CORYPALLINE AND O-METHYLCORYPALLINE, TWO ALKALOIDS FROM PAPAVER BRACTEATUM

DOI: 10.1016/S0031-9422(00)80099-0

Source and publish data:

Phytochemistry p. 247 - 250 (1983)

Update date:2022-08-04

Topics:

Authors:

Theuns, Hubert G.

Vlietstra, Edward J.

Salemink, Cornelis A.

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

Article abstract of DOI:10.1016/S0031-9422(00)80099-0

Two new Papaver alkaloids, corypalline and O-methylcorypalline, were identified from P. bracteatum.These alkaloids are considered as the biosynthetic precursors of N-methylcorydaldine in this plant.Key Word Index - Papaver bracteatum; Papaveraceae; alkaloids; tetrahydroisoquinolines; corypalline; O-methylcorypalline; biosynthetic pathway; 8-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline-7-ol; synthesis.

Full text of DOI:10.1016/S0031-9422(00)80099-0

Products guided by the article

Product name:N-(3-benzyloxy-2-hydroxybenzyl) N-methylaminoacetaldehyde dimethyl acetal

Cas No:87339-93-3

R&D Labs maybe for 87339-93-3

Shanggao Ruiya Fine Chemicals Co., Ltd

Contact:+86-795-2592103

Address:Xingguang Nanlu,Shanggao County Industry Park
Golden Union Agrochemical Import and Export Co., Ltd.

Contact:86-755-23910527

Address:Room 1106, Tower 3A, Excellence Century Center, Futian District, Shenzhen, China
Jiangsu Willing Bio-Tech Co ltd

website:http://www.willingbio.com/

Contact:+86 18796908173

Address:No 18 Guoqiao Road
Hangzhou Sartort Biopharma Co., Ltd

website:http://www.sartort.com

Contact:86-571-87039693

Address:No. 57, Tech Park Road, Hangzhou, Zhejiang, China
Hubei anhuang chemical Co.Ltd

Contact:

Address:308# dongwu avenue dongxihu district wuhan city

Relevant to this article

Ruthenium mediated C-H activation of 2-(arylazo)phenols: Characterization of an intermediate and the final organoruthenium complex

Doi:10.1021/ic051874v
(2006)
Catalytic hydrocyanation of olefins by nickel(0) phosphite complexes - Effects of Lewis acids

Doi:10.1021/om00079a008
(1984)
N^ω-alkylnitrosocarbamoyl-α,ω-diaminogarboxy lic acids. 3. Synthesis and antitumor activity of N^ε-nitroso-N ^ε-[N′-(2-chloroethyl)carbamoyl]-L-lysine and N ^ε-[N′-(2-chloroethyl)-N′-nitroso-carbamoyl]-L-lysine

Doi:10.1007/BF02333967
(1996)
Conversion of Aromatic Ketones into α-Arylalkanoic Acids. Part 2. Routes Employing Peracid, Chlorine, or Nitrous Acid

Doi:10.1039/P19830001483
(1983)
Synthesis of vinylic sulfones in aqueous media

Doi:10.1021/acs.orglett.0c04257
(2021)
SYSTEMATIC SYNTHESIS OF PURINE 8,5'-IMINO AND SUBSTITUTED IMINO CYCLONUCLEOSIDES

Doi:10.1246/cl.1983.1017
(1983)

Article Doi