Bouveault–Blanc reduction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Bouveault–Blanc reduction" in English language version.

refsWebsite

Global rank English rank

9doi.org

2^nd place

3bnf.fr

124^th place

544^th place

3nih.gov

4^th place

bnf.fr (Global: 124^th place; English: 544^th place)

gallica.bnf.fr

Bouveault, L.; Blanc, G. (1903). "Préparation des alcools primaires au moyen des acides correspondants" [Preparation of primary alcohols by means of the corresponding acids]. Compt. Rend. (in French). 136: 1676–1678.
Bouveault, L.; Blanc, G. (1904). "Transformation des acides monobasiques saturés dans les alcools primaires correspondants" [Transforming saturated monobasic acids into the corresponding primary alcohols]. Bull. Soc. Chim. Fr. (in French). 31: 666–672.
Bouveault, L.; Blanc, G. (1904). "Hydrogénation des éthers des acides possédant en outre les fonctions éther-oxyde ou acétal" [Hydrogenation of the ether of the acids furthermore possessing the ether-oxide or acetal functions]. Bull. Soc. Chim. Fr. (in French). 31 (3): 1210–1213.

doi.org (Global: 2^nd place; English: 2^nd place)

Wang, Zerong, ed. (2009). "109. Bouveault–Blanc Reduction". Comprehensive Organic Name Reactions and Reagents. pp. 493–496. doi:10.1002/9780470638859.conrr109. ISBN 978-0-471-70450-8.
Reid, E. E.; Cockerille, F. O.; Meyer, J. D.; Cox, W. M.; Ruhoff, J. R. (1935). "Oleyl Alcohol". Organic Syntheses. 15: 51. doi:10.15227/orgsyn.015.0051.
Adkins, Homer; Gillespie, R. H. (1949). "Oleyl alcohol". Organic Syntheses. 29: 80. doi:10.15227/orgsyn.029.0080.
Ford, S. G.; Marvel, C. S. (1930). "Lauryl Alcohol". Organic Syntheses. 10: 62. doi:10.15227/orgsyn.010.0062.
R. H. Manske (1934). "Decamethylene Glycol". Organic Syntheses. 14: 20. doi:10.15227/orgsyn.014.0020.
Whitmore, Frank C.; Otterbacher, T. (1930). "2-Heptanol". Organic Syntheses. 10: 60. doi:10.15227/orgsyn.010.0060.
Bodnar, Brian S.; Vogt, Paul F. (2009). "An Improved Bouveault-Blanc Ester Reduction with Stabilized Alkali Metals". J. Org. Chem. 74 (6): 2598–2600. doi:10.1021/jo802778z. PMID 19219971.
An, Jie; Work, D. Neil; Kenyon, Craig; Procter, David J. (2014). "Evaluating a Sodium Dispersion Reagent for the Bouveault–Blanc Reduction of Esters". J. Org. Chem. 79 (14): 6743–6747. doi:10.1021/jo501093g. PMID 24941291.
Han, Minhui; Ma, Xiaodong; Yao, Shangchu; Ding, Yuxuan; Yan, Zihan; Adijiang, Adila; Wu, Yufei; Li, Hengzhao; Zhang, Yuntong; Lei, Peng; Ling, Yun; An, Jie (2017). "Development of a Modified Bouveault–Blanc Reduction for the Selective Synthesis of α,α-Dideuterio Alcohols". J. Org. Chem. 82 (2): 1285–1290. doi:10.1021/acs.joc.6b02950. PMID 28029787.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Bodnar, Brian S.; Vogt, Paul F. (2009). "An Improved Bouveault-Blanc Ester Reduction with Stabilized Alkali Metals". J. Org. Chem. 74 (6): 2598–2600. doi:10.1021/jo802778z. PMID 19219971.
An, Jie; Work, D. Neil; Kenyon, Craig; Procter, David J. (2014). "Evaluating a Sodium Dispersion Reagent for the Bouveault–Blanc Reduction of Esters". J. Org. Chem. 79 (14): 6743–6747. doi:10.1021/jo501093g. PMID 24941291.
Han, Minhui; Ma, Xiaodong; Yao, Shangchu; Ding, Yuxuan; Yan, Zihan; Adijiang, Adila; Wu, Yufei; Li, Hengzhao; Zhang, Yuntong; Lei, Peng; Ling, Yun; An, Jie (2017). "Development of a Modified Bouveault–Blanc Reduction for the Selective Synthesis of α,α-Dideuterio Alcohols". J. Org. Chem. 82 (2): 1285–1290. doi:10.1021/acs.joc.6b02950. PMID 28029787.

Bouveault–Blanc reduction (English Wikipedia)

bnf.fr (Global: 124th place; English: 544th place)

gallica.bnf.fr

doi.org (Global: 2nd place; English: 2nd place)

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

bnf.fr (Global: 124^th place; English: 544^th place)

doi.org (Global: 2^nd place; English: 2^nd place)

nih.gov (Global: 4^th place; English: 4^th place)