Results 221 to 230 of about 23,776 (268)
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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

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

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
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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
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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

Enantio- and diastereoselective Darzens condensations

Tetrahedron Letters, 2007
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, please click on HTML or PDF.
Achard TJR   +5 more
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Diastereoselective Synthesis of 2,3,4,5,6-Pentafluoroheptanes

The Journal of Organic Chemistry, 2009
A stereocontrolled synthesis of alkanes containing five contiguous fluorine atoms is presented. The compounds were prepared by sequential fluorination of diastereoisomeric alcohol-diepoxides. The chemistry involved epoxide ring-opening with HF.NEt(3) and deshydroxyfluorination reactions of free alcohols with Deoxo-Fluor. The fluorination reactions were
Farran, Daniel   +3 more
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A practical diastereoselective synthesis of (−)‐bestatin

Journal of Peptide Science, 2018
Diastereoselective addition of nitromethane to Boc‐D‐Phe‐H in the presence of sodium hydride in diethyl ether/hexane containing 15‐crown‐5 and subsequent N,O‐protection with 2,2‐dimethoxypropane gave trans‐oxazolidine in a diastereomeric ratio of >16:1.
Suisheng Shang   +2 more
openaire   +2 more sources

Diastereoselective Hydroboration of Isopropenylcyclopropanes

The Journal of Organic Chemistry, 1999
Janine, Cossy   +3 more
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Diastereoselective Cyclopentane Construction

The Journal of Organic Chemistry, 2000
, Taber, , Wang, , Pahutski
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