Results 11 to 20 of about 14,649 (249)

Enantioselective synthesis of (−)-paeonilide [PDF]

open access: yesChemical Communications, 2012
The first enantioselective synthesis of (−)-paeonilide is reported. Starting from inexpensive furan-3-carboxylic acid the targeted monoterpene was obtained in 12 steps via an asymmetric cyclopropanation-lactonization cascade and a stereoselective side chain insertion at an acetal-like position.
Harrar, Klaus, Reiser, Oliver
openaire   +3 more sources

Enantioselective Synthesis of (−)-Acetylapoaranotin

open access: yesOrganic Letters, 2017
The first enantioselective total synthesis of the epipolythiodiketopiperazine (ETP) natural product (-)-acetylapoaranotin (3) is reported. The concise synthesis was enabled by an eight-step synthesis of a key cyclohexadienol-containing amino ester building block.
Haoxuan Wang   +5 more
openaire   +4 more sources

Enantioselective Synthesis of Azamerone [PDF]

open access: yesJournal of the American Chemical Society, 2018
A concise and selective synthesis of the dichlorinated meroterpenoid azamerone is described. The paucity of tactics for the synthesis of chiral organochlorides motivated the development of unique strategies for accessing these motifs in enantioenriched forms.
Matthew L. Landry   +2 more
openaire   +3 more sources

Alilação e crotilação catalítica e enantiosseletiva de aldeídos

open access: yesQuímica Nova, 2006
The field of chiral catalysis has experienced explosive growth over the last two decades. By now, many of the classical reactions in organic synthesis can be carried out efficiently in asymmetric manner.
Fátima Ângelo de   +2 more
doaj   +3 more sources

Enantioselective Copper-Catalyzed Cyanation of Remote C(sp3)-H Bonds Enabled by 1,5-Hydrogen Atom Transfer

open access: yesiScience, 2019
Summary: The direct functionalization of C(sp3)-H bonds has led to the development of methods to access molecules or intermediates from basic chemicals in an atom- and step-economic fashion.
Cheng-Yu Wang   +5 more
doaj   +1 more source

Towards stereochemical control: A short formal enantioselective total synthesis of pumiliotoxins 251D and 237A

open access: yesBeilstein Journal of Organic Chemistry, 2013
A concise enantioselective synthesis of the advanced intermediate 5 for the synthesis of pumiliotoxins (Gallagher’s intermediate) is described. The synthesis started from the regio- and trans-diastereoselective (dr = 98:2) reductive 3-butenylation of (R)-
Jie Zhang   +2 more
doaj   +1 more source

Enantioselective Synthesis of cis-Decalins Using Organocatalysis and Sulfonyl Nazarov Reagents

open access: yesMolecules, 2015
The first organocatalytic synthesis of cis-decalins using sulfonyl Nazarov reagents is reported. The Jørgensen’s catalyst directs this highly enantioselective synthesis using different cyclohexenal derivatives.
Javier Peña   +6 more
doaj   +1 more source

Enantioselective Synthesis of (−)-Basiliskamide A [PDF]

open access: yesOrganic Letters, 2012
Basiliskamide A is an antifungal polyketide natural product isolated by Andersen and co-workers from a Bacillus laterosporus isolate, PNG-276. A nine-step enantioselective synthesis of (-)-basiliskamide A is reported, starting from commercially available β-hydroxy ester 7.
Ming, Chen, William R, Roush
openaire   +2 more sources

Chromium(II)-catalyzed enantioselective arylation of ketones

open access: yesBeilstein Journal of Organic Chemistry, 2016
The chromium-catalyzed enantioselective addition of carbo halides to carbonyl compounds is an important transformation in organic synthesis. However, the corresponding catalytic enantioselective arylation of ketones has not been reported to date. Herein,
Gang Wang   +4 more
doaj   +1 more source

Enantioenriched α-substituted glutamates/pyroglutamates via enantioselective cyclopropenimine-catalyzed Michael addition of amino ester imines

open access: yesBeilstein Journal of Organic Chemistry, 2021
A procedure for the enantioselective synthesis of α-substituted glutamates and pyroglutamates via a cyclopropenimine-catalyzed Michael addition of amino ester imines is described.
Zara M. Seibel   +2 more
doaj   +1 more source

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