The synthesis of lupin alkaloids. II. A formal synthesis of (±)-sparteine

DOI: 10.1248/cpb.35.4990

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 4990 - 4992,4990-4992 (1987)

Update date:2022-07-29

Topics:

Authors:

Takatsu Takatsu

Noguchi Noguchi

Ohmiya Ohmiya

Otomasu Otomasu

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

Article abstract of DOI:10.1248/cpb.35.4990

Full text of DOI:10.1248/cpb.35.4990

Products guided by the article

Product name:8-oxosparteine

Cas No:36454-89-4

R&D Labs maybe for 36454-89-4

Jiangsu Zenji Pharmaceuticals LTD

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

Address:No.5 Xinmofan Road
NanJing KaiHeng Chemical CO., LTD.

Contact:+86-25-85768391

Address:RM.1704, D, WANDA PLAZA, NO.110, MIDDLE JIANGDONG ROAD, NANJING, CHINA
SHANDONG CREDAGRI CHEMICAL CO., LTD.

Contact:+86-531-88872050

Address:ROOM 601A, BUILDING 2, SHUNTAI SQUARE, NO. 2000 SHUNHUA ROAD, HI-TECH DEVELOPMENT ZONE, JINAN, CHINA.
Shanghai Synmedia Chemical Co., Ltd

Contact:+86-21-38681880

Address:6th Floor, 11A Building, No.528 Ruiqing Road, Heqing town, Pudong new district, Shanghai China
Shanghai Zhihua ChemTech Co., Ltd.

Contact:+86-13774313779

Address:Room 817 Suite B 3333 Shenjiang Road

Relevant to this article

Synthesis of dipeptide-bound epoxides and α,β-unsaturated amides as potential irreversible transglutaminase inhibitors

Doi:10.1016/S0968-0896(01)00292-9
(2002)
Characterization of New Methyl-Substituted Tetralins and Indans by 13C NMR Spectroscopy

Doi:10.1002/mrc.1260330706
(1995)
Doi:10.1021/jm00253a016
(1974)
Synthesis, characterization crystal structures and DNA binding studies of zinc complexes with oxygen and nitrogen donor ligands

Doi:10.1016/j.poly.2019.114273
(2020)
Photogenerated Radical in Phenylglyoxylic Acid for in Vivo Hyperpolarized 13C MR with Photosensitive Metabolic Substrates

Doi:10.1021/jacs.8b09326
(2018)
Synthesis of tubuphenylalanine and epi-tubuphenylalanine via regioselective aziridine ring opening with carbon nucleophiles followed by hydroboration-oxidation of 1,1-substituted amino alkenes

Doi:10.1016/j.tet.2018.10.024
(2018)

Article Doi