نتایج جستجو برای: diels alder reaction

تعداد نتایج: 415019  

Journal: :Chemical communications 2016
B Rühle S Datz C Argyo T Bein J I Zink

A novel thermoresponsive snaptop for stimulated cargo release from superparamagnetic iron oxide core - mesoporous silica shell nanoparticles based on a [2 + 4] cycloreversion reaction (retro-Diels Alder reaction) is presented. The non-invasive external actuation through alternating magnetic fields makes this material a promising candidate for future applications in externally triggered drug del...

Journal: :Journal of the American Chemical Society 2009
Pingfan Li Hisashi Yamamoto

Lewis acid catalyzed inverse-electron-demand Diels-Alder reaction of tropone derivatives was developed. Up to 97% ee was obtained for the chiral dinucleus BINOL-aluminum complex catalyzed reaction between tropones and ketene diethyl acetal to give bicyclo[3.2.2] ring structures, which opens up a unique way of making chiral seven-membered rings.

Journal: :Chemical communications 2013
Yihui Bai Jing Yin Wei Kong Mengyi Mao Gangguo Zhu

A Pd-catalyzed addition of boronic acids to ynol ethers has been realized, delivering trisubstituted vinyl ethers in good yields with perfect control of the regio- and stereoselectivity. The reaction proceeds under mild conditions and exhibits excellent functional group compatibility. Moreover, the resultant products can be converted into pentasubstituted benzenes via the tandem Diels-Alder/aro...

Journal: :Bioscience, Biotechnology, and Biochemistry 2021

ABSTRACT An enantioselective synthesis of (3S,3aS,7aR)-wine lactone, a major aroma component white wine and citrus juices, was achieved starting from (S)-2-methyl-3-butenoic acid. intramolecular Diels–Alder reaction employed as key step.

Journal: :Acta Crystallographica Section A Foundations of Crystallography 1987

Journal: :Organics 2022

The [2+2+2] cycloaddition (homo-Diels–Alder reaction) of N-substituted 1,2,4-triazoline-3,5-diones (TADs) with bicycloalkadienes produces strained heterocyclic compounds. A reaction the unsubstituted dienes occurs readily to produce only expected homo-Diels–Alder adducts. However, previous work in literature showed that attachment a single electron-withdrawing group diene system results formati...

Journal: :Organic letters 2002
Yu Yuan Xin Li Kuiling Ding

[reaction: see text] A highly efficient aza Diels-Alder reaction of Danishefsky's diene with imines was found to occur in methanol in the absence of any acids at room temperature to give corresponding 2-substituted dihydro-4-pyridone derivatives in high yields. This reaction can be also carried out in a three-component one-pot reaction manner. The reaction was found to proceed through a Mannich...

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