Absolute stereostructure of swinholide A, a potent cytotoxic macrolide from the Okinawan marine sponge Theonella swinhoei

DOI: 10.1021/ja00165a094

Source and publish data:

Journal of the American Chemical Society p. 3710 - 3712 (1990)

Update date:2022-08-02

Topics:

Authors:

Kitagawa

Kobayashi

Katori Katori

Yamashita

Tanaka Tanaka

Doi Doi

Ishida Ishida

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

Article abstract of DOI:10.1021/ja00165a094

Full text of DOI:10.1021/ja00165a094

Products guided by the article

Product name:C₆₂H₉₂Br₂O₁₆

Cas No:131702-03-9

R&D Labs maybe for 131702-03-9

JIANGXI AIFEIMU TECHNOLOGY CO.，LTD

Contact:+86-570-6040289

Address:FINECHEMICAL PARK,ZIBU TOWN,WANNIAN COUNTY,JIANGXI PROV.,CHINA,ZIP
ZHEJIANG NHU COMPANY LTD.

Contact:86-575-86132822，86-575-86085355

Address:No.418 Dadao West Road,Qixing Street,Xinchang, Zhejiang Province, China.
ZCIC INTERNATIONAL LTD

Contact:+86-512-56795332

Address:No227 Shuanglong Rd, Fenghuang, Zhangjiagang
Haitong Chemical Industrial Co.,Ltd.

website:https://www.haitonglongwin.com/

Contact:+86-022-66221018

Address:18-701, No.99, The 4th Street, TEDA,
Shanghai PengMo Biotechnology Co.,Ltd

website:http://www.pengmobio.lookchem.com

Contact:86-13052359378

Address:No.218 Hai Qu Road.Shanghai.China

Relevant to this article

Palladium(II)-catalyzed cycloisomerization of functionalized 1,5-hexadienes

Doi:10.1021/ol201795w
(2011)
First asymmetric cascade reaction catalysed by chiral primary aminoalcohols

Doi:10.1039/c1ob05400g
(2011)
Radical-Triggered Tandem Cyclization of 1,6-Enynes with H₂O: A Way to Access Strained 1 H-Cyclopropa[ b]naph thalene-2,7-diones

Doi:10.1021/acs.orglett.8b03007
(2018)
Ladder-type P,S-bridged trans-stilbenes

Doi:10.1021/ic201116p
(2011)
Synthesis and Evaluation of Novel Ether Lipid Nucleoside Conjugates for Anti-HIV-1 Activity

Doi:10.1021/jm00108a025
(1991)
Directing Group Participated Benzylic C(sp³)-H/C(sp²)-H Cross-Dehydrogenative Coupling (CDC): Synthesis of Azapolycycles

Doi:10.1021/acs.orglett.7b03748
(2018)

Article Doi