+++acs+els

[Maloy]

Скачайте пожалуйста статьи:
1. Synthetic methods and reactions. 141. Fluoride-induced trifluoromethylation of carbonyl compounds with trifluoromethyltrimethylsilane (TMS-CF3). A trifluoromethide equivalent
G. K. Surya Prakash, Ramesh Krishnamurti, George A. Olah
JACS 1989, 111, 393–395

Код: Выделить всё

http://dx.doi.org/10.1021/ja00183a073

2. Die ersten CF3-substituierten organyl(chlor)silane
Ingo Ruppert, Klaus Schlich, Wolfgang Volbach
Tetrahedron Letters, Volume 25, Issue 21, 1984, Pages 2195-2198

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4039(01)80208-2

3. A new method for synthesis of trifluoromethyl-substituted phenols and anilines
G. Patrick Stahly, Donald R. Bell
JOC, 1989, 54, 2873–2877

Код: Выделить всё

http://dx.doi.org/10.1021/jo00273a020

4. Quaternary ammonium enolates as synthetic intermediates. Trimethylsilylacetate: a new class of silylating reagent for ketones and alcohols
Eiichi Nakamura, Toshiaki Murofushi, Makoto Shimizu, Isao Kuwajima
JACS 1976, 98, 2346–2348

Код: Выделить всё

http://dx.doi.org/10.1021/ja00424a064

5. Flash thermolysis of aryl trifluoroacetates: A new approach to trifluoromethylated aromatic compounds
Y. Kobayashi, A. Nakazato, I. Kumadaki, R. Filler
Journal of Fluorine Chemistry, 32, 4, 1986, 467-470

Код: Выделить всё

http://dx.doi.org/10.1016/S0022-1139(00)81954-5

6. Tetrakis(dimethylamino)ethylene/trifluoroiodomethane. a specific novel trifluoromethylating agent
G. Pawelke
Journal of Fluorine Chemistry, 42, 3, 1989, 429-433

Код: Выделить всё

http://dx.doi.org/10.1016/S0022-1139(00)83934-2

7. Methods of Fluorination in Organic Chemistry
Michael R. C. Gerstenberger, Alois Haas
Angew. Chem. IE, 1981, 20, 647-667

Код: Выделить всё

http://dx.doi.org/10.1002/anie.198106471

8. Trialkylsily(trifluoromethyl)diazenes as Tailored Reagents for Nucleophilic Trifluoromethylation
Uwe Hartkopf, Armin de Meijere
Angew. Chem. IE, 1982, 21, 443

Код: Выделить всё

http://dx.doi.org/10.1002/anie.198204431

Большое спасибо за помощь!

[nikolay_ap]

2, 5 - 7

2.pdf

5.pdf

6.pdf

7.pdf

[nikolay_ap]

8

8.pdf

[nikolay_ap]

1

1.pdf

[nikolay_ap]

3, 4

jo00273a020.pdf

ja00424a064.pdf