Trimethylsilyl trifluoromethanesulfonate (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Trimethylsilyl trifluoromethanesulfonate" in English language version.

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8doi.org

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1acs.org

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1worldcat.org

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1semanticscholar.org

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1nih.gov

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acs.org

pubs.acs.org

Barber, Thomas; Argent, Stephen P.; Ball, Liam T. (2020-05-15). "Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di- tert -alkylphosphine Surrogates". ACS Catalysis. 10 (10): 5454–5461. doi:10.1021/acscatal.0c01414. ISSN 2155-5435. S2CID 219017552.

doi.org

Joseph Sweeney; Gemma Perkins; Enrique Aguilar; Manuel A. Fernández-Rodríguez; Rodolfo Marquez; Eric Amigues; Ricardo Lopez-Gonzalez (2018). "Trimethylsilyl Trifluoromethanesulfonate". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rt338. ISBN 978-0-471-93623-7.
Boeckman, Robert; Tusch, Douglas J.; Biegasiewicz, Kyle F. (2015). "(S)-1,1-Diphenylprolinol Trimethylsilyl Ether". Organic Syntheses. 92: 309–319. doi:10.15227/orgsyn.092.0309.
Umemoto, Teruo; Tomita, Kyoichi; Kawada, Kosuke (1990). "N-Fluoropyridinium Triflate: An Electrophilic Fluorinating Agent". Organic Syntheses. 69: 129. doi:10.15227/orgsyn.069.0129.
Efficient Stereoselective Synthesis of Proanthocyanidin Trimers with TMSOTf-Catalyzed Intermolecular Condensation. Akiko Saito, Akira Tanaka, Makoto Ubukata and Noriyuki Nakajima, Synlett, 2004, volume 6, pages 1069-1073, doi:10.1055/s-2004-822905
Love, Kerry R.; Seeberger, Peter H. (2005). "Synthesis and Use of Glycosyl Phosphates as Glycosyl Donors". Organic Syntheses. 81: 225. doi:10.15227/orgsyn.081.0225.
Barber, Thomas; Argent, Stephen P.; Ball, Liam T. (2020-05-15). "Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di- tert -alkylphosphine Surrogates". ACS Catalysis. 10 (10): 5454–5461. doi:10.1021/acscatal.0c01414. ISSN 2155-5435. S2CID 219017552.
Kuehne, Martin E.; Xu, Feng (1 December 1998). "Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. 10. An Enantioselective Synthesis of (−)-Strychnine through the Wieland−Gumlich Aldehyde". The Journal of Organic Chemistry. 63 (25): 9427–9433. doi:10.1021/jo9813989.
Doi, Takayuki; Numajiri, Yoshitaka; Munakata, Asami; Takahashi, Takashi (1 February 2006). "Total Synthesis of Apratoxin A". Organic Letters. 8 (3): 531–534. doi:10.1021/ol052907d. PMID 16435877.

nih.gov

pubmed.ncbi.nlm.nih.gov

Doi, Takayuki; Numajiri, Yoshitaka; Munakata, Asami; Takahashi, Takashi (1 February 2006). "Total Synthesis of Apratoxin A". Organic Letters. 8 (3): 531–534. doi:10.1021/ol052907d. PMID 16435877.

semanticscholar.org

api.semanticscholar.org

Barber, Thomas; Argent, Stephen P.; Ball, Liam T. (2020-05-15). "Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di- tert -alkylphosphine Surrogates". ACS Catalysis. 10 (10): 5454–5461. doi:10.1021/acscatal.0c01414. ISSN 2155-5435. S2CID 219017552.

worldcat.org

search.worldcat.org

Barber, Thomas; Argent, Stephen P.; Ball, Liam T. (2020-05-15). "Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di- tert -alkylphosphine Surrogates". ACS Catalysis. 10 (10): 5454–5461. doi:10.1021/acscatal.0c01414. ISSN 2155-5435. S2CID 219017552.