Total Synthesis of 11-Deoxydaunomycinone

DOI: 10.1039/c39820000421

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 421 - 423 (1982)

Update date:2022-08-04

Topics:

Authors:

Gesson, Jean-Pierre

Mondon, Martine

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

Article abstract of DOI:10.1039/c39820000421

11-Deoxydaunomycinone (2), the aglycone of a recently isolated antitumor anthracycline, is prepared using two different routes in only seven and eight steps respectively.

Full text of DOI:10.1039/c39820000421

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:{Methoxy-[4-(2-methyl-[1,3]dithian-2-yl)-2-methylene-cyclohex-(E)-ylidene]-methoxy}-trimethyl-silane

Cas No:82792-74-3

R&D Labs maybe for 82792-74-3

Rizhao Lanxing Chemical Indusrial Co.,Ltd

Contact:86-633-2616708

Address:NO.15 West road Shenglan, Lanshan district, Rizhao City
Hangzhou Showland Technology Co., Ltd.

Contact:86-571-88920516

Address:ROOM2118,NO.553,WENSAN ROAD,HANGZHOU,CHINA
Jiangsu Institute of Ecomones Co., Ltd

website:http://www.jsmone.com

Contact:+86-519-82821700

Address:95 Huanyuan N. Road, Jintan, Jiangsu, China
AURORA CHEMICAL CO., LTD

Contact:86-532-68629711 13780605697

Address:NO 220 YANAN 3 ROAD,(POST ADMINISTRATION BUILDING),QINGDAO,CHINA
Nanjing HuiBaiShi Biotechnology Co.,Ltd.

Contact:+86 (25)58745219

Address:No.606 Ningliu Road,LiuHe District.

Relevant to this article

Synthesis of some bifunctional derivatives of 8-methylquinoline-5-carboxylic acid

Doi:10.1007/BF00506150
(1982)
STRUCTURE AND ANOMERIC CONFIGURATION OF THE C-NUCLEOSIDE ANALOGS OBTAINED BY DEHYDRATION OF 7-DEOXY-L-manno-2-HEPTULOSE PHENYLOSAZONE

Doi:10.1016/S0008-6215(00)80733-8
(1982)
Ammonia Activation by Sc⁺ and Ti⁺: Electronic and Translational Energy Dependence

Doi:10.1021/j100370a051
(1990)
Synthesis and bioactivities of pyrazoline benzensulfonamides as carbonic anhydrase and acetylcholinesterase inhibitors with low cytotoxicity

Doi:10.1016/j.bioorg.2018.12.028
(2019)
Doi:10.1002/hlca.19590420513
(1959)
Studies on the constituents of Iris florentina L. II. C-glucosides of xanthones and flavones from the leaves

Doi:10.1248/cpb.30.2342
(1982)

Article Doi