نتایج جستجو برای: alder

تعداد نتایج: 3751  

2001
N. S. Rojas D. A. Perry C. Y. Li L. M. Ganio

The study examined the effect of Frankia, macronutrients, micronutrients, mycorrhizal fungi, and plant-growth-promoting fluorescent Pseudomonas sp. on total biomass, nodule weight, and nitrogen fixation of red alder (Alnus rubra) and snowbrush (Ceanothus velutinus) under greenhouse conditions. The soil samples were collected from a 10-year-old clearcut on the H.J. Andrews Experimental Forest, O...

Journal: :علوم و تکنولوژی پلیمر 0
جواد ترکمن

0

Journal: :Organic & biomolecular chemistry 2013
Rui Guo Kang-Nan Li Liu-Zhu Gong

Enyne alcohols can react as precursors of either dienes or dienophiles with different substrates after hydroxylation and isomerization by gold catalysis. As such, oxa-bridged tricyclo[5.2.2.02,6]-undec-8-ene-3,5-dione derivatives have been obtained by the Diels–Alder reaction and tetrahydro-1H-furo[3,4-c]pyran derivatives could be accessed by the hetero-Diels–Alder cycloaddition.

Journal: :The Journal of organic chemistry 2007
Aitor Landa Bo Richter Rasmus Lyng Johansen Anna Minkkilä Karl Anker Jørgensen

A general catalytic oxo-hetero-Diels-Alder reaction for pro-chiral aldehyde and ketone N-oxy-pyridines is presented. The catalytic and asymmetric oxo-hetero-Diels-Alder reaction of electron-rich dienes with N-oxy-pyridine-2-carbaldehyde and ketone derivatives, catalyzed by chiral copper(II)-bisoxazoline complexes, gives optically active six-membered oxygen heterocycles in moderate to good yield...

Journal: :Organic & biomolecular chemistry 2014
Kathryn A Punch Matthew J Piggott

The first total synthesis of monosporascone is presented. The five-step synthesis developed includes a silver acetylide-acid chloride coupling, domino Diels-Alder-retro-Diels-Alder reaction, and an intramolecular Friedel-Crafts acylation, and provides the natural product in 57% yield overall. Selective reduction of monosporascone also afforded the related metabolite dihydromonosporascone.

Journal: :Dalton transactions 2016
Alan A Wiles Xiaolu Zhang Brian Fitzpatrick De-Liang Long Stuart A Macgregor Graeme Cooke

Chemical redox reactions have been exploited to transform unreactive vinylferrocene into a powerful dienophile for the Diels-Alder reaction and reactive substrate for thiol addition reactions upon conversion to its ferrocenium state. We have further investigated the ability of these reactions to facilitate redox-auxiliary-like reactivity by further hydrogenolyisis of the Diels-Alder adduct to t...

Journal: :Organic letters 2002
Eric J Tisdale Chinmay Chowdhury Binh G Vong Hongmei Li Emmanuel A Theodorakis

[reaction: see text] Two different routes to the tricyclic core of Garcinia-derived natural products are described. The first approach is based on a tandem Claisen/Diels-Alder rearrangement and delivers the desired lactone 14. The second approach, employing a Wessely oxidation/Diels-Alder protocol, leads to the same caged heterocycle, albeit with modified constitution.

Journal: :Chemical communications 2015
Zhe Ji Ji Chen Liang Huang Gaoquan Shi

On the basis of the Diels-Alder reaction of graphite and tetracyanoethylene, graphite has been mechanically exfoliated into graphene adducts in a yield up to 38%. The graphene adduct can restore its conjugated structure via retro-Diels-Alder reaction under mild conditions, exhibiting a high conductivity of 1035 S m(-1).

2018
Joseph E. Knelman Emily B. Graham Janet S. Prevéy Michael S. Robeson Patrick Kelly Eran Hood Steve K. Schmidt

Past research demonstrating the importance plant-microbe interactions as drivers of ecosystem succession has focused on how plants condition soil microbial communities, impacting subsequent plant performance and plant community assembly. These studies, however, largely treat microbial communities as a black box. In this study, we sought to examine how emblematic shifts from early successional A...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2018
Zhongyue Yang Song Yang Peiyuan Yu Yanwei Li Charles Doubleday Jiyong Park Ashay Patel Byung-Sun Jeon William K Russell Hung-Wen Liu David H Russell Kendall N Houk

SpnF is the first monofunctional Diels-Alder/[6+4]-ase that catalyzes a reaction leading to both Diels-Alder and [6+4] adducts through a single transition state. The environment-perturbed transition-state sampling method has been developed to calculate free energies, kinetic isotope effects, and quasi-classical reaction trajectories of enzyme-catalyzed reactions and the uncatalyzed reaction in ...

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