PHOTOLYSIS STUDIES OF α-DIAZOAMIDES. THE EFFECT OF CARBOXAMIDE SUBSTITUENTS ON SELECTIVITY RATIOS

DOI: 10.1016/S0040-4039(00)81373-8

Source and publish data:

Tetrahedron Letters p. 233 - 236 (1983)

Update date:2022-08-16

Topics:

Authors:

Wydila, John

Thornton, Edward R.

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

Article abstract of DOI:10.1016/S0040-4039(00)81373-8

Photolysis of several α-diazoamide compounds in mixed solvent systems has resulted in unusually large OH:CH insertion selectivity ratios of 10³-10⁴:1.

Full text of DOI:10.1016/S0040-4039(00)81373-8

Products guided by the article

Product name:2-tert-Butoxy-N-cyclohexyl-acetamide

Cas No:85971-12-6

R&D Labs maybe for 85971-12-6

SHANXI JINJIN CHEMICAL INDUSTRIAL CO.,LTD

website:http://www.jinjingroup.com

Contact:4009982989

Address:Economic And Technological Development Zone,Hejin?City,Shanxi Province?,China
Weifang Arylchem Chemical Co., LTD

Contact:86-536-5217866

Address:Development Zone, Shouguang, Shandong Province
Hangzhou Cherry Pharmaceutical Technology Co., Ltd.

Contact:+86 (571) 8163-6070 / +86 18042403330

Address:262Wangtang Road
Guangzhou PI & PI Biotech Inc. Ltd.

Contact:+86-20-81716320

Address:Suite 501,198 Kaiyuan Ave.,Science City, Guangzhou,China
waho int'l company

Contact:+86-579-85206992

Address:No 451 chouzhou north road ,room 1106 int'l business center , yiwu ,china

Relevant to this article

THE METHOXYCARBONYLALKYLATION AND METHOXYCARBONYLALKYLIDENATION OF SILYL ENOL ETHERS

Doi:10.1016/S0040-4039(00)81397-0
(1983)
Doi:10.1021/ja01307a054
(1935)
Type III-C rotaxane dendrimers: Synthesis, dual size modulation and: In vivo evaluation

Doi:10.1039/c9cc06200a
(2019)
Doi:10.1039/jr9530001241
(1953)
Doi:10.1039/jr9460001052
(1946)
Doi:10.1021/ja01299a005
(1936)

Article Doi