Scholarly article on rac-6-methoxy-16.17-seco-estrapentaene-(1.3.5.7.9)-dioic acid-(16.17)-17-methyl ester 111497-69-9 from Journal of the American Chemical Society p. 2750,2752

DOI: 10.1021/ja01867a041

Source and publish data:

Journal of the American Chemical Society p. 2750,2752 (1940)

Update date:2022-07-28

Topics:

Authors:

Bachmann

Holmes Holmes

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

Article abstract of DOI:10.1021/ja01867a041

Full text of DOI:10.1021/ja01867a041

Products guided by the article

Product name:rac-6-methoxy-16.17-seco-estrapentaene-(1.3.5.7.9)-dioic acid-(16.17)-17-methyl ester

Cas No:111497-69-9

R&D Labs maybe for 111497-69-9

Dalian Synco Chemical Co., Ltd.

Contact:+86-411-83635150

Address:Rm 1004, 24, Tangshan Street, Dalian
Shanghai Coupling Pharmaceutical R&D Co., Ltd.(expird)

Contact:+86 021 50106671

Address:403 Room No.4 Buiding, No. 526 Ruiqing Road, Shanghai Zhangjiang Hi-Tech Park
HANGZHOU YUNUO CHEMICAL CO.,LTD

website:http://www.yunuochem.com

Contact:0571-83715115

Address:hangzhou
HAINAN JINYING IMPORT AND EXPORT CO. LTD

Contact:+86-898-32875423

Address:A SECTION 19TH FL, TIMES SQUARE, NO.2 GUO MAO AVENUE HAIKOU, HAINAN, P. R. OF CHINA
Jiangsu Jiuri Chemical Co.,Ltd.

Contact:+86-519-82118868

Address:Tianwang Town, Jurong City, Jiangsu Province, China

Relevant to this article

NUCLEOSIDES OF 4-METHYLTHIO-1,2,3-TRIAZOL-5-YL-CARBOXYLIC ACID DERIVATIVES

Doi:10.1007/BF00663860
(1987)
Matrix Isolation and Ultraviolet Spectra of Germylenes

Doi:10.1246/cl.1987.317
(1987)
Synthesis and spectroscopic investigations of 1,4-benzothiazepine derivatives

Doi:10.1139/v87-027
(1987)
Doi:10.1021/ja00211a020
(1988)
Synthesis of 2,2-Di-C-methyl-2-deoxy- and 4,4-Di-C-methyl-4-deoxypyranosides via Michael Addition of Conjugated Enopyranosiduloses

Doi:10.1246/bcsj.60.1433
(1987)
Competition between π-π Or furan-perfluorophenyl stacking interactions in conjugated compounds prepared from azomethine connections

Doi:10.1039/c1ce05575e
(2011)

Article Doi

DOI: 10.1021/ja01867a041