Scholarly article on p-Dodecyloxy-α-methylstyrol 70165-66-1 from Journal of the American Chemical Society p. 1896 - 1898

DOI: 10.1021/ja00501a053

Source and publish data:

Journal of the American Chemical Society p. 1896 - 1898 (1979)

Update date:2022-08-16

Topics:

Authors:

Menger,F.M.

Jerkunica,J.M.

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

Article abstract of DOI:10.1021/ja00501a053

Full text of DOI:10.1021/ja00501a053

Products guided by the article

Product name:p-Dodecyloxy-α-methylstyrol

Cas No:70165-66-1

R&D Labs maybe for 70165-66-1

Jinhua Haoyuan Chemical CO., LTD(expird)

Contact:86-579-82465583

Address:Jinhua,Zhejiang
xujianqiang

Contact:86-21-57725962

Address:shanghai
Fuxin Jintelai Fluorin Chemical Co., Ltd.

Contact:+86-0418-8229599

Address:, 7th Huagong Road, Fluorine industry development zone (Yimatu Town,Fumeng County),Fuxin City, Liaoning Province, China
Hangzhou Haiqiang Chemical Co.,Ltd.

Contact:+86-571-86960370

Address:Add: 5/F, Around Town North Road,No. 10, Hangzhou, Zhejiang,China
Shanghai Surseechem Co.,Ltd.

Contact:+86-21-61318535

Address:Building 29,No.2139 Xizha Road, Fengxian District, Shanghai

Relevant to this article

Probing crucial metabolic pathways in fungal pathogens of crucifers: Biotransformation of indole-3-acetaldoxime, 4-hydroxyphenylacetaldoxime, and their metabolites

Doi:10.1016/S0968-0896(03)00241-4
(2003)
A convenient synthesis of 2-amino-3-cyano-4-aryl-1,4,5,6-tetrahydrobenzo[h] chromenes derivatives using KF-Al₂O₃ as catalyst

Doi:10.1081/SCC-200030542
(2004)
Highly Efficient Iridium-Catalyzed Oxidation of Organosilanes to Silanols

Doi:10.1021/jo035647r
(2004)
SYNTHESIS OF 5,5'-DIHYDROXYLEUCINE AND 4-FLUORO-5,5'-DIHYDROXYLEUCINE, THE REDUCTION PRODUCTS OF 4-CARBOXYGLUTAMIC AND 4-CARBOXY-4-FLUOROGLUTAMIC ACIDS

Doi:10.1016/S0040-4020(01)80939-X
(1991)
Doi:10.1021/jo01329a008
(1979)
Suzuki cross-coupling reactions of γ-alkylidenebutenolides: Application to the synthesis of vulpinic acid

Doi:10.1021/jo049780a
(2004)

Article Doi

DOI: 10.1021/ja00501a053