Follow the Silyl Cation: Insights into the Vorbrüggen Reaction-Reference-Cited by-同舟云学术

Follow the Silyl Cation: Insights into the Vorbrüggen Reaction

Published:2019-08-21 Issue:9 Volume:23 Page:2050-2056
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Beutner Gregory L.¹^ORCID,Bultman Michael S.¹^ORCID,Cohen Benjamin M.¹^ORCID,Fan Junying¹,Marshall Jonathan¹,Sfouggatakis Chris¹

Affiliation:

1. Chemical and Synthetic Development, Bristol-Myers Squibb Company, One Squibb Drive, New Brunswick, New Jersey 08903, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.9b00304

Reference31 articles.

1. aSweeney, J.; Perkins, G.; Aguilar, E.; Fernandez-Rodriguez, M. A. In Handbook of Reagents for Organic Synthesis: Reagents for Silicon-Mediated Organic Synthesis; Fuchs, P., Ed. John Wiley & Sons, Ltd.: Chichester, UK, 2011; pp 518–537.

2. bHosomi, A.; Miura, K. In Lewis Acid Reagents; Yamamoto, H., Ed. Oxford University Press: Oxford, UK, 1999; pp 159–168.

3. Trimethylsilyl trifluoromethanesulfonate (TMSOTf) andN,N-di-iso-propyl ethyl amine (Hünig base): an effective reagent combination for selective silylation and elimination reactions

4. Synthesis Of Nucleosides

5. Nitrogen Glycosylation Reactions Involving Pyrimidine and Purine Nucleoside Bases with Furanoside Sugars

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