Scholarly article on Carbon-13C dioxide 1111-72-4 from Transactions of the Faraday Society p. 2598 - 2606

DOI: 10.1039/TF9716702598

Source and publish data:

Transactions of the Faraday Society p. 2598 - 2606 (1971)

Update date:2022-08-11

Topics:

Authors:

Dominey, D. A.

Wickham, A. J.

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

Article abstract of DOI:10.1039/TF9716702598

Full text of DOI:10.1039/TF9716702598

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:Carbon-13C dioxide

Cas No:1111-72-4

R&D Labs maybe for 1111-72-4

BIOS CHEMICALS

Contact:+33-5-34012600

Address:28 ZA des Pignès
Linyi VIHO Chemical Co.,Ltd

Contact:86-15588110016

Address:LINYI CITY,SHANDONG PROVINCE,CHINA
Nanjing Habo Medical Technology Co., Ltd.

Contact:025－85769882

Address:No.108. Ganjiabian east. Qixia District .Nanjing
Shanghai better-in Medical Technology Co.,LTD.

Contact:+86-21-38921049

Address:Lane 720 zhangjianggaoke cailun road, Pudong, Shanghai, room 513
Changzhou Welton Chemical Co., Ltd,

Contact:0086-519-85910828,85920537,85912897

Address:No.8 Jinlong Road, Binjiang Park, Changzhou, Jiangsu, China.

Relevant to this article

Practical one-pot synthesis of 5-alkynyl-1,2,3-triazoles via heterogeneous copper(I)-catalyzed tandem three-component click/alkynylation reaction

Doi:10.1002/aoc.5319
(2020)
Acidic 1,3-propanediaminetetraacetato lanthanides with luminescent and catalytic ester hydrolysis properties

Doi:10.1016/j.jssc.2014.07.037
(2014)
Efficient conversion of alkenes to chlorohydrins by a Ru-based artificial enzyme

Doi:10.1039/c6cc08873b
(2017)
Organocatalytic asymmetric friedel-crafts alkylation of indoles with simple α,β-unsaturated ketones

Doi:10.1021/ol070309o
(2007)
Optical resolution of baclofen via diastereomeric salt pair formation between 3-(p-chlorophenyl)glutaramic acid and (S)-(-)-α-phenylethylamine

Doi:10.1039/a606037d
(1997)
Ni₂P hollow microspheres for electrocatalytic oxygen evolution and reduction reactions

Doi:10.1039/c8cy00211h
(2018)

Article Doi

DOI: 10.1039/TF9716702598