NMR spectra of organogermanium compounds. X.1) Syntheses, 13C and 73Ge NMR spectra and molecular mechanics calculations of germacyclopentanes and germacyclopentenes

DOI: 10.1246/bcsj.64.91

Source and publish data:

Bulletin of the Chemical Society of Japan p. 91 - 98 (1991)

Update date:2022-09-26

Topics:

Authors:

Takeuchi

Tanaka Tanaka

Harazono

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

Article abstract of DOI:10.1246/bcsj.64.91

Full text of DOI:10.1246/bcsj.64.91

Products guided by the article

Product name:1,1-Diethyl-3-methylgermacyclopenta-3-ene

Cas No:5764-76-1

R&D Labs maybe for 5764-76-1

Melone Pharmaceutical Co., ltd

Contact:+86-411 82593920, 82593631

Address:No 232, JInma Roda, Development Zone, Dalian, China
Qingdao Pana-Life Biochem Co.,Ltd.

Contact:86-532-87683902

Address:No.967 Dalao Road, Licang Zone, Qingdao City,Shandong, China 266021
Zibo Xiaoguang Chemical Material Co., Ltd

Contact:15954099116

Address:Boshan Development Zone
Shanghai Demand Chemical Co., ltd，China

Contact:86-021-55237578/55239122

Address:Room 3H, No.578, Yingkou Road, Yangpu District, Shanghai, China
Jewim Pharmaceutical (Shandong) Co., Ltd

Contact:+8615621883869

Address:山东省泰安市高新技术产业开发区配天门大街西首

Relevant to this article

Polydiacetylenes Containing 2-Picolylamide Chemosensor for Colorimetric Detection of Cadmium Ions

Doi:10.1002/bkcs.12163
(2021)
Doi:10.1016/S0040-4039(00)75042-8
(1975)
Ethoxymethylenemalonates and Malononitriles (EMM reagents) as formic acid equivalents: Synthesis of fused-imidazoles under neutral or mildly acidic con

Doi:10.1016/S0040-4039(00)91957-9
(1993)
Stereochemistry of baker's yeast mediated reduction of α,β-unsaturated δ-lactones in the goniothalamin series

Doi:10.1016/0957-4166(94)80139-8
(1994)
Gold glyconanoparticles: Synthetic polyvalent ligands mimicking glycocalyx-like surfaces as tools for glycobiological studies

Doi:10.1002/chem.200204544
(2003)
Design, Synthesis, and Structure-Activity Relationship of New Pyrimidinamine Derivatives Containing an Aryloxy Pyridine Moiety

Doi:10.1021/acs.jafc.6b05580
(2017)

Article Doi