Diastereoselective trifluoromethylation of chiral imide enolates with iodotrifluoromethane mediated by triethylborane

DOI: 10.1016/0957-4166(94)80046-4

Source and publish data:

Tetrahedron Asymmetry p. 961 - 974 (1994)

Update date:2022-09-26

Topics: Diastereoselective Trifluoromethylation Triethylborane

Authors:

Iseki Iseki

Nagai Nagai

Kobayashi

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

Article abstract of DOI:10.1016/0957-4166(94)80046-4

The trifluoromethylation of lithium enolates of chiral N-acyloxazolidinones with iodotrifluoromethane mediated by triethylborane proceeds with good diastereomeric excess.

Full text of DOI:10.1016/0957-4166(94)80046-4

Products guided by the article

Product name:(2'R,4R)-3-(2'-benzyloxy-3',3',3'-trifluoropropionyl)-4-isopropyl-2-oxazolidinone

Cas No:165801-12-7

R&D Labs maybe for 165801-12-7

Hunan Shineway Enterprise Co., Ltd.

Contact:+86-731-86303875

Address:118, Huanghua International Airport Road, Huanghua Town, Changsha, Hunan 410137, China
HAORUI ENTERPRISES LLC

Contact:(1) 206-3550089

Address:5115 NE 8TH PL, Renton, WA 98059 USA
CHEM PLUS

Contact:0027-717-456976

Address:2ND FLOOR, 325 VAUSE ROAD, OVERPORT, 4001, SOUTH AFRICA
Shenyang Mole pharmaceutical Technology Development Co.,Ltd

Contact:+86-24-31204918/13889278616

Address:No.44, wanliutang road, shenhe District of Shenyang
Shandong Hongxiang Zinc Co., Ltd

Contact:086-0311-66187879

Address:DaWang developing zone

Relevant to this article

Chirality memory of α-methylene-π-allyl iridium species

Doi:10.1039/d1sc02636d
(2021)
Metal-Free [2 + 2 + 2] Cycloaddition of Ynamide-Nitriles with Ynamides: A Highly Regio- and Chemoselective Synthesis of δ-Carboline Derivatives

Doi:10.1021/acs.joc.8b02112
(2018)
Doi:10.1021/jo01272a035
(1968)
Structure of Phosphorus-Containing Peptide Ligands. X-ray and NMR Structural Study of Free Ligand and Rhodium Complex

Doi:10.1021/jo970773e
(1997)
Doi:10.1021/ja01490a071
(1960)
Novel thiosemicarbazide derivatives with 4-nitrophenyl group as multi-target drugs: α-glucosidase inhibitors with antibacterial and antiproliferative activity

Doi:10.1016/j.biopha.2017.07.049
(2017)

Article Doi