Meldrum's zuur (Dutch Wikipedia)

Analysis of information sources in references of the Wikipedia article "Meldrum's zuur" in Dutch language version.

refsWebsite

Global rank Dutch rank

14doi.org

2^nd place

8^th place

6nih.gov

4^th place

12^th place

3archive.org

6^th place

25^th place

1books.google.com

3^rd place

43^rd place

archive.org

McNab, Hamish (1978). Meldrum's acid. Chemical Society Reviews 7 (3): 345–358. DOI: 10.1039/CS9780700345.
Gaber, Abd El-Aal M., McNab, Hamish (2001). Synthetic Applications of the Pyrolysis of Meldrum's Acid Derivatives. Synthesis 2001 (14): 2059–2074. DOI: 10.1055/s-2001-18057.
Bonifácio, Vasco D. B. (2004). Meldrum's Acid. Synlett 2004 (9): 1649–1650. DOI: 10.1055/s-2004-829539.

books.google.com

Norman Meldrum, Andrew (1908). A β-lactonic acid from acetone and malonic acid. Journal of the Chemical Society, Transactions 93: 598–601. DOI: 10.1039/CT9089300598.

doi.org

McNab, Hamish (1978). Meldrum's acid. Chemical Society Reviews 7 (3): 345–358. DOI: 10.1039/CS9780700345.
Norman Meldrum, Andrew (1908). A β-lactonic acid from acetone and malonic acid. Journal of the Chemical Society, Transactions 93: 598–601. DOI: 10.1039/CT9089300598.
Nakamura, Satoshi, Hirao, Hajime, Ohwada, Tomohiko (2004). Rationale for the Acidity of Meldrum's Acid. Consistent Relation of C−H Acidities to the Properties of Localized Reactive Orbital. J. Org. Chem. 69 (13): 4309–4316. PMID 15202884. DOI: 10.1021/jo049456f.
Oikawa, Yuji, Sugano, Kiyoshi, Yonemitsu, Osamu (1978). Meldrum's acid in organic synthesis. 2. A general and versatile synthesis of β-keto esters. J. Org. Chem. 43 (10): 2087–2088. DOI: 10.1021/jo00404a066.
Ghosh, Santanu, Purkait, Anisha, Jana, Chandan K. (2020). Environmentally benign decarboxylative N -, O -, and S -acetylations and acylations. Green Chemistry 22 (24): 8721–8727. DOI: 10.1039/D0GC03731A.
Li, Jiang-Sheng, Da, Yu-Dong, Chen, Guo-Qin, Yang, Qian, Li, Zhi-Wei (13 February 2017). Solvent-, and Catalyst-free Acylation of Anilines with Meldrum's Acids: A Neat Access to Anilides. ChemistrySelect 2 (5): 1770–1773. DOI: 10.1002/slct.201601965.
Davis, Garrett J., Sofka, Holly A., Jewett, John C. (3 april 2020). Highly Stable Meldrum's Acid Derivatives for Irreversible Aqueous Covalent Modification of Amines. Organic Letters 22 (7): 2626–2629. PMID 32191483. PMC 7679203. DOI: 10.1021/acs.orglett.0c00597.
Heard, David M., Lennox, Alastair J. J. (7 May 2021). Dichloromeldrum's Acid (DiCMA): A Practical and Green Amine Dichloroacetylation Reagent. Organic Letters 23 (9): 3368–3372. PMID 33844547. DOI: 10.1021/acs.orglett.1c00850.
Gaber, Abd El-Aal M., McNab, Hamish (2001). Synthetic Applications of the Pyrolysis of Meldrum's Acid Derivatives. Synthesis 2001 (14): 2059–2074. DOI: 10.1055/s-2001-18057.
Dumas, Aaron M., Fillion, Eric (2009). Meldrum's Acids and 5-Alkylidene Meldrum's Acids in Catalytic Carbon–Carbon Bond-Forming Processes. Acc. Chem. Res. 43 (3): 440–454. PMID 20000793. DOI: 10.1021/ar900229z.
Oikawa, Yuji, Hirasawa, Hitoshi, Yonemitsu, Osamu (1978). Meldrum's acid in organic synthesis. 1. A convenient one-pot synthesis of ethyl indolepropionates. Tetrahedron Letters 19 (20): 1759–1762. DOI: 10.1016/0040-4039(78)80037-9.
Lipson, Victoria V., Gorobets, Nikolay Yu. (2009). One hundred years of Meldrum's acid: Advances in the synthesis of pyridine and pyrimidine derivatives. Mol. Divers. 13 (4): 399–419. PMID 19381852. DOI: 10.1007/s11030-009-9136-x.
Bonifácio, Vasco D. B. (2004). Meldrum's Acid. Synlett 2004 (9): 1649–1650. DOI: 10.1055/s-2004-829539.
Davidson, David, Bernhard, Sidney A. (1948). The Structure of Meldrum's Supposed β-Lactonic Acid. Journal of the American Chemical Society 70 (10): 3426–3428. PMID 18891879. DOI: 10.1021/ja01190a060.

nih.gov

ncbi.nlm.nih.gov

Nakamura, Satoshi, Hirao, Hajime, Ohwada, Tomohiko (2004). Rationale for the Acidity of Meldrum's Acid. Consistent Relation of C−H Acidities to the Properties of Localized Reactive Orbital. J. Org. Chem. 69 (13): 4309–4316. PMID 15202884. DOI: 10.1021/jo049456f.
Davis, Garrett J., Sofka, Holly A., Jewett, John C. (3 april 2020). Highly Stable Meldrum's Acid Derivatives for Irreversible Aqueous Covalent Modification of Amines. Organic Letters 22 (7): 2626–2629. PMID 32191483. PMC 7679203. DOI: 10.1021/acs.orglett.0c00597.
Heard, David M., Lennox, Alastair J. J. (7 May 2021). Dichloromeldrum's Acid (DiCMA): A Practical and Green Amine Dichloroacetylation Reagent. Organic Letters 23 (9): 3368–3372. PMID 33844547. DOI: 10.1021/acs.orglett.1c00850.
Dumas, Aaron M., Fillion, Eric (2009). Meldrum's Acids and 5-Alkylidene Meldrum's Acids in Catalytic Carbon–Carbon Bond-Forming Processes. Acc. Chem. Res. 43 (3): 440–454. PMID 20000793. DOI: 10.1021/ar900229z.
Lipson, Victoria V., Gorobets, Nikolay Yu. (2009). One hundred years of Meldrum's acid: Advances in the synthesis of pyridine and pyrimidine derivatives. Mol. Divers. 13 (4): 399–419. PMID 19381852. DOI: 10.1007/s11030-009-9136-x.
Davidson, David, Bernhard, Sidney A. (1948). The Structure of Meldrum's Supposed β-Lactonic Acid. Journal of the American Chemical Society 70 (10): 3426–3428. PMID 18891879. DOI: 10.1021/ja01190a060.