Stereospecific functionalization of (R)-(-)-1,1'-BI-2-naphthol triflate

DOI: 10.1016/S0040-4039(00)97053-9

Source and publish data:

Tetrahedron Letters p. 6321 - 6324 (1990)

Update date:2022-08-24

Topics:

Authors:

Kurz Kurz

Lee Lee

Morgans Jr.

Waldyke Waldyke

Ward Ward

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

Article abstract of DOI:10.1016/S0040-4039(00)97053-9

Several examples of transition metal mediated functionalization of chiral 1,1'-bi-2-naphthol triflate are described which proceed with complete retention of substrate chirality. The transformation described demonstrate the potential of Pd(0) mediated reactions for the stereoselective transformation of the C-O bonds in this substrate.

Full text of DOI:10.1016/S0040-4039(00)97053-9

Products guided by the article

Product name:(R)-2-diphenylphosphinyl-2'-trifluoromethanesulfonyloxy-1,1'-binaphthalene

Cas No:132532-04-8

R&D Labs maybe for 132532-04-8

Shandong Loyal Chemical industrial Co.,Ltd

Contact:0533-7451788

Address:Linzi Chemical Industrial Park, Zibo, Shandong Province
Nanjing Ruizhi Industry & Technologh Co.，Ltd.

Contact:+86-25-86808110

Address:441-4-A5,NO.12 Longzang Avenue,Yuhuatai District,210039,Nanjing
SHANDONG QINGYUNCHANGXIN CHEMICAL SCIENCE-TECH CO.,LTD

Contact:86-21-60560171

Address:1689Donghuan Rade,Qingyun County, Dezhou City, Shandong,China
Zhejiang Chemicals Import & Export Corporation

Contact:86-571-87043088

Address:No.37,Qingchun Road,Hangzhou,China
Zhejiang Quzhou Zhengbang Organosilicon Co.,ltd.

Contact:86-570-3375195

Address:No.17 Lingqing Road technology industry,Quzhou City,Zhejiang Province,China

Relevant to this article

Doi:10.1002/jlcr.2590060210
(1970)
Doi:10.1007/BF01554635
()
SYNTHESIS OF NEW UNSATURATED ESTERS, CATALYZED BY PALLADIUM-PHOSPHINE COMPLEXES

Doi:10.1016/S0040-4039(01)80405-6
(1989)
Synthesis of N,N′-disubstituted urea from ethylene carbonate and amine using CaO

Doi:10.1246/cl.2004.742
(2004)
Enthalpies of combustion of 1,4-naphthoquinone, 9,10-anthraquinone, 9,10-phenanthraquinone, 1,4,9,10-anthradiquinone, 5,8-dihydroxy-1,4-naphthoquinone, and 1,4-dihydroxy-9,10-anthraquinone

Doi:10.1016/0021-9614(89)90016-5
(1989)
Design, synthesis, molecular docking, and some metabolic enzyme?inhibition properties of novel quinazolinone derivatives

Doi:10.1002/ardp.202000455
(2021)

Article Doi