A Mild and Efficient Tris(pentafluorophenyl)borane-catalyzed Sakurai Allylation of N-Benzyloxycarbonylamino p-Tolylsulfone with Allyltrimethylsilane 


Vol. 33,  No. 4, pp. 1275-1278, Apr.  2012
10.5012/bkcs.2012.33.4.1275


PDF
  Tumbnail

  Abstract

Tris(pentafluorophenyl)borane, B(C6F5)3, was found to be an efficient catalyst for synthesis of N-Cbzhomoallylic amines using Sakurai allylation of N-benzyloxycarbonyl-amino p-tolylsulfones with allyltrimethylsilane.

  Statistics
Cumulative Counts from November, 2022
Multiple requests among the same browser session are counted as one view. If you mouse over a chart, the values of data points will be shown.


  Cite this article

[IEEE Style]

P. Thirupathi, L. N. Neupane, K. Lee, "A Mild and Efficient Tris(pentafluorophenyl)borane-catalyzed Sakurai Allylation of N-Benzyloxycarbonylamino p-Tolylsulfone with Allyltrimethylsilane," Bulletin of the Korean Chemical Society, vol. 33, no. 4, pp. 1275-1278, 2012. DOI: 10.5012/bkcs.2012.33.4.1275.

[ACM Style]

Ponnaboina Thirupathi, Lok Nath Neupane, and Keun-Hyeung Lee. 2012. A Mild and Efficient Tris(pentafluorophenyl)borane-catalyzed Sakurai Allylation of N-Benzyloxycarbonylamino p-Tolylsulfone with Allyltrimethylsilane. Bulletin of the Korean Chemical Society, 33, 4, (2012), 1275-1278. DOI: 10.5012/bkcs.2012.33.4.1275.

Search
(IN TITLE, AUTHOR, ABSTRACT,KEYWORDS)

Advanced Search ▼

POPULAR KEYWORDS
(TOP 10 KEYWORDS)

Recent Publications
(LAST 3 YEARS)

ISSN(Print) 0253-2964
ISSN(Online) 1229-5949