ENANTIOSELECTIVE SYNTHESIS OF (+)-CITREOVIRAL USING ASYMMETRIC HYDROXYLATION OF TIGLATE ESTERS

DOI: 10.1016/S0040-4039(00)99033-6

Source and publish data:

Tetrahedron Letters p. 6485 - 6488 (1985)

Update date:2022-07-30

Topics:

Authors:

Hatakeyama, Susumi

Matsui, Yumiko

Suzuki, Masahiro

Sakurai, Kuniya

Takano, Seiichi

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

Article abstract of DOI:10.1016/S0040-4039(00)99033-6

A microbial metabolite (+)-citreoviral has been synthesized enantio- and stereo-selectively using newly developed asymmetric hydroxylation of tiglate esters for the construction of the key chiral building block.

Full text of DOI:10.1016/S0040-4039(00)99033-6

Products guided by the article

Product name:(1R,2S,3R,4S)-3-(2,2-dimethylpropoxy)-1,7,7-trimethylbicyclo<2.2.1>heptan-2-ol

Cas No:85695-92-7

R&D Labs maybe for 85695-92-7

Xiamen Goodhealth Pharmchem Co., Ltd.

Contact:0086-592-2097683

Address:404R No.2 54# Minzu Rd., Xiamen, China
wuxi huabin bio-tech Co.,Ltd(expird)

Contact:86-0510-85133006

Address:hubin road NO157
Puyang Huicheng Electronic Material Co., Ltd

website:http://huichengchem.weba.testwebsite.cn/index_en.html

Contact:+86-393-8910800

Address:West Section Shengli Road, Puyang457000, China
SHAANXI TOP PHARM CHEMICAL CO.LTD

Contact:+86-029-85733403

Address:No.108 ,west sector,south er huan,xi'an,china
shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China

Relevant to this article

Doi:10.1021/ja01146a526
(1951)
Effect of o-methyl group on rate, mechanism, and resonance contribution: Aminolysis of Y-substituted phenyl X-substituted 2-methylbenzoates

Doi:10.1021/jo050172k
(2005)
Doi:10.1021/ja01193a048
(1947)
Some imines and azo compounds containing furoxan ring synthesized from methylisoeugenol

Doi:10.1002/jhet.5570430635
(2006)
Doi:10.1021/jo00832a074
(1970)
Doi:10.1021/jo01194a007
()

Article Doi