The oxa-Michael reaction: from recent developments to applications in natural product synthesis
CF Nising, S Bräse - Chemical Society Reviews, 2008 - pubs.rsc.org
In marked contrast to Michael reactions, oxa-Michael reactions have not been used as
standard transformations in organic synthesis until quite recently. This was mainly due to a …
standard transformations in organic synthesis until quite recently. This was mainly due to a …
Cinchona alkaloids in asymmetric organocatalysis
T Marcelli, H Hiemstra - Synthesis, 2010 - thieme-connect.com
This article reviews the applications of cinchona alkaloids as asymmetric catalysts. In the last
few years, characterized by the resurgence of interest in asymmetric organocatalysis …
few years, characterized by the resurgence of interest in asymmetric organocatalysis …
Desymmetrization of cyclohexadienones via Brønsted acid-catalyzed enantioselective oxo-Michael reaction
Q Gu, ZQ Rong, C Zheng, SL You - Journal of the American …, 2010 - ACS Publications
Desymmetrization of cyclohexadienones via enantioselective oxo-Michael reaction
catalyzed by chiral phosphoric acid to afford highly enantioenriched 1, 4-dioxane and …
catalyzed by chiral phosphoric acid to afford highly enantioenriched 1, 4-dioxane and …
A short biomimetic synthesis of the meroterpenoids guajadial and psidial A
AL Lawrence, RM Adlington, JE Baldwin, V Lee… - Organic …, 2010 - ACS Publications
The biosynthesis of the meroterpenoid guajadial was previously hypothesized to occur via a
hetero-Diels− Alder reaction between caryophyllene and an o-quinone methide. This …
hetero-Diels− Alder reaction between caryophyllene and an o-quinone methide. This …
[HTML][HTML] Biochemical evaluation of a series of synthetic chalcone and hydrazide derivatives as novel inhibitors of cruzain from Trypanosoma cruzi
DM Borchhardt, A Mascarello, LD Chiaradia… - Journal of the Brazilian …, 2010 - SciELO Brasil
Chagas' disease, a parasitic infection widely distributed throughout Latin America, is a major
public health problem with devastating consequences in terms of human morbidity and …
public health problem with devastating consequences in terms of human morbidity and …
Organocatalytic, enantioselective, intramolecular oxa-Michael reaction of alkoxyboronate: a new strategy for enantioenriched 1-substituted 1, 3-dihydroisobenzofurans
An unprecedented strategy for the synthesis of enantioenriched 1-substituted 1, 3-
dihydroisobenzofurans via an enantioselective oxa-Michael reaction of o-alkoxyboronate …
dihydroisobenzofurans via an enantioselective oxa-Michael reaction of o-alkoxyboronate …
One‐Step Multigram‐Scale Biomimetic Synthesis of Psiguadial B
A gram‐scale synthesis of psiguadial B, a purported inhibitor of human hepatoma cell
growth, has been achieved in one step by a biomimetic three‐component coupling of …
growth, has been achieved in one step by a biomimetic three‐component coupling of …
Enantioselective copper-catalyzed alkynylation of benzopyranyl oxocarbenium ions
HD Srinivas, P Maity, GPA Yap… - The Journal of organic …, 2015 - ACS Publications
We have developed highly enantioselective, copper-catalyzed alkynylations of
benzopyranyl acetals. By using a copper (I) catalyst equipped with a chiral bis (oxazoline) …
benzopyranyl acetals. By using a copper (I) catalyst equipped with a chiral bis (oxazoline) …
Asymmetric ring-opening of cyclopropyl ketones with β-naphthols catalyzed by a chiral N, N′-dioxide–scandium (iii) complex
A catalytic asymmetric ring-opening reaction of cyclopropyl ketones with β-naphthols has
been accomplished. In the presence of a chiral N, N′-dioxide/scandium (III) complex, a …
been accomplished. In the presence of a chiral N, N′-dioxide/scandium (III) complex, a …
Attrition-enhanced deracemization and absolute asymmetric synthesis of flavanones from prochiral precursors
Seven racemic 5, 7-dimethoxyflavanones afforded conglomerate crystals upon
recrystallization from a solvent. Three methodologies were investigated to achieve …
recrystallization from a solvent. Three methodologies were investigated to achieve …