Synthesis of erythrina and related alkaloids. XXII. Intramolecular cyclization approach. (1): New synthetic route to erythrinan and related heterocycles and synthesis of (±)-3-demethoxyerythratidinone

DOI: 10.1248/cpb.38.1462

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1462 - 1472 (1990)

Update date:2022-08-04

Topics:

Authors:

Tsuda Tsuda

Sakai Sakai

Nakai Nakai

Kaneko Kaneko

Ishiguro

Isobe Isobe

Taga Taga

Sano Sano

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

Article abstract of DOI:10.1248/cpb.38.1462

Full text of DOI:10.1248/cpb.38.1462

NII-Electronic Library Service

Products guided by the article

Product name:2-[2-(3,4-Dimethoxy-phenyl)-ethylamino]-cyclopent-1-enecarboxylic acid ethyl ester

Cas No:130655-36-6

R&D Labs maybe for 130655-36-6

Li's chemicals

Contact:+86-15850770348

Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China
NOVASYNCS CO., LTD

Contact:0512-63006287

Address:no.88.YISHENG Road,etdz-WUJIANG,SUZHOU,CHINA
miao tie sheng

Contact:0311-13263231263

Address:jian hua street,Shijiazhuang City, China
SPE Chemicals Co.,Ltd

Contact:

Address:ROOM 1715, No#345 Jin Xiang Road, Pudong District
Chengdu Green Young Biopharmaceutical INC

Contact:+86-28-85337952

Address:1-B-26,Tianhe Industry Park, No.1480 of Tianfu Road,Chengdu,P.R.China,610000

Relevant to this article

Physicochemical studies of molecular hyperpolarizability of imidazole derivatives

Doi:10.1016/j.saa.2011.02.024
(2011)
Rescuing biological activity from synthetic phakellistatin 19

Doi:10.1021/jm401520x
(2013)
The Synthesis of Some Ethers and Mixed Ether Esters of Glycerol

Doi:10.1071/CH9901445
(1990)
Gold-catalyzed alkylation of silyl enol ethers with ortho-alkynylbenzoic acid esters

Doi:10.3762/bjoc.7.76
(2011)
Novel PDC catalyzed oxidative rearrangement of tertiary allylic alcohols to β-substituted enones

Doi:10.1016/j.tetlet.2015.09.046
(2015)
Damage of aromatic amino acids by the atmospheric free radical oxidant NO₃ in the presence of NO₂, N₂O₄, O₃ and O₂

Doi:10.1039/c0ob01186j
(2011)

Article Doi