Results 141 to 150 of about 754 (188)
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Spiroannulation by Alkylation and Reductive Cyclization of Nitriles

Angewandte Chemie International Edition, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Scott D, Rychnovsky, Leo R, Takaoka
openaire   +2 more sources

A chemo- and regioselective Pd(0)-catalyzed three-component spiroannulation

Chemical Communications, 2021
A novel Pd(0)-catalyzed three-component [2+2+1] dearomatizing reaction for the highly chemo- and regio-selective assembly of spirocarbocycles is described.
Jiaoyu Wu   +4 more
openaire   +2 more sources

ChemInform Abstract: Cyclic Ketones in Spiroannulation.

ChemInform, 2009
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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.
Vidar Bjoernstad, Kjell Undheim
openaire   +1 more source

Synthesis of spiroannulated oligopyrrole macrocycles derived from lithocholic acid

Steroids, 2009
Two new steroidal spiroannulated calix[4]pyrroles 5 and 10, derived from bile acids (lithocholate), were prepared by the acid catalyzed condensation of methyl-3,3-bis(pyrrol-2-yl)-5beta-cholan-24-oate 3 with carbonyl compounds and with 2,2'-propane-2,2-diylbis(1H-pyrrole), respectively.
Thi Thu Huong N   +4 more
openaire   +4 more sources

Rh(III)-Catalyzed C8-Spiroannulation of 1-Aminonaphthalenes with Maleimides

The Journal of Organic Chemistry, 2023
The rhodium(III)-catalyzed C8-spiroannulation of 1-aminonaphthalenes with maleimides is described herein. Initially formed C8-alkenylated 1-aminonaphthalenes can intercept nucleophilic 1-amino groups through the intramolecular aza-Michael reaction, resulting in the formation of spirofused tetracyclic frameworks. This protocol displayed a wide substrate
Eunjae Chung   +6 more
openaire   +2 more sources

.alpha.-Substitution-spiroannulation of saturated ketones

Journal of the American Chemical Society, 1983
α-Substitution-spiroannelation de la cyclopentanone.
Barry M. Trost, Michael K. T. Mao
openaire   +1 more source

Spiroannulation approach to pentalenene, an angular triquinane sesquiterpene

The Journal of Organic Chemistry, 1994
The route to the angular triquinane (±)-pentalenene (1a) followed from an efficient geminal acylation of the acetal of isophorone or its homolog 6b by 1,2-bis((trimethylsilyl)oxy)cyclobutene (3) in the presence of boron trifluoride etherate. Ring cleavage and reclosure (9→11) secured the required spiro[4.4] nonane system with a pendant ketone function ...
Y.-J. Wu, Y.-Y. Zhu, D. Jean Burnell
openaire   +1 more source

Enantioselective Synthesis of Ring-Fused Spiroannulated 1,2,3-Thiadiazole Derivatives

The Journal of Organic Chemistry, 2016
An organocatalytic enantioselective domino α-amination/oxidative coupling/cyclization of thioamides to azodicarboxylates catalyzed by an easily available organic catalyst has been developed. The key step, oxidative coupling, is smoothly fulfilled in air.
Xue-Mei, Zeng, Jian-Wu, Xie
openaire   +2 more sources

Gold(I)-Catalyzed Ring-Expanding Spiroannulation of Cyclopropenones with Enynes

The Journal of Organic Chemistry, 2014
The gold(I)-catalyzed ring-expanding spiroannulation of cyclopropenones with enynes is reported here. A molecule of water is incorporated into the products during the spiroannulation to afford spirocyclic cyclopentenones containing an alcohol functionality.
Takanori, Matsuda, Yusuke, Sakurai
openaire   +2 more sources

ChemInform Abstract: An Efficient Asymmetric Spiroannulation Process.

ChemInform, 1990
AbstractThe keto ester (I) reacts with the chiral amine (R)‐(II) to give a mixture of diastereomers (III) which undergoes asymmetric spiroannulation, forming stereoselectively the imine (IV).
J. D'ANGELO   +3 more
openaire   +1 more source

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