Stereoselective Reduction of α-Iodospirolactones. Total Synthesis of (+/-)-Liguloxide.

DOI: 10.1016/S0040-4039(00)61015-8

Source and publish data:

Tetrahedron Letters p. 6673 - 6676 (1992)

Update date:2022-07-30

Topics:

Authors:

Lee, Eun

Lee, Dae Sung

Choi, Yoon Whan

Lee, Kwang Ho

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

Article abstract of DOI:10.1016/S0040-4039(00)61015-8

Radical-mediated reduction of α-methyl-α-iodospirolactones yielded trans-α-methylspirolactones selectively.This reaction was used in the total synthesis of (+/-)-liguloxide.

Full text of DOI:10.1016/S0040-4039(00)61015-8

Products guided by the article

Product name:2H-3,9a-Methanocyclopent[b]oxocin,octahydro- 2,2,6,9-tetramethyl-,(3R,6R,6aR,9S,9aS)-

Cas No:33784-90-6

R&D Labs maybe for 33784-90-6

Lanzhou SchiffChem Co.,Ltd

Contact:86-931-8272767

Address:Room 602, No.461, Nanchang Road, Chengguan District, Lanzhou City, China PRC
Jinhua City Mingzhu Pharmaceutical Co.,Ltd.

Contact:15857995878 0579-82207761

Address:No.169 Shenze Road, New Area,Jinpan Development Zone, Jinhua
Wuhan HengHeDa Pharm Co., Ltd

Contact:86-27-84888681

Address:Wuhan economic & technology development zone
Changzhou Yongxu Chemical Co.,Ltd

Contact:86-0519-85286591

Address:Room 1812,Wanda Plaza B,Xinbei District,Changzhou,Jiangsu,China
A.M FOOD CHEMICAL CO., LIMITED

Contact:86-531-87100375

Address:20Floor，Bblock，1Building，pharma-valley，Jinan，China

Relevant to this article

Doi:10.1021/jo00976a030
(1972)
Synthesis and antibacterial activity of new 4″-O-carbamates of 11,12-cyclic carbonate erythromycin A 6,9-imino ether

Doi:10.1038/ja.2010.166
(2011)
Doi:10.1016/S0031-9422(00)89893-3
(1971)
Doi:10.1021/j100691a007
(1971)
Rh(ii)-catalyzed cycloadditions of 1-tosyl 1,2,3-triazoles with 2H-azirines: Switchable reactivity of Rh-azavinylcarbene as [2C]- or aza-[3C]-synthon

Doi:10.1039/c5cc00268k
(2015)
A Mild and Efficient Method for Semmler-Wolff Aromatization; A Versatile Route to m-Alkoxy-, m-Halogeno-, and m-Thiocyanato-acetanilides

Doi:10.1055/s-1980-29253
(1980)

Article Doi