A Total Synthesis of Antibacterial Clerodane, 16-Hydroxycleroda-3,13(14)Z-dien-15,16-olide

DOI: 10.1016/0040-4039(94)88279-7

Source and publish data:

Tetrahedron Letters p. 8189 - 8192 (1994)

Update date:2022-08-03

Topics:

Authors:

Hagiwara, Hisahiro

Inome, Kazuhiro

Uda, Hisashi

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

Article abstract of DOI:10.1016/0040-4039(94)88279-7

The total synthesis of an antibacterial clerodane, 16-hydroxycleroda-3,13(14)Z-dien-15,16-olide, is described and its absolute stereochemistry has been determined.

Full text of DOI:10.1016/0040-4039(94)88279-7

Products guided by the article

Product name:(4aR,5R,6R,8aR)-3,4,4a,5,6,7,8,8a-octahydro-5-(2'-triisopropylsiloxyethyl)-5,6,8a-trimethylnaphthalen-1(2H)-one

Cas No:161006-64-0

R&D Labs maybe for 161006-64-0

Zhejiang Kangfeng Chemical Co.,LTD.

Contact:+86-579-86709687

Address:Xueshizhai Industrial Zone, Weishan Town,Dongyang City, Zhejiang Province ,China
Beijing Wisdom Chemicals Co., Ltd.

Contact:+86-10-52350335

Address:F2, BLDG 19, Liando Valley U, Majuqiao, Tongzhou District, Beijing, China
Beijing Tianjia Chemical Science & Technology Co.,Ltd

Contact:86-0550-2392698

Address:No.388, Shiliang Road (East),
Beijing Mesochem Technology Co.,LTD

website:http://www.mesochem.com

Contact:0086-10-57862036

Address:2301, Floor 23, Building 9 Lippo Plaza, Yard 8 Ronghua Middle Road, ETDZ, Beijing, China
Shandong Bolode Bio-Technology Co., LTD

Contact:+86-0531-58966870

Address:136 Jingyi Road,Huaiyin District,Jinan,Shandong,China

Relevant to this article

Scaffold hopping identifies 6,8-disubstituted purines as novel anaplastic lymphoma kinase inhibitors

Doi:10.1016/j.ejpb.2017.03.011
(2018)
Rearrangements of Cycloalkenyl Aryl Ethers

Doi:10.3390/molecules21040503
(2016)
Doi:10.1139/v67-311
(1967)
Nucleosides and nucleotides. 151. Conversion of (Z)-2'-(cyanomethylene)-2'-deoxyuridines into their (E)-isomers via addition of thiophenol to the cyanomethylene moiety followed by oxidative syn-elimination reactions

Doi:10.1021/jo960577s
(1996)
The synthesis and Zimmermann reaction of some androsten-16-ones.

Doi:10.1248/cpb.16.126
(1968)
Lipase catalyzed 1,2-addition of thiols to imines under mild conditions

Doi:10.1039/c7nj03387g
(2018)

Article Doi