Ouverture des vinyloxiranes par le fluorhydrate de triethylamine triacide

DOI: 10.1016/0022-1139(94)03104-8

Source and publish data:

Journal of Fluorine Chemistry p. 141 - 144 (1995)

Update date:2022-09-26

Topics:

Authors:

Hedhli, A.

Baklouti, A.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0022-1139(94)03104-8

The action of triethylamine trihydrogen fluoride on vinyloxiranes leads, under mild conditions, to the corresponding fluorinated homoallylic alcohols.Some of these alcohols are unstable and accordingly have been converted into the corresponding more stabl

Full text of DOI:10.1016/0022-1139(94)03104-8

Products guided by the article

Product name:Toluene-4-sulfonic acid (E)-2-fluoro-3-methyl-pent-3-enyl ester

Cas No:161064-74-0

R&D Labs maybe for 161064-74-0

Afine Chemicals Limited

website:http://www.afinechem.com

Contact:+86-571-85134551

Address:No. 206 Zhen Hua Road, Hangzhou 310030, Zhejiang, China
Shaanxi HuaTai Bio-fine chemical company Ltd

Contact:86-029-87862197

Address:No. 5, 3rd Floor, 29 Yanta North Road, Beilin Dist.
Anhui Jiatiansen Agrochemical Co.,Ltd

Contact:15366811918

Address:chemical industrial park,xiangyu town,dongzhi county,anhui,china
Synochem Ingredients Corp., Ltd.

Contact:+86-512-5636 2180

Address:Zhangjiagang Free Trade Zone
Zibo Ocean International Trade Co.,Ltd(expird)

Contact:+86 533 5160706

Address:1117, Hongtai Bld., Songling rd, Zichuan,Zibo,Shandong,China

Relevant to this article

Alkaloid constituents from flower buds and leaves of sacred lotus (Nelumbo nucifera, Nymphaeaceae) with melanogenesis inhibitory activity in B16 melanoma cells

Doi:10.1016/j.bmc.2012.11.038
(2013)
The development of practical synthetic routes to a CB₂ agonist: Efficient construction of a densely substituted purine core

Doi:10.1021/op300278c
(2013)
Synthesis of the Tricyclic Nucleus of the Alkaloid Stemofoline: X-Ray Crystal Structure of (4RS,5RS,7SR,10RS)-10-Butyl-5-hydroxy-1-azatricyclo<5.3.0.0^4,10>decan-2-one

Doi:10.1039/c39920000538
(1992)
A chemical tuned strategy to develop novel irreversible EGFR-TK inhibitors with improved safety and pharmacokinetic profiles

Doi:10.1021/jm5014659
(2014)
Toll-like receptor-8 agonistic activities in C2, C4, and C8 modified thiazolo[4,5-c]quinolines

Doi:10.1039/c2ob26705e
(2013)
Discovery of novel N-substituted oxindoles as selective M₁ and M₄ muscarinic acetylcholine receptors partial agonists

Doi:10.1021/ml300372f
(2013)

Article Doi