Results 91 to 100 of about 27,319 (289)

Synthetic explorations of the briarane jungle: progress in developing a synthetic route to a common family of diterpenoid natural products [PDF]

open access: yesRoyal Society Open Science, 2018
The briarane diterpenoids are a large family of marine natural products that have been primarily isolated from gorgonian octocorals around the world.
Nicholas G. Moon, Andrew M. Harned
doaj   +1 more source

Unlocking a Nitrosuccinate Lyase for Decarboxylative Enzymatic Hydronitration

open access: yesAngewandte Chemie, EarlyView.
The nitrosuccinate lyase CreD catalyzes C–NO2 bond formation using nitrite in water and shows synthetic practicality with high turnover numbers up to 102,000. A combination of protein engineering and computational methods helped to reveal the mechanistic principles that underpin this unique enzymatic activity.
Matteo Aleotti   +9 more
wiley   +2 more sources

Understand the Specific Regio- and Enantioselectivity of Fluostatin Conjugation in the Post-Biosynthesis

open access: yesBiomolecules, 2020
Fluostatins, benzofluorene-containing aromatic polyketides in the atypical angucycline family, conjugate into dimeric and even trimeric compounds in the post-biosynthesis.
Yuanqi Wang   +4 more
doaj   +1 more source

Origins of Stereoselectivity in the α-Alkylation of Chiral Hydrazones

open access: yes, 2016
Density functional theory calculations and experiment reveal the origin of stereoselectivity in the deprotonation−alkylation of chiral N-amino cyclic carbamate (ACC) hydrazones. When the ACC is a rigid, camphor-derived carbamate, the two conformations of
Sarah E. Wengryniuk (1991857)   +4 more
core   +3 more sources

A stereoselective synthesis of (−)-tetrahydrolipstatin [PDF]

open access: yesChemical Communications, 1999
A stereoselective synthesis of (–)-tetrahydrolipstatin has been accomplished utilizing olefin metathesis of an acrylate ester as the key step.
Arun K, Ghosh, Chunfeng, Liu
openaire   +2 more sources

A Circular and Tacticity‐Independent Crystalline Mono‐Substituted Nylon‐6 Platform: Unexpected Large Positional Effects on Crystallizability and Performance

open access: yesAngewandte Chemie, EarlyView.
Methyl substitution positions on the nylon‐6 backbone markedly affect crystallizability, thermomechanical properties, and recyclability of the resulting atactic nylon‐6 variants. While γ‐methyl substitution gives an amorphous nylon, all other four methyl‐substitution positions (α, β, δ, and ε) afford, unexpectedly, crystalline nylons, showing tacticity‐
Jun‐Jie Tian   +9 more
wiley   +2 more sources

Synthetic avenues towards a tetrasaccharide related to Streptococcus pneumonia of serotype 6A

open access: yesBeilstein Journal of Organic Chemistry, 2018
Streptococcus pneumonia (SPn) is a Gram-positive bacterium which causes life threatening diseases. The bacteria protect themselves against non-specific host defence by an external polysaccharide (PS) capsule which bears a repeating unit, α-D-Galp(1->3)-α-
Aritra Chaudhury   +2 more
doaj   +1 more source

How O-Substitution of Sialyl Donors Affects Their Stereoselectivity

open access: yes, 2016
The profound effect of substituents at C-5 of glycosyl sialosides on their stereoselectivity is well-known although the exact nature of this effect is somewhat less understood.
Cristina De Meo (1535950)   +5 more
core   +2 more sources

Stereoselective synthesis of tetrasubstituted alkenes via a sequential carbocupration and a new sulfur–lithium exchange

open access: yesBeilstein Journal of Organic Chemistry, 2012
We have designed a new sequential carbocupration and sulfur–lithium exchange that leads stereo- and regioselectively to trisubstituted alkenyllithiums.
Andreas Unsinn, Cora Dunst, Paul Knochel
doaj   +1 more source

N-Heterocyclic carbene/Brønsted acid cooperative catalysis as a powerful tool in organic synthesis

open access: yesBeilstein Journal of Organic Chemistry, 2012
The interplay between metals and N-heterocyclic carbenes (NHCs) has provided a window of opportunities for the development of novel catalytic strategies within the past few years.
Rob De Vreese, Matthias D’hooghe
doaj   +1 more source

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