A Useful Route to Optically Active 4-Oxygenated 4,5-Dihydroisoxazoles

DOI: 10.1021/jo00103a007

Source and publish data:

Journal of Organic Chemistry p. 7199 - 7200 (1994)

Update date:2022-07-30

Topics:

Authors:

Wade, Peter A.

Shah, Sharmila S.

Govindarajan, Lakshmi

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

Article abstract of DOI:10.1021/jo00103a007

Optically active iodotosylates were prepared from carbohydrate precursors and were transformed by the action of excess sodium nitrite/propyl nitrite to bicyclic 4-oxygenated 4,5-dihydro-3-nitroisoxazoles.

Full text of DOI:10.1021/jo00103a007

Products guided by the article

Product name:C₄₀H₄₀O₁₀S₂

Cas No:69649-64-5

R&D Labs maybe for 69649-64-5

Ningbo Huajia Chemicals

Contact:+86-574-87065746

Address:10th Floor, No.787 Baizhang East Road,
Xinchang Jiu Xin Pharmaceutical Co., Ltd

website:http://www.jiuxinpharm.com

Contact:86 137 5756 8585

Address:Poyang industry Park
Xiamen Huasing Chemicals Co.Ltd.

Contact:0086-592-6228397

Address:NO.24, Xinglin North 2nd Road,Jimei district
Golden Union Agrochemical Import and Export Co., Ltd.

Contact:86-755-23910527

Address:Room 1106, Tower 3A, Excellence Century Center, Futian District, Shenzhen, China
Synochem Ingredients Corp., Ltd.

Contact:+86-512-5636 2180

Address:Zhangjiagang Free Trade Zone

Relevant to this article

SYNTHESE D'ALCOHOLS α-ALLENIQUES PAR REACTION D'ORGANOCHROMIQUES PROPARGYLIQUES SUR LES ALDEHYDES ET LES CETONES

Doi:10.1016/S0040-4020(01)92452-4
(1981)
A NOVEL ROUTE TO ALDEHYDIC ENOL ETHERS AND ENAMINES

Doi:10.1016/S0040-4039(00)71480-8
(1980)
Molecular tectonics - Use of urethanes and ureas derived from tetraphenylmethane and tetraphenylsilane to build porous chiral hydrogen-bonded networks

Doi:10.1139/v03-208
(2004)
Tetracycle formation from the reaction of acetophenones with 1-aminoanthraquinone, and further annulation of pyridine and diazepine rings

Doi:10.1071/CH03136
(2003)
Total synthesis of monensin. 2. Stereocontrolled synthesis of the right half of monensin

Doi:10.1021/ja00495a065
(1979)
Total Synthesis of Antiproliferative Parvifloron F

Doi:10.1021/acs.orglett.7b03763
(2018)

Article Doi