Synthetic studies on Lythraceae alkaloids. I. A convenient synthesis of isopelletierine (Japanese)

DOI: 10.1248/yakushi1947.94.4_531

Source and publish data:

Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan p. 531 - 532 (1974)

Update date:2022-08-29

Topics:

Authors:

Hanaoka Hanaoka

Ogawa Ogawa

Arata Arata

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

Article abstract of DOI:10.1248/yakushi1947.94.4_531

Full text of DOI:10.1248/yakushi1947.94.4_531

NII-Electronic Library Service

Products guided by the article

Product name:pelletierine

Cas No:4396-01-4

R&D Labs maybe for 4396-01-4

Shanghai ZaiQi Bio-Tech Co., Ltd.,

Contact:+86-21-5482 4098

Address:Bldg. No.7, No.201 MinYi Rd，Songjiang CaoHeJing High-Tech Park Shanghai 201516 P,R,China
Sichuan JieYao Co., Ltd.

Contact:+86-838-5655598

Address:Guanghan Nanfeng Industrial Zone
Zhejiang Chemline International Co., Ltd.

Contact:+86-571-88062298

Address:Hengdian Industry Area, Dongyang, Zhejiang, China
Changsha Botaniex Inc.

Contact:(86) 731 88718666

Address:Room 1222, Unit 4, Building B, Shangcheng, No.47, Kaiyuan East Road.
uni source industries limited

Contact:86 21 3772 9386

Address:Rm.1803,Starry Bldg.1,1505 Meijiabang Road,Shanghai 201620 China

Relevant to this article

Conjugated dyes carrying N, N-dialkylamino and ketone groups: One-component visible light Norrish type II photoinitiators

Doi:10.1016/j.dyepig.2016.10.034
(2017)
A cellulose-supported Mn(salen)Cl complex as an efficient heterogeneous catalyst for the selective oxidation of benzylic alcohols

Doi:10.1007/s13738-014-0457-z
(2015)
Doi:10.1021/ja01370a057
(1930)
Doi:10.1007/BF00850990
()
An analysis of the bonding properties of benz[a]azulene by X-ray, NMR, and computational studies

Doi:10.1002/hlca.19960790326
(1996)
Stereospecific biocatalytic epoxidation: The first example of direct regeneration of a FAD-dependent monooxygenase for catalysis

Doi:10.1021/ja034119u
(2003)

Article Doi