Aziridine-2,3-diones

DOI: 10.1021/ja00542a065

Source and publish data:

Journal of the American Chemical Society p. 6902 - 6903 (1980)

Update date:2022-08-05

Topics:

Authors:

Aoyama, Hiromu

Sakamoto, Masami

Omote, Yoshimori

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

Article abstract of DOI:10.1021/ja00542a065

Full text of DOI:10.1021/ja00542a065

Products guided by the article

Product name:3-Methyl-1,5-diphenyl-6,7,8-trioxa-3-aza-bicyclo[3.2.1]octane-2,4-dione

Cas No:75693-09-3

R&D Labs maybe for 75693-09-3

Rudong Zhenfeng Yiyang Chemical Co., Ltd.

Contact:0513-84573047

Address:South Fengli Town, Rudong County, Jiangsu Province, China
King Brother Chem Co., Ltd

website:http://www.uvchemkeys.com

Contact:0086-021-58785816

Address:RM2607 Building No.1 Guosheng, Lane 388, Zhongjiang Road, Putuo District, Shanghai 200062 China
Zouping Mingxing Chemical Co.,Ltd.

website:http://www.zoutong.com.cn

Contact:86-543-2240068 2240067

Address:428 Daixi Third Road Zouping County Shandong Province China
Hangzhou Bayee Chemical Co.,Ltd.

Contact:+86-571-86990109

Address:No.380, Jiangnan Auenue, Binjiang District, Hangzhou, China
Taizhou Chemedir Biopharm-tech Co., Ltd

Contact:+86 523 86200218

Address:G09, No. 1 Avenue China Medical City, Taizhou,Jiangsu, China

Relevant to this article

Doi:10.1021/ja01112a054
(1953)
Rhodamine-pyrene conjugated chemosensors for ratiometric detection of Hg²⁺ ions: Different sensing behavior between a spirolactone and a spirothiolactone

Doi:10.1016/j.dyepig.2013.02.019
(2013)
Synthesis of naphthalenediols by aerobic oxidation of diisopropylnaphthalenes catalyzed by N-hydroxyphthalimide (NHPI)/α, α′-azobisisobutyronitrile (AIBN)

Doi:10.1002/adsc.200303168
(2004)
Solvent-Assisted Oxy-Cope Rearrangement of Non-Conjugated Enynols; A New Efficient Synthesis of Pseudoionone and its Analogs

Doi:10.1055/s-1980-29157
(1980)
Design, synthesis, biological evaluation and molecular docking study of novel pyridoxine-triazoles as anti-Alzheimer's agents

Doi:10.1039/d0ra04942e
(2020)
Doi:10.1007/BF00565880
()

Article Doi