Esperamicins, a Novel Class of Potent Antitumor Antibiotics. 3. Structures of Esperamicins A1, A2, and A1b

DOI: 10.1021/ja00245a049

Source and publish data:

Journal of the American Chemical Society p. 3462 - 3464 (1987)

Update date:2022-07-29

Topics:

Authors:

Golik, Jerzy

Dubay, George

Groenewold, Gary

Kawaguchi, Hiroshi

Konishi, Masataka

et al. et al.

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

Article abstract of DOI:10.1021/ja00245a049

Full text of DOI:10.1021/ja00245a049

Products guided by the article

Product name:esperamicin D

Cas No:107473-04-1

R&D Labs maybe for 107473-04-1

Zhejiang Chemicals Import & Export Corporation (ZHECHEM)

Contact:+86-571-87046953

Address:No. 37, Qingchun Road
Beijing Green Guardee Technology CO,.LTD

Contact:+86-10-69706062

Address:F2 BLdj,5 No.37 Chaoqian Road
Shanghai Maxchemco Chemical Industry Co., Ltd.

Contact:(86)21-51079223

Address:No.1305-8, B241, the Ecust Park, Huajing Road, Xuhui District, Shanghai
ChangZhou Mascotchem. Co.,Ltd.

website:http://www.mascotchem.com

Contact:86-519-85010339

Address:B-802,XingBei Building,391#,Tongjiang Middle Road New District,Changzhou,JS,China
CHINA MEHECO CORPORATION

Contact:+86-10-67147360/67107388

Address:No.18 Guangming Zhongjie, Chongwen District, Beijing, 100061, China

Relevant to this article

Novel hypoglycemic dihydropyridones serendipitously discovered from O- versus C-alkylation in the synthesis of VMAT2 antagonists

Doi:10.1016/j.bmcl.2008.07.129
(2008)
Kagome type extra-large microporous solid based on a paddle-wheel Cu²⁺ dimer

Doi:10.1039/b806616g
(2008)
SYNTHESIS OF TWO HEXAPRENOLS MODIFIED WITH RESPECT TO POSITION OF HYDROXY GROUP

Doi:10.1007/BF00954019
(1986)
Oxo-ester mediated native chemical ligation: Concept and applications

Doi:10.1021/ja804993y
(2008)
Synthesis of D-rubranitrose and methyl α-D-tetronitroside by cyanomesylation of hexapyranosid-3-uloses

Doi:10.1016/S0008-6215(00)90152-6
(1986)
Efficient access to unprotected primary amines by iron-catalyzed aminochlorination of alkenes

Doi:10.1126/science.aat3863
(2018)

Article Doi