A convenient synthetic approach to new α-(9-fluorenylmethoxycarbonylamino)alkylphosphonic acid derivatives

DOI: 10.1055/s-1992-26344

Source and publish data:

Synthesis p. 1226 - 1228 (1992)

Update date:2022-08-03

Topics:

Authors:

Dumy Dumy

Escale Escale

Girard Girard

Parello Parello

Vidal Vidal

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

Article abstract of DOI:10.1055/s-1992-26344

Benzyl hydrogen α-(9-fluorenylmethoxycarbonylamino)alkylphosphonates 4, obtained by the sodium metaperiodate oxidation of the corresponding phosphinates 3, were converted to the chloridates 5 and coupled with the N(ε)-protected lysine benzyl ester to affo

Full text of DOI:10.1055/s-1992-26344

Products guided by the article

Product name:benzyl α-(9-fluorenylmethoxycarbonylamino)methylphosphinate

Cas No:146406-33-9

R&D Labs maybe for 146406-33-9

Chongqing KonAo Health Co.,Ltd

Contact:13687578375

Address:wuhan hubei china
Chengdu Pukang Biotechnology Co., Ltd

Contact:+86-28-82550498

Address:No. 558 Rulin Road,Xinjin county,Chengdu city, China
Jinan Great Chemical Co.,Ltd.

Contact:+86-531-58668191 58668193 58668196 58661173

Address:No 55,Beixiaoxinzhuang West Street,Jinan City, Shandong Province
Zhaodu Fine Chemical Plant

Contact:86-310-8067016

Address:East Fuhua Road,Tiexi Chemical Industrial Estate,Hebei,China
ChangZhou XiaQing Chemical Co., Ltd.

Contact:+86-519-88721665

Address:3# Hengluo Road, Henglin Town, Changzhou City, Jiangsu Province，China

Relevant to this article

Differential O-3/O-4 selectivity in the glycosylation of N-dimethylmaleoyl-protected hexosamine acceptors: Effect of a conformationally armed (superarmed) glycosyl donor

Doi:10.1016/j.carres.2013.08.002
(2013)
N-Heterocyclic carbene-palladium(ii)-1-methylimidazole complex catalyzed direct C-H bond arylation of imidazo[1,2-a]pyridines with aryl chlorides

Doi:10.1039/C6OB02704K
(2017)
Ruthenium(II) carbonyl complexes bearing quinoline-based NNO tridentate ligands as catalyst for one-pot conversion of aldehydes to amides and o-allylation of phenols

Doi:10.1016/j.saa.2013.07.114
(2013)
Active Site-Directed Synthetic Thrombin Inhibitors: Synthesis, in Vitro and in Vivo Activity Profile of BMY 44621 and Analogs. An Examination of the Role of the Amino Group in the D-Phe-Pro-Arg-H Series

Doi:10.1021/jm00054a018
(1993)
Discovery of 5-(2′,4′-difluorophenyl)-salicylanilides as new inhibitors of receptor activator of NF-κ°B ligand (RANKL)-induced osteoclastogenesis

Doi:10.1016/j.ejmech.2015.05.015
(2015)
1,4-Diacyl-3-acylamino-5-aryl-4,5-dihydro-1H-1,2,4-triazoles: Ring Closure Products of Aromatic Carbaldehyde (Diaminomethylene) Hydrazones with Acylating Agents

Doi:10.1007/BF00807164
(1995)

Article Doi