Results 211 to 220 of about 19,176 (260)

Inverting the Diastereoselectivity of the Mukaiyama–Michael Addition with Graphite-Based Catalysts

open access: yesACS Catalysis, 2014
Here, we show that graphite-based catalysts, mainly graphite oxide (GO) and exfoliated GO, are effective recyclable catalysts for a relevant stereoselective Mukaiyama− Michael addition, outperforming currently available catalysts.
Maria Rosaria Acocella   +2 more
exaly   +1 more source

Photoinduced Diastereoselective Aminoalkylation of Cubanes

Organic Letters, 2023
The unique properties of rigid, nonconjugated hydrocarbons provide many opportunities to design molecular building blocks for a variety of applications, but the development of suitable conditions for alkylation of cubanes is quite challenging. Herein, a photoinduced method for aminoalkylation of cubanes is reported. The benign conditions reported allow
Guillaume Levitre   +2 more
openaire   +2 more sources

Diastereoselective Total Synthesis of Raputindole A

Organic Letters, 2018
The first diastereoselective total synthesis of the bisindole alkaloid raputindole A is reported. After Au(I)-catalyzed assembly of the cyclopenta[ f]indole tricycle, it was possible to hydrogenate the indene double bond regio- and diastereoselectively through iridium catalysis, guided by a preinstalled hydroxy function.
Mario Kock, Thomas Lindel
openaire   +2 more sources

Diastereoselective Alkylations of a Protected Cysteinesulfenate

The Journal of Organic Chemistry, 2009
To further understand stereoselection in the alkylation of sulfenate anions, a protected cysteinesulfenate was generated in THF solution at low temperature. Introduction of a reactive alkylating agent brings about a cysteinyl sulfoxide in 51-75% yield, with diastereomeric ratios at the sulfinyl group ranging from 83:17 to 95:5.
Adrian L, Schwan   +4 more
openaire   +2 more sources

Diastereoselective epoxidation of dipeptide olefins

Tetrahedron Letters, 1993
Abstract m-Chloroperbenzoic acid (MCPBA) epoxidation of dipeptide olefins proceeds in high syndiastereoselectivity (38:1–300:1). This is partially caused by conformational constants introduce by the side chain that orients the allylic NH in a favorable position for hydrogen bonding to MCPBA.
S. ROMEO, D. RICH
openaire   +1 more source

Cyclohexylcarbonitriles: Diastereoselective Arylations with TMPZnCl·LiCl

The Journal of Organic Chemistry, 2012
Deprotonating substituted cyclohexanecarbonitriles with TMPZnCl·LiCl affords zincated nitriles that diastereoselectively couple with aryl bromides in the presence of catalytic Pd(OAc)(2) and S-Phos. Steric and electronic effects influence the diastereoselectivity; 4-t-butyl-, 4-TBSO-, and 2-Me-cyclohexanecarbonitriles exert virtually complete ...
Robert J, Mycka   +5 more
openaire   +2 more sources

Diastereoselective Total Synthesis of (−)-Galiellalactone

The Journal of Organic Chemistry, 2015
An enantioselective total synthesis of (-)-galiellalactone has been accomplished. The key features of the synthesis involve the highly stereoselective construction of the cis-trisubstituted cyclopentane intermediate by a Pd(0)-catalyzed cyclization, the stereospecific introduction of an angular hydroxyl group by Riley oxidation, and the efficient ...
Taewoo, Kim   +5 more
openaire   +2 more sources

Diastereoselective Preparation of Azetidines and Pyrrolidines

Organic Letters, 2010
Iodine-mediated cyclization of homoallyl amines at room temperature delivered cis-2,4-azetidine through a 4-exo trig cyclization. Isomerization of iodo-azetidines to cis-pyrrolidines could be achieved by heating, with complete stereocontrol. The relative stereochemistry of the iodo-azetidines and pyrrolidines was confirmed by NMR spectroscopy and X-ray
Antonio, Feula   +2 more
openaire   +2 more sources

Diastereoselective Hydroboration of Isopropenylcyclopropanes

The Journal of Organic Chemistry, 1999
Janine, Cossy   +3 more
openaire   +2 more sources

Diastereoselection through chiral conformations.

Enantiomer, 2000
Chiral conformations of flexible molecules may develop in a concerted manner if the molecule is crowded enough to assure sufficient level of through-the-space contacts. Higher number (> 4) of groups connected to the same atom, as in many coordination compounds, can be advantageous in this respect.
M. Szabo   +6 more
openaire   +3 more sources

Home - About - Disclaimer - Privacy