Synthesis of β-hydroxypiperidine alkaloids by anodic oxidation of carbamates and hydroboration

DOI: 10.1139/v96-273

Source and publish data:

Canadian Journal of Chemistry p. 2444 - 2453 (1996)

Update date:2022-09-26

Topics:

Authors:

Plehiers, Mark

Hootelé, Claude

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

Article abstract of DOI:10.1139/v96-273

The β-hydroxypiperidine alkaloids (±)-pseudoconhydrine, (±)-N-methylpseudoconhydrine, (-)-5-hydroxysedamine, and (+)-sedacryptine were synthesized. Successive functionalization of the piperidine ring via anodic methoxylation allowed the regio- and stereos

Full text of DOI:10.1139/v96-273

Products guided by the article

Product name:sedacryptin

Cas No:187456-95-7

R&D Labs maybe for 187456-95-7

NINGBO YINZHOU PRECISE COLOR CO.,LTD.

Contact:86-574-88139809 86-574-83033159

Address:Qiming Road,Yinzhou,Ningbo,China
Nanjing Fubang Chemical Co.,Ltd

Contact:+86-25-83179199

Address:5F,Tianzheng international plaza,No399 Zhongyang Road ,Nanjing China
waho int'l company

Contact:+86-579-85206992

Address:No 451 chouzhou north road ,room 1106 int'l business center , yiwu ,china
Hubei Xiangxi Chemical Industry Co.,Ltd

Contact:+86-710-3454830

Address:No.7, Daqing East Road, Xiangfan City, Hubei Province, China
LIDE PHARMACEUTICALS LIMITED

website:http://www.lidepharma.com

Contact:+86-25-58409506

Address:Chungking Express Nos.36 Nathan Road，Kowloon, HK

Relevant to this article

The tandem Pummerer-isomunchnone route to (±)-pumiliotoxin C

Doi:10.1016/S0040-4039(97)00141-X
(1997)
Investigation of trypanothione reductase inhibitory activity by 1,3,4-thiadiazolium-2-aminide derivatives and molecular docking studies

Doi:10.1016/j.bmc.2012.01.009
(2012)
Doi:10.1021/jo01119a012
(1955)
Synthesis and Characterization of (2,4,6-Trimethylphenylimido)molybdenum Complexes. X-ray Crystal Structures of (L_OEt)Mo(Nmes)₂Cl, (L_OEt)Mo(Nmes)Cl₂, and MoCl₃(Nmes)(depe) (mes = 2,4,6-Trimethylphenyl

Doi:10.1021/ic961190a
(1997)
Antimalarial activity of new dihydroartemisinin derivatives. 7. 4-(p- substituted phenyl)-4(R or S)-[10(α or β)-dihydroartemisininoxy]butyric acids

Doi:10.1021/jm9607919
(1997)
Elimination Reactions of (E)- and (Z)-Benzaldehyde O-Pivaloyloximes. Transition-State Differences for the Syn and Anti Eliminations Forming Nitriles

Doi:10.1021/jo9618637
(1997)

Article Doi