Results 31 to 40 of about 2,007 (155)

Reversal of Regioselectivity in Reactions of Donor-Acceptor Cyclopropanes with Eelectrophilic Olefins

open access: yes, 2021
Cyclopropanes bearing donor and acceptor groups at the opposite ends of the C-C bond should react with both nucleophiles and electrophiles. Their reactivity towards nucleophiles is well explored while only few specific electrophilic reagents give desired
Jakub, Durka   +3 more
core   +1 more source

Bifunctional Photocatalysts: Exploiting Proximity for Enhanced Reaction Performance. [PDF]

open access: yesChemistry
This review covers the application of the bifunctional approach to photocatalysis as a means to attain (enhanced) enantioselectivity, and, more in general, as a strategy to enhance the catalytic performance through an effective use of short‐lived reaction intermediates.
Dolcini L   +3 more
europepmc   +2 more sources

Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates

open access: yesMolecules, 2018
A simple method has been developed for the synthesis of cyclopropa[c]coumarins, which belong to the donor-acceptor cyclopropane family and, therefore, are promising substrates for the preparation of chromene-based fine chemicals. The method, based on the
Olga A. Ivanova   +5 more
doaj   +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

Allylation of Donor−Acceptor Cyclopropanes

open access: yes, 2016
Direct allylation of glycal-derived donor−acceptor cyclopropanes has been achieved with TiCl4 activation followed by addition of allyltrimethylsilane. The α diastereomer is the major product, with selectivities ranging from 3:1 to 10:1 and yields around ...
Ming Yu (78996)   +1 more
core   +2 more sources

Cyclopropanes and Hypervalent Iodine Reagents: High Energy Compounds for Applications in Synthesis and Catalysis

open access: yesCHIMIA, 2011
One of the major challenges faced by organic chemistry is the efficient synthesis of increasingly complex molecules. Since October 2007, the Laboratory of Catalysis and Organic Synthesis (LCSO) at EPFL has been working on the development of ...
Davinia Fernández González   +4 more
doaj   +1 more source

Methods for the synthesis of donor-acceptor cyclopropanes

open access: yes, 2018
The interest in cyclopropane derivatives is caused by the facts that, first, the three-carbon ring is present in quite a few natural and biologically active ...
Leonid G. Menchikov   +4 more
core   +3 more sources

Cyclization of Cyclopropyl Carbonyls and the Homo-Nazarov Reaction

open access: yesCHIMIA, 2009
Ring strain confers exceptional reactivity to the cyclopropane ring. Nevertheless, activation of the cyclopropane ring is usually needed to allow ring-opening reactions under mild conditions.
Filippo De Simone, Jérôme Waser
doaj   +1 more source

4b,5,6,9-Tetrahydro-7H-dibenzo[c,e]pyrrolo[1,2-a]azepin-7-one

open access: yesMolbank, 2019
A simple approach to synthesize 4b,5,6,9-tetrahydro-7H-dibenzo[c,e]pyrrolo[1,2-a]azepin- 7-one has been developed, based on a three-step transformation of 2-(2-bromophenyl)cyclopropane-1,1-diester.
Maksim A. Boichenko   +5 more
doaj   +1 more source

Asymmetric (5 + 3) Annulation of Donor–Acceptor Cyclopropanes with Imidazolidines: Access to Saturated 1,4-Diazocanes

open access: yes, 2023
Saturated 1,4-diazocanes are highly important for medicinal chemistry and drug discovery, but their syntheses are often tedious. Herein, we report a copper-catalyzed (5 + 3) annulation of donor–acceptor cyclopropanes with imidazolidines, thereby ...
Shiyong Peng (1508452)   +7 more
core   +3 more sources

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