Results 1 to 10 of about 197,715 (144)

Enzymatic one-step ring contraction for quinolone biosynthesis [PDF]

open access: yesNature Communications, 2018
Viridicatin is a fungal alkaloid. Here, the authors identify and characterize the cyclopenase that catalyzes the last step of its biosynthesis in Aspergillus nidulans, the conversion of cyclopenin to viridicatin, and find that the reaction proceeds via ...
Shinji Kishimoto   +7 more
doaj   +4 more sources

Nucleophile-induced ring contraction in pyrrolo[2,1-c][1,4]benzothiazines: access to pyrrolo[2,1-b][1,3]benzothiazoles [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2023
Pyrrolo[2,1-b][1,3]benzothiazoles are an important class of fused sulfur and nitrogen-containing heterocycles intensively studied in medicinal chemistry and pharmacology.
Ekaterina A. Lystsova   +3 more
doaj   +2 more sources

Pyrrolidine synthesis via ring contraction of pyridines [PDF]

open access: yesNature Communications
A ring contraction of easily available cyclic compounds to smaller cycles that are valuable but difficult to synthetically access is one of important skeletal editing strategies.
Ryoga Ueno, Shohei Hirano, Jun Takaya
doaj   +2 more sources

Curvature-induced expulsion of actomyosin bundles during cytokinetic ring contraction [PDF]

open access: yeseLife, 2016
Many eukaryotes assemble a ring-shaped actomyosin network that contracts to drive cytokinesis. Unlike actomyosin in sarcomeres, which cycles through contraction and relaxation, the cytokinetic ring disassembles during contraction through an unknown ...
Junqi Huang   +9 more
doaj   +2 more sources

Ring contraction and ring expansion reactions in terpenoid biosynthesis and their application to total synthesis [PDF]

open access: yesBeilstein Journal of Organic Chemistry
Terpenoids exhibit remarkable structural diversity, including highly complex ring-expanded or contracted carbocyclic skeletons. This review aims to explore intriguing examples of such ring-size alterations in all aspects of terpenoid synthesis.
Nicolas Kratena   +2 more
doaj   +2 more sources

Myo2p is the major motor involved in actomyosin ring contraction in fission yeast. [PDF]

open access: yesCurr Biol, 2017
Cytokinesis in many eukaryotes requires an actomyosin-based contractile ring [1]. In fission yeast, cytokinesis involves the type II myosins Myo2p and Myp2p and the type V myosin Myo51p [2]. A recent study by Laplante et al.
Zambon P   +3 more
europepmc   +4 more sources

Hypervalent Iodine–Mediated Ring Contraction Reactions [PDF]

open access: yesMolecules, 2006
Hypervalent iodine reagents constitute a powerful tool in modern synthetic organic chemistry, promoting several important reactions. One such reaction is the ring contraction of cycloalkenes and cycloalkanones promoted by iodine(III) compounds, such as ...
Luiz F. Silva
doaj   +4 more sources

Chiral hypervalent iodine catalyzed stereoselective skeletal editing of pyrimidine fused heterocycles [PDF]

open access: yesNature Communications
In the realm of molecular construction, the skeletal editing techniques of heterocyclic compounds demonstrate unique efficiency, particularly in synthesizing molecular structures that are challenging to obtain through traditional synthetic methods ...
Wen-Wu Sun, Yi-Bing Xie, Bin Wu
doaj   +2 more sources

Transformation of the cyclohexane ring to the cyclopentane fragment of biologically active compounds [PDF]

open access: yesBeilstein Journal of Organic Chemistry
The review is devoted to strategies for contraction of six-membered cycles in the synthesis of functionalized cyclopentane/enones, which are biologically active compounds.
Natalya Akhmetdinova   +2 more
doaj   +2 more sources

Reconstructing the magmatic crystallization conditions and alteration processes of quartz dolerites of the Kremennaya mountain stock (Mountain Crimea)

open access: yesИзвестия высших учебных заведений: Геология и разведка, 2022
Introduction. The 60 m wide quartz dolerite stock, opened by a quarry, is heavily alternated by secondary processes, which makes it difficult to study.Aim.
V. A. Utenkov, A. V. Turov
doaj   +1 more source

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