Results 21 to 30 of about 2,677,083 (277)

Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids

open access: yesNature Communications, 2023
The primary objective in synthetic organic chemistry is to develop highly efficient, selective, and versatile synthetic methodologies, which are essential for discovering new drug candidates and agrochemicals. In this study, we present a unified strategy
Fang-Fang Xu   +3 more
doaj   +1 more source

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.
Klaus, Harrar, Oliver, Reiser
openaire   +2 more sources

Challenging Atroposelective C–H Arylation

open access: yesSynOpen, 2020
Atropisomeric molecules are privileged scaffolds, not only as ligands for asymmetric synthesis, but also as biologically active products and advanced materials.
Joanna Wencel-Delord   +1 more
doaj   +1 more source

A Catalytic Highly Enantioselective Synthesis of Spirooxazolines [PDF]

open access: yes, 2021
A catalytic highly enantioselective synthesis of spirooxazolines is presented. Starting from readily available 2-naphthol-substituted benzamides and using catalytic amounts of a chiral triazole-substituted iodoarene catalyst, a variety of spirooxazolines
Ayham, Abazid, Boris, Nachtsheim
core   +2 more sources

Total synthesis of (-)-pyridovericin and synthetic studies towards aetheramide B [PDF]

open access: yes, 2015
In this thesis, two projects involving the total synthesis of natural products are presented. The first part gives an overview on neurodegenerative diseases and introduces the neuritogenic pyridopolyene natural product (–)-pyridovericin.
Schmid, Fabian Felix
core   +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

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

Total Enantioselective Synthesis of a Norbornene Derivative via Lewis Acid Catalyzed Asymmetric Diels-Alder Reaction using the Oppolzer\u27s Camphorsultam as a Chiral Auxilary [PDF]

open access: yes, 2023
In this paper, an efficient enantioselective synthesis of a norbornene derivative is described. Oppolzer\u27s chiral sultam-directed asymmetric Diels-alder [4+2] cycloaddition was conducted as a crucial tool to control the diastereoselectivity of the ...
Anissa, Yacin-Ali   +3 more
core   +2 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

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