A Sterospecific Synthesis of Highly Substituted Tetrahydrofurans

DOI: 10.1021/ja00414a088

Source and publish data:

Journal of the American Chemical Society p. 7398 - 7399 (1981)

Update date:2022-08-02

Topics:

Authors:

Williams, David R.

Phillips, James G.

Barner, Bruce A.

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

Article abstract of DOI:10.1021/ja00414a088

Full text of DOI:10.1021/ja00414a088

Products guided by the article

Product name:C₂₆H₃₀O₂S

Cas No:80091-18-5

R&D Labs maybe for 80091-18-5

YingYing Pharmaceutical Co.,Ltd

Contact:86-18854126208

Address:55#, yingxiongshan road
waho int'l company

Contact:+86-579-85206992

Address:No 451 chouzhou north road ,room 1106 int'l business center , yiwu ,china
Hubei Xiangxi Chemical Industry Co.,Ltd

Contact:+86-710-3454830

Address:No.7, Daqing East Road, Xiangfan City, Hubei Province, China
Taizhou Crene Biotechnology co.ltd

Contact:86-576-88813233 88205808

Address:Economic Developed Zone of Taizhou Zhejiang China
Changzhou Foreign Trade Corp

Contact:+86-519-86623222

Address:29F/D, 99 Yanling West Road, Changzhou, Jiangsu, China

Relevant to this article

Synthesis of fluoroalkyl vinyl sulfoxides and their use in Diels-Alder reactions

Doi:10.1055/s-2004-831201
(2004)
Stereoselective synthesis of highly substituted bicyclic γ-lactones using homoaldol addition of 1-(1-cycloalkenyl)methyl carbamates

Doi:10.1055/s-2004-831170
(2004)
Synthesis of 2-Substituted 3,4-Dihydro-1,2-diazepines by the Reactions of Unsaturated Ketones with Hydrazides

Doi:10.1039/P19810002761
(1981)
Synthesis of 1,3,5-triazines via Cu(OAc)₂-catalyzed aerobic oxidative coupling of alcohols and amidine hydrochlorides

Doi:10.1039/c5ob00724k
(2015)
Selective Electrochemical Reductive Acetylation of Aromatic Nitrosulfones

Doi:10.1021/jo00323a046
(1981)
Highly stereoselective 1,4-conjugate addition of organocopper reagents to methyl α-D-glucopyranoside derivatives tethering an unsaturated ester moiety at C-4 or C-6

Doi:10.1021/ol9909942
(1999)

Article Doi