Observation of a Nonconcerted Double Proton Transfer in Solid State by 15N CPMAS NMR

DOI: 10.1021/ja00237a065

Source and publish data:

Journal of the American Chemical Society p. 929 - 930 (1987)

Update date:2022-08-10

Topics:

Authors:

Limbach, H. H.

Wehrle, B.

Zimmermann, H.

Kendrick, R. D.

Yannoni, C. S.

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

Article abstract of DOI:10.1021/ja00237a065

Full text of DOI:10.1021/ja00237a065

Products guided by the article

Product name:1,2-Benzenediamine-15N2

Cas No:116006-97-4

R&D Labs maybe for 116006-97-4

NanJing KaiHeng Chemical CO., LTD.

Contact:+86-25-85768391

Address:RM.1704, D, WANDA PLAZA, NO.110, MIDDLE JIANGDONG ROAD, NANJING, CHINA
Shanghai Egoal Chemical Co.,Ltd

Contact:+86-21-50333091

Address:Yangming Garden Square 3,YangGao North Road 1188, Pudong New District, Shanghai
ZK Biochem Group Co., Ltd

Contact:+86-532-80762375

Address:No. 6, Hongkong Middle Road, Qingdao, China
Chinese Peptide Company

Contact:86-571-86737118-8689

Address:No.69, 12 Street, HEDA, Hangzhou, Zhejiang, China
Shandong Wanda Organosilicon New Material Co., Ltd

Contact:+86-21-54177116;54302881

Address:R1318 Greenland No. 3 Lane 58 Xinjian East Rd., Minhang

Relevant to this article

Mechanistic studies of the azomethine ylide-forming photoreactions of N- (silylmethyl)phthalimides and N-phthaloylglycine

Doi:10.1021/ja9841862
(1999)
Stepwise synthesis and characterization of germa[4], [5], [8], and [10]pericyclynes

Doi:10.1039/c5dt01411e
(2015)
A dynamic kinetic asymmetric transfer hydrogenation-cyclization tandem reaction: An easy access to chiral 3,4-dihydro-2: H -pyran-carbonitriles

Doi:10.1039/c7cc02156a
(2017)
Asymmetric aldol reaction of 3-acetyl-2H-chromen-2-ones and isatins catalyzed by a bifunctional quinidine urea catalyst

Doi:10.1002/adsc.201300623
(2014)
Borontrifluoride etherate promoted one-pot conversion of nitriles to esters

Doi:10.1081/SCC-120024013
(2003)
Enhancement of the electrical stability of ZnO varistors by a novel immersion process

Doi:10.1111/j.1551-2916.2011.04453.x
(2011)

Article Doi