Fluorodiazadiphosphetidines, XIII: The Reaction of 2,2,2,4,4,4-Hexafluoro-1,3-dimethyl-1,3,2λ5,4λ5-diazadiphosphetidines with Alcohols

DOI: 10.1007/BF00798756

Source and publish data:

Monatshefte fur Chemie p. 881 - 898 (1984)

Update date:2022-08-04

Topics: Alcohols Reaction Experimental

Authors:

Hahn, Heinrich

Toifl, Erich

Meindl, Wolfgang

Utvary, Kurt

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

Article abstract of DOI:10.1007/BF00798756

Nucleophilic substitution reactions of (CH3NPF3)2 with alcohols have been studied.In case of (CH3NPF3)2 as starting material an excess of this compound acts as an HF-acceptor.In this way mono- or di-alkoxysubstituted diazaphosphetidines are obtained.If the starting material is a substituted ring or if an aromatic alcohol is employed, the alcohol component has to be in form of the lithium salt. - Keywords: Aza; Cyclic (non-carbon); Heterocyclic (N,P); Phospha; Alcohol

Full text of DOI:10.1007/BF00798756

Products guided by the article

Product name:2,2,4,4-Tetrafluoro-1,3-dimethyl-2,4-bis-(2-methyl-cyclohexyloxy)-2λ⁵,4λ⁵-[1,3,2,4]diazadiphosphetidine

Cas No:94445-91-7

R&D Labs maybe for 94445-91-7

Shanghai Rainbow Chemistry Co., Ltd.

Contact:+86-21-64968086-5815/5812

Address:3rd floor, Building 7, 251 Faladi Road, Zhangjiang Hi-Tech Park, Pudong District, Shanghai, P.R. China
MS( MAOSHENG )Chemical CO.,LTD

Contact:+86-519-82726678.82726378

Address:TAOXI INDUSTRY ZONE JINTAN
Hunan Zhongqi Pharmaceutical Co., Ltd

website:http://www.hnzqzy.com

Contact:0730-8722288 13807308622

Address:Wanjiafan Road ,Yueyang Economic And Technological Development Zone ,Hunan,PRC
Guarson Chemical Co., Ltd.

website:http://www.guarson.com

Contact:+86-523-88059600,+86-13805268803

Address:Room B1006,Yafang Building,Jiangyan Avenue,Jiangyan District, Taizhou City,Jiangsu,China
Shanghai Hanshare Industry Co.,Ltd.

Contact:86 21 20960688

Address:RM902-903,Building E, Wanda Plaza,No.26,Zhoukang Road, Pudong District, Shanghai, China

Relevant to this article

Stereoselective synthesis of oxazino[4,3-a]indoles employing the oxa-Pictet-Spengler reaction of indoles bearing N-tethered vinylogous carbonate

Doi:10.1039/c0cc05558a
(2011)
Synthesis of 3-indole derivatives by copper sulfonato Salen catalyzed three-component reactions in water

Doi:10.1039/c0cc05695b
(2011)
Selective activation of enantiotopic C(sp³)-hydrogen by means of chiral phosphoric acid: Asymmetric synthesis of tetrahydroquinoline derivatives

Doi:10.1021/ja2014955
(2011)
EIN EINFACHER WEG ZU DERIVATEN DES α-TRIFLUORMETHYLSUBSTITUIERTEN PHENYLALANINS VIA 4-BENZYL-4-TRIFLUORMETHYL-5(4H)-OXAZOLONE

Doi:10.1016/S0022-1139(00)80450-9
(1990)
CYCLOADDITION DIPOLAIRE 1,3 DES 4-ARYLIDENE OXAZOL-5-ONES AVEC LA DIPHENYLNITRILIMINE

Doi:10.1016/S0040-4039(00)88860-7
(1990)
Synthesis of (ε-¹³C-,ε-¹⁵N)-enriched L-lysine - Establishing schemes for the preparation of all possible ¹³C and ¹⁵N isotopomers of L-lysine, L-ornithine, and L-proline

Doi:10.1002/ejoc.200400370
(2004)

Article Doi