Stereochemical course in tungsten-promoted cyclocarbonylation reactions to form five-, six-, and seven-membered lactone rings

DOI: 10.1021/ja00115a031

Source and publish data:

Journal of the American Chemical Society p. 2933 - 2934 (1995)

Update date:2022-08-03

Topics:

Authors:

Chen, Chi-Chung

Fan, Jang-Shyang

Lee, Gene-Hsian

Peng, Shie-Ming

Wang, Sue-Lang

Liu, Rai-Shung

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

Article abstract of DOI:10.1021/ja00115a031

Full text of DOI:10.1021/ja00115a031

Products guided by the article

Product name:(C₅H₅)W(CO)3CH₂CCCH₂CH(OH)(C₆H₅)

Cas No:163491-08-5

R&D Labs maybe for 163491-08-5

Wuhan Benjamin Pharmaceutical Chemical Co.,Ltd

Contact:86-27-52341789

Address:Room 1518 B suite, optical valley time square, No 111 Guanshan Road, Hongshan District,Wuhan,Hubei Province,China.
SYN Pharma Co., Ltd

Contact:86-21 60347964

Address:No.1304, West Meilong Road, Minhang District, Shanghai, China
Zhenjiang Haitong Chemical Industry Co., Ltd.

Contact:+86 (511) 8448-0369

Address:Baoyan Town, Dantu District, Zhenjiang City, Jiangsu, China
zhuzhou zhongle chemical co. ltd.

Contact:+86-0731 28228409

Address:Zhuzhou, Hunan, China
xuri chemicals co., ltd

Contact:86-516-66656369

Address:The west road of Huaihai, Xuzhou, China

Relevant to this article

New and convenient syntheses of anhydro-2-alkyl-3-iminothiazolo[3,2-a]pyridinium hydroxide derivatives

Doi:10.1016/S0040-4039(97)00415-2
(1997)
Two mono- and dinuclear Ni(II) complexes constructed from quinazoline-type ligands: Synthesis, X-ray structures, spectroscopic, electrochemical, thermal, and antimicrobial studies

Doi:10.1016/j.poly.2017.04.010
(2017)
Asymmetric Total Synthesis of Bioactive Natural Lipid Mycalol

Doi:10.1021/acs.joc.5b00972
(2015)
Synthesis of carbodiimides by I₂/CHP-mediated cross-coupling reaction of isocyanides with amines under metal-free conditions

Doi:10.1021/acs.orglett.5b00722
(2015)
Facile synthesis of enol ethers via Zn(OTf)₂-mediated formal alkyne hydration-Smiles rearrangement

Doi:10.1039/c4ra00159a
(2014)
Doi:10.1021/ja01291a008
(1937)

Article Doi