Scholarly article on 2-Hexenoic acid, 6-(2-methyl-3-phenyl-2H-azirin-2-yl)-, methyl ester, (E)- 62901-88-6 from Journal of the American Chemical Society p. 1871 - 1880

DOI: 10.1021/ja00448a031

Source and publish data:

Journal of the American Chemical Society p. 1871 - 1880 (1977)

Update date:2022-08-04

Topics:

Authors:

Padwa,A.

Kamigata,N.

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

Article abstract of DOI:10.1021/ja00448a031

Full text of DOI:10.1021/ja00448a031

Products guided by the article

Product name:2-Hexenoic acid, 6-(2-methyl-3-phenyl-2H-azirin-2-yl)-, methyl ester, (E)-

Cas No:62901-88-6

R&D Labs maybe for 62901-88-6

Henan Techway Chemical Co.,Ltd.

website:http://www.techwaychem.com

Contact:+86-371-66380080

Address:No.27 Shunhe Road,
Rudong Zhenfeng Yiyang Chemical Co., Ltd.

Contact:0513-84573047

Address:South Fengli Town, Rudong County, Jiangsu Province, China
Evershine Chemical CO Ltd

Contact:+86-571-87010026

Address:202, Zhenhua Road,
WUHAN WELLSONG INT'L CO.,LTD

Contact:+86-27-85733560

Address:NO.308,QINGNIAN RD.,WUHAN,CHINA
Shandong Shouguang Songchuan Industrial Additives Co.,Ltd

Contact:+86-536-8566856

Address:Shouguang,Shandong,China

Relevant to this article

Useful Enantioselective Bicyclization Reactions Using an N-Protonated Chiral Oxazaborolidine as Catalyst

Doi:10.1021/ol035542a
(2003)
Synthesis of stable isotope-labeled precursors for the biosyntheses of capsaicinoids, capsinoids, and capsiconinoids

Doi:10.1271/bbb.110187
(2011)
Intramolecular Nucleophilic Substitution by Phosphinate and Thiophosphinate Anions: Relative Rates of Formation of Five- and Six-membered Rings

Doi:10.1039/c39950000083
(1995)
Synthesis of Carbapenems Containing Peptidoglycan Mimetics and Inhibition of the Cross-Linking Activity of a Transpeptidase of l,d Specificity

Doi:10.1002/chem.202004831
(2021)
SUCRES ACETYLENIQUES HETEROSUBSTITUES SUR LA TRIPLE LIAISON

Doi:10.1016/S0008-6215(00)80850-2
(1981)
Bioinspired Syntheses of the Pyridoacridine Marine Alkaloids Demethyldeoxyamphimedine, Deoxyamphimedine, and Amphimedine

Doi:10.1021/acs.joc.5b02312
(2016)

Article Doi

DOI: 10.1021/ja00448a031