Reactivity and synthetic applications of multicomponent Petasis reactions
The Petasis boron–Mannich reaction, simply referred to as the Petasis reaction, is a
powerful multicomponent coupling reaction of a boronic acid, an amine, and a carbonyl …
powerful multicomponent coupling reaction of a boronic acid, an amine, and a carbonyl …
Carbonyl–olefin metathesis
H Albright, AJ Davis, JL Gomez-Lopez… - Chemical …, 2021 - ACS Publications
This Review describes the development of strategies for carbonyl–olefin metathesis
reactions relying on stepwise, stoichiometric, or catalytic approaches. A comprehensive …
reactions relying on stepwise, stoichiometric, or catalytic approaches. A comprehensive …
Methods utilizing first-row transition metals in natural product total synthesis
JE Zweig, DE Kim, TR Newhouse - Chemical Reviews, 2017 - ACS Publications
First-row transition-metal-mediated reactions constitute an important and growing area of
research due to the low cost, low toxicity, and exceptional synthetic versatility of these …
research due to the low cost, low toxicity, and exceptional synthetic versatility of these …
Iron(III)-catalysed carbonyl–olefin metathesis
JR Ludwig, PM Zimmerman, JB Gianino, CS Schindler - Nature, 2016 - nature.com
The olefin metathesis reaction of two unsaturated substrates is one of the most powerful
carbon–carbon-bond-forming reactions in organic chemistry. Specifically, the catalytic olefin …
carbon–carbon-bond-forming reactions in organic chemistry. Specifically, the catalytic olefin …
Recent developments in the stereoselective synthesis of α-aminoacids
RO Duthaler - Tetrahedron, 1994 - Elsevier
The a-amino-carboxylic-acids are one of the five major classes of natural products and they
exhibit.-important and diverse biological functions.',* Historically, the aminoacids have been …
exhibit.-important and diverse biological functions.',* Historically, the aminoacids have been …
A stereoselective synthesis of (−)-tetrodotoxin
A Hinman, J Du Bois - Journal of the American Chemical Society, 2003 - ACS Publications
An asymmetric synthesis of the fugu fish poison,(−)-tetrodotoxin, is described. The route to
this extraordinary target employs a number of unique transformations, foremost of which are …
this extraordinary target employs a number of unique transformations, foremost of which are …
New developments in the Peterson olefination reaction
LF Van Staden, D Gravestock, DJ Ager - Chemical Society Reviews, 2002 - pubs.rsc.org
Noteworthy developments of the Peterson olefination reaction are reviewed. Evidence for
both concerted and stepwise mechanisms for the Peterson olefination reaction is presented …
both concerted and stepwise mechanisms for the Peterson olefination reaction is presented …
1,n-Dicarbanionic Titanium Intermediates from Monocarbanionic Organometallics and Their Application in Organic Synthesis
OG Kulinkovich, A de Meijere - Chemical Reviews, 2000 - ACS Publications
Among the wide variety of organometallic compounds, the relatively cheap and safely
handled nontransition-metal derivatives, in particular organolithium, organomagnesium …
handled nontransition-metal derivatives, in particular organolithium, organomagnesium …
Total Synthesis of the Cephalotaxus Norditerpenoids (±)-Cephanolides A–D
M Haider, G Sennari, A Eggert… - Journal of the American …, 2021 - ACS Publications
Concise syntheses of the Cephalotaxus norditerpenoids cephanolides A–D (8–14 steps
from commercial material) using a common late-stage synthetic intermediate are described …
from commercial material) using a common late-stage synthetic intermediate are described …
Carbon-13 NMR chemical shift: a descriptor for electronic structure and reactivity of organometallic compounds
Conspectus Metal-bonded carbon atoms in metal–alkyl, metal–carbene/alkylidene, and
metal–carbyne/alkylidyne species often show significantly more deshielded isotropic …
metal–carbyne/alkylidyne species often show significantly more deshielded isotropic …