Results 51 to 60 of about 19,882 (280)

Total synthesis of avenaol

open access: yesNature Communications, 2017
Avenaol is a potent germination stimulant that can be extracted from black oat. Here, the authors report the total synthesis of avenaol by developing a strategy to access all-cis-substituted cyclopropanes.
Motohiro Yasui   +3 more
doaj   +1 more source

Orientation effects in reactions of allenyl cations with styrene [PDF]

open access: yes, 1979
Allenyl cations, generated from allenyl or alkynyl halides and Ag+, attack styrene at the side chain or at the aromatic nucleus. The allenyl/alkynyl product ratio is dependent on the structure of the precursor halide except for highly substituted ...
Bertrand   +13 more
core   +1 more source

Enantiopure Chiral Crystals: A Powerful Tool for Absolute Asymmetric Synthesis

open access: yesAsian Journal of Organic Chemistry, EarlyView.
This review covers absolute asymmetric syntheses, which allow the preparation of enantiomerically enriched chiral compounds from achiral precursors. By exploiting the crystallization of certain compounds as a conglomerate, enantiopure chiral crystals are spontaneously obtained.
Jiacheng Li, Valérie Alezra
wiley   +1 more source

Diastereo- and enantioselective [3 + 3] cycloaddition of spirocyclopropyl oxindoles using both aldonitrones and ketonitrones

open access: yesNature Communications, 2017
Chiral spirocyclic compounds are important structural motifs for drug discovery. Here, the authors report a synthetic route to spirocycles based on enantioselective cycloaddition of activated spirocyclopropyl oxindoles, which act as donor-acceptor ...
Peng-Wei Xu   +6 more
doaj   +1 more source

Types and properties of metal-free catalysts for living polymerizations of biomaterials [PDF]

open access: yes, 2008
Syntéza biokompatibilních a biodegradabilních polyesterů, použitelných převážně v medicíně, využívá pro polymeraci za otevření kruhu katalyzátory na bázi kovu (např. Sn, Al atd.), které se mohou po implantaci deponovat v těle.
Repka, Martin
core  

Organocatalytically Generated Donor − Acceptor Cyclopropanes in Domino Reactions. One-Step Enantioselective Synthesis of Pyrrolo[1,2 ‑ a ]quinolines [PDF]

open access: yes, 2016
An easy and straightforward procedure has been developed for the synthesis of highly enantioenriched pyrrolo-[1,2-a]quinolines through a one-pot process that comprises a domino cyclopropane ring opening/aza-Michael/aldol reaction followed by acid ...
Carrillo Fernández, María Luisa   +5 more
core   +2 more sources

Biosynthese des Rotalgen‐Diterpens Peyssonnosol in Bakterien

open access: yesAngewandte Chemie, EarlyView.
Zwei Terpensynthasen aus Anaerolineae‐Bakterien katalysieren die Biosynthese von Peyssonnosen‐artigen Diterpenen aus Rotalgen. Ortsgerichtete Mutagenese ermöglichte einen partiellen Funktionswechsel, der zur Bildung zusätzlicher Nebenprodukte führte.
Zhiyong Yin   +10 more
wiley   +1 more source

The Oxidative Reaction of Potassium Permanganate with Mycolic Acids Leads to a Unique Diagnostic Pattern for Mycobacterium Tuberculosis [PDF]

open access: yes, 2008
In an oxidative reaction, potassium permanganate reacts with the mycolic acid component of _M.tuberculosis_ and gives rise to a unique saponified pattern specific for _M.tuberculosis_.
Mohsen khatami
core   +1 more source

An Approach to 1,1-Disubstituted Pyrazolylcyclopropane Building Blocks

open access: yesSynOpen, 2017
An approach to isomeric 1,1-disubstituted pyrazolylcyclopropanes that relies on lithium diisopropylamide (LDA) mediated bis-alkylation­ of the corresponding pyrazolylacetonitriles is developed.
Pavel S. Nosik   +3 more
doaj   +1 more source

Synthesis of Cyclopropanes via Organoiron Methodology: Preparation of \u3cem\u3erac\u3c/em\u3e-Dysibetaine Cpa [PDF]

open access: yes, 2007
The cyclopropane containing betaine, rac-dysibetaine CPa, was prepared from (1-methoxycarbonylpentadienyl)-Fe(CO)2PPh3+ by nucleophilic addition of nitromethane anion followed by oxidatively induced reductive ...
Donaldson, William A.   +3 more
core   +1 more source

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