Markó–Lam deoxygenation (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Markó–Lam deoxygenation" in English language version.

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1organic-chemistry.org

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1lamresearchgroup.com

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bnf.fr

gallica.bnf.fr

Bouveault, L.; Blanc, G. L. (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.

chem-station.com

マルコ・ラム脱酸素化 Marko-Lam Deoxygenation – ODOOS -合成反応データベース- by Chem-Station. Chem-station.com (2010-06-06). Retrieved on 2014-01-28.

doi.org

Lam, K.; Markó, I.E. (2008). "Using toluates as simple and versatile radical precursors". Org. Lett. 10 (13): 2773–2776. doi:10.1021/ol800944p. PMID 18507394.
Lam, K.; Markó, I.E. (2009). "Organic electrosynthesis using toluates as simple and versatile radical precursors" (PDF). Chem. Commun. 2009 (1): 95–97. doi:10.1039/b813545b. PMID 19082010.
Lam, K.; Markó, I.E. (2009). "Chemoselective chemical and electrochemical deprotections of aromatic esters". Org. Lett. 11 (13): 2752–2755. doi:10.1021/ol900828x. PMID 19492803.
Lam, K.; Markó, I.E. (2009). "Toluates: Unexpectedly versatile reagents". Tetrahedron. 65 (52): 10930–10940. doi:10.1016/j.tet.2009.09.111.
Takahashi, K.; Akao, R. & Honda, T. (2009). "Efficient diastereoselective synthesis of trifarane-type sesquiterpenes, trifarienols A and B". J. Org. Chem. 74 (9): 3424–3429. doi:10.1021/jo900369t. PMID 19334700.

gre.ac.uk

gala.gre.ac.uk

Lam, K.; Markó, I.E. (2009). "Organic electrosynthesis using toluates as simple and versatile radical precursors" (PDF). Chem. Commun. 2009 (1): 95–97. doi:10.1039/b813545b. PMID 19082010.

lamresearchgroup.com

"Home". lamresearchgroup.com.

nih.gov

pubmed.ncbi.nlm.nih.gov

Lam, K.; Markó, I.E. (2008). "Using toluates as simple and versatile radical precursors". Org. Lett. 10 (13): 2773–2776. doi:10.1021/ol800944p. PMID 18507394.
Lam, K.; Markó, I.E. (2009). "Organic electrosynthesis using toluates as simple and versatile radical precursors" (PDF). Chem. Commun. 2009 (1): 95–97. doi:10.1039/b813545b. PMID 19082010.
Lam, K.; Markó, I.E. (2009). "Chemoselective chemical and electrochemical deprotections of aromatic esters". Org. Lett. 11 (13): 2752–2755. doi:10.1021/ol900828x. PMID 19492803.
Takahashi, K.; Akao, R. & Honda, T. (2009). "Efficient diastereoselective synthesis of trifarane-type sesquiterpenes, trifarienols A and B". J. Org. Chem. 74 (9): 3424–3429. doi:10.1021/jo900369t. PMID 19334700.

organic-chemistry.org

"Alkane synthesis by deoxygenation". Organic-chemistry.org. Retrieved 2010-01-01.