6-cloro-1-hexino (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "6-cloro-1-hexino" in Spanish language version.

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acros.com

ukpai-acrext-p1.acros.com

6-Chloro-1-hexyne. MSDS (Thermo Fisher)

acs.org

pubs.acs.org

Taylor, W.R.; Strong, F.M. (1950). «Synthesis of Unsaturated Fatty Acids». J. Am. Chem. Soc. 72 (9): 4263-4265. Consultado el 13 de febrero de 2020.

chemicalbook.com

6-Chloro-1-hexyne (Chemical Book)

chemspider.com

6-Chloro-1-hexyne (ChemSpider)

chemsrc.com

6-Chloro-1-hexyne (ChemSrc)

nih.gov

pubchem.ncbi.nlm.nih.gov

6-Chloro-1-hexyne (PubChem)

nist.gov

webbook.nist.gov

Número CAS

patents.google.com

Method for producing a conjugated Z-alken-yn-yl acetate (2014) Yamashita, M.; Fukumoto, T.; Kinsho, T. Patente US9376368B2

springer.com

link.springer.com

Lenin, H.H., Lauro, F.V., Marcela, R.N. et al. (2017). «Design and synthesis of an indol derivative as antibacterial agent against Staphylococcus aureus». Journal of Chemical Biology 10 (4): 159-177. Consultado el 13 de febrero de 2020.

thieme.com

science-of-synthesis.thieme.com

Lawrence, S.A. (2009). «40.1.1.5.4.3.2 Method 2: Reactions of Primary, Secondary, or Tertiary Amines with Alkyl Halides». Science of Synthesis 40: 526. Consultado el 2 de enero de 2019.
Kauffman, M. C.; Walsh, P. J (2011). «2.9.2.1.1 Alkenylation with Organozinc Reagents through Hydroboration–Transmetalation of Alkynes». Science of Synthesis: Stereoselective Synthesis 2: 475. Consultado el 13 de febrero de 2020.
Aitken, R. A.; Aitken, K. (2008). «43.8.3.1.7.2 Variation 2: With a Bromoalkane». Science of Synthesis 43: 601. Consultado el 13 de febrero de 2020.