Scholarly article on (C6H5)3P(C5H4)W(CO)3BF3 32238-39-4 from Journal of Organometallic Chemistry p. 425,434,435

DOI: 10.1016/S0022-328X(00)86063-5

Source and publish data:

Journal of Organometallic Chemistry p. 425,434,435 (1970)

Update date:2022-08-05

Topics:

Authors:

Kotz Kotz

Pedrotty

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

Article abstract of DOI:10.1016/S0022-328X(00)86063-5

Full text of DOI:10.1016/S0022-328X(00)86063-5

Products guided by the article

Product name:(C₆H₅)3P(C₅H₄)W(CO)3BF₃

Cas No:32238-39-4

R&D Labs maybe for 32238-39-4

shanghai payne pharm co.,ltd.

Contact:+86-021-58123769

Address:No.780 of Cailun Road,Zhangjiang Hi-tech Park,Pudong,Shanghai
Chengdu Pukang Biotechnology Co., Ltd

Contact:+86-28-82550498

Address:No. 558 Rulin Road,Xinjin county,Chengdu city, China
NINGBO YINLIANG FOREIGN TRADE CO., LTD.

Contact:+86-574-87834016 / 87898057

Address:23F NO.666JINYU ROAD,YINGZHOU DISTRICT,NINGBO.CHINA
Weihao Chemtech (ChangZhou) Co., Ltd.(expird)

Contact:051989185693

Address:NO 217 huangshan Rd ,Changzhou
Lanling Hongchuang Flame Retardant Co., Ltd.

Contact:+86-531-68858132

Address:East Huafeichang Road, Cangshan County, Linyi, Shandong, China (Mainland)

Relevant to this article

N-substituted 2-amino-4-pentenoic acids for amino acid protection and resolution

Doi:10.1016/S0040-4020(00)00826-7
(2000)
Doi:10.1007/BF00909335
(1971)
Zn(OAc)₂·2H₂O-catalyzed one-pot efficient synthesis of α-amino nitriles

Doi:10.14233/ajchem.2014.17180
(2014)
Synthesis, spectroscopic and physicochemical investigations of environmentally benign heterocyclic Schiff base derivatives as antibacterial agents on the bases of in vitro and density functional theory

Doi:10.1016/j.jphotobiol.2013.01.007
(2013)
Indium trichloride catalyzed one-pot synthesis of indolo[2,1-a]pyrrolo[4′,3′:2,3]-7a,8,13,13b-tetrahydroquinolines through intramolecular imino Diels-Alder reactions

Doi:10.1016/j.tetlet.2007.03.170
(2007)
Lewis acid promoted anomerisation of alkyl O- and S-xylo-, arabino- and fucopyranosides

Doi:10.1016/j.carres.2018.11.010
(2019)

Article Doi

DOI: 10.1016/S0022-328X(00)86063-5