Alkaloids from Streptomyces sp. NA-337

DOI: 10.1248/cpb.22.2916

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2916 - 2920 (1974)

Update date:2022-08-04

Topics:

Authors:

Onda Onda

Konda Konda

Narimatsu

Tanaka Tanaka

Awaya Awaya

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

Article abstract of DOI:10.1248/cpb.22.2916

Full text of DOI:10.1248/cpb.22.2916

NII-Electronic Library Service

Products guided by the article

Product name:Pyrrolidine, 4-methyl-2-pentyl- (9CI)

Cas No:769061-69-0

R&D Labs maybe for 769061-69-0

Shanghai Massive Chemical Technology Co., Ltd.

website:http://www.massivechem.com/

Contact:+86 21 34943721

Address:Room 435, 4th floor, Building 9, No. 2568 Gudai Road,Minhang District, Shanghai,
ZK Biochem Group Co., Ltd

Contact:+86-532-80762375

Address:No. 6, Hongkong Middle Road, Qingdao, China
Changzhou LanXu Chemical Co.,ltd.(expird)

Contact:86-0519-86330911,13656129734,15261186386

Address:Room 524, Depart.Chemical, Changzhou Science and Eductaion town, Jiangsu, China;Factory: Haian Fine Chemical Industry Park,Nantong,Jiangsu,China
taicang liyuan chemical co,.ltd

website:http://www.tcliyuanchem.com/productse.php

Contact:86-512-53539583

Address:Room 804,Huaxu Building,No.95,Renmin South Road,Taicang city,Jiangsu Province,China
Jiangsu Zenji Pharmaceuticals LTD

Contact:+86-025-83172562; +1-224-888-1133(USA)

Address:No.5 Xinmofan Road

Relevant to this article

COPPER INDUCED SOLVOLYSIS OF SULFUR COMPOUNDS

Doi:10.1016/S0040-4039(00)99932-5
(1984)
Asymmetric synthesis of α-amino 1,3-dithioketals from sulfinimines (N-sulfinyl imines). Synthesis of (2S,3R)-(-)-3-hydroxy-3-methylproline

Doi:10.1021/ol0485971
(2004)
Studies on the total synthesis of rifamycin. A method for the closure of the macrocyclic unit

Doi:10.1016/S0040-4039(00)71481-X
(1980)
Telluraxanthene

Doi:10.1007/BF00496600
(1980)
Annulations of 5-Phenylthiobutenolides and First Synthesis of (±)-Indanostatin

Doi:10.1055/s-0037-1611462
(2019)
Phosphohomocysteine Derivatives

Doi:10.1055/s-1980-29312
(1980)

Article Doi