocyclic lactams

Russian Journal of Physical Chemistry A, 2014
Fluorescence quantum yield of two novel compounds—dibenzo[c,k]-1,2-dithia-6,9-diazacyclododecane-5,10-dione (1) and dibenzo[c,k]-1,2-dithia-6,9-diaza-7-methylcyclododecane-5,10-dione (2) was studied by Williams method using anthracene as a reference.
Saeedeh Sepehrikia   +2 more
openaire   +1 more source

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