Literature DB >> 11712190

Salt effects on Diels-Alder reaction kinetics.

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Year:  2001        PMID： 11712190     DOI： 10.1021/cr990410+

Source DB:  PubMed          Journal:  Chem Rev        ISSN： 0009-2665            Impact factor:   60.622


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  11 in total

1.  Amino acid side chain interactions in the presence of salts.

Authors:  Sergio A Hassan
Journal:  J Phys Chem B       Date:  2005-11-24       Impact factor: 2.991

2.  CaCl(2) as a bifunctional reusable catalyst: diversity-oriented synthesis of 4H-pyran library under ultrasonic irradiation.

Authors:  Hamid Reza Safaei; Mohsen Shekouhy; Athar Shirinfeshan; Sudabeh Rahmanpur
Journal:  Mol Divers       Date:  2012-09-12       Impact factor: 2.943

3.  A thermal dehydrogenative Diels-Alder reaction of styrenes for the concise synthesis of functionalized naphthalenes.

Authors:  Laura S Kocsis; Erica Benedetti; Kay M Brummond
Journal:  Org Lett       Date:  2012-08-22       Impact factor: 6.005

4.  Design and synthesis of (E)-1-((3-ethyl-2,4,4-trimethylcyclohex-2-enylidene)methyl-4-substituted benzenes from 1-(2,6,6-trimethylcyclohex-1-enyl)ethanol.

Authors:  Bhaskar C Das; Sakkarapalayam M Mahalingam; Todd Evans; George W Kabalka; J Anguiano; K Hema
Journal:  Chem Commun (Camb)       Date:  2009-03-09       Impact factor: 6.222

5.  Salt Effect Accelerates Site-Selective Cysteine Bioconjugation.

Authors:  Peng Dai; Chi Zhang; Matthew Welborn; James J Shepherd; Tianyu Zhu; Troy Van Voorhis; Bradley L Pentelute
Journal:  ACS Cent Sci       Date:  2016-08-25       Impact factor: 14.553

6.  Ionic liquids: just Molten salts after all?

Authors:  Hon Man Yau; Si Jia Chan; Stephen R D George; James M Hook; Anna K Croft; Jason B Harper
Journal:  Molecules       Date:  2009-07-13       Impact factor: 4.411

Review 7.  An overview of the cycloaddition chemistry of fulvenes and emerging applications.

Authors:  Ellen Swan; Kirsten Platts; Anton Blencowe
Journal:  Beilstein J Org Chem       Date:  2019-09-06       Impact factor: 2.883

8.  Diastereoselective synthesis of nitroso acetals from (S,E)-γ-aminated nitroalkenes via multicomponent [4 + 2]/[3 + 2] cycloadditions promoted by LiCl or LiClO4.

Authors:  Leandro Lara de Carvalho; Robert Alan Burrow; Vera Lúcia Patrocinio Pereira
Journal:  Beilstein J Org Chem       Date:  2013-04-30       Impact factor: 2.883

9.  Electronic Structure Analysis of the Diels-Alder Cycloaddition Catalyzed by Alkali-Exchanged Faujasites.

Authors:  Roderigh Y Rohling; Ionut C Tranca; Emiel J M Hensen; Evgeny A Pidko
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2018-06-08       Impact factor: 4.126

10.  A K+-promoted Diels-Alder reaction by using a self-assembled macrocyclic boronic ester containing two crown ether moieties.

Authors:  Kosuke Ono; Morikazu Niibe; Nobuharu Iwasawa
Journal:  Chem Sci       Date:  2019-07-03       Impact factor: 9.825
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