Bonding in Phenylhydrazones: X-Ray Crystal Structure and Theoretical Calculations Involving (E)-Acetophenone Phenylhydrazone

DOI: 10.1007/BF00817313

Source and publish data:

Monatshefte fur Chemie p. 775 - 782 (1993)

Update date:2022-08-16

Topics:

Authors:

Porter, L. C.

Ming-Li Ming-Li

Cervantes-Lee, F.

Murray III, H. H.

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

Article abstract of DOI:10.1007/BF00817313

Semiempirical (PM3 type) calculations have been carried out on the E isomer of acetophenone phenylhydrazone and extended to include acetophenoneimine and phenylhydrazone.The optimized structure of acetophenone phenylhydrazone ha also been compared with th

Full text of DOI:10.1007/BF00817313

Products guided by the article

Product name:Ethanone, 1-phenyl-, phenylhydrazone, (1E)-

Cas No:59130-82-4

R&D Labs maybe for 59130-82-4

Shanghai Sungo Technology Chemical Co., Ltd

Contact:0086-21-51385579

Address:Room2010, F/20, Tonghua Plaza, NO 345 Jinxiang Road, Jinqiao Export Processing Zone, Shanghai, 201206 P.R.CHINA
Zipont chem(wuhan）Tech co.，Ltd

Contact:+86-27-87587198

Address:wuhan
HUNAN CHEMAPI BIOLOGICAL TECHNOLOGY CO.,LTD.

Contact:+86-186-02659358

Address:1004, building 3, Wanke Jinsemaitianyuan, 498 Guitang Road, Yuhua District, Changsha City, Hunan Province, China
Shaanxi Lighte Optoelectronics Material Co., Ltd.

Contact:+86-29-88320728-622/619/620

Address:No.55 INDUSTRY ROAD 2,XI'AN NATIONAL CIVIL AEROSPACE INDUSTRIAL PARK.XI'AN China 710065.
shanghai hekang chemical co.ltd

Contact:021-54173790

Address:328 WuHe Road, Building #A, 2nd Floor, Minhang, Shanghai 201109, China

Relevant to this article

Diisobutylaluminum borohydride: An efficient reagent for the reduction of tertiary amides to the corresponding amines under ambient conditions

Doi:10.1016/j.tetlet.2017.09.030
(2017)
Dynamic Transformation between Covalent Organic Frameworks and Discrete Organic Cages

Doi:10.1021/jacs.0c11073
(2020)
Cu(ii) complex heterogenized on SBA-15: A highly efficient and additive-free solid catalyst for the homocoupling of alkynes

Doi:10.1039/c3ra44213f
(2014)
First asymmetric synthesis of a 6-alkoxy-5,6-dihydro-1,3-oxazine: A promising enantioselective route to β-amido aldehydes

Doi:10.1021/ol991326j
(2000)
Electrochemical radical reactions of alkyl iodides: a highly efficient, clean, green alternative to tin reagents

Doi:10.1039/d0sc01694b
(2020)
Metal-Free Synthesis of Fully Substituted Pyridines via Ring Construction Based on the Domino Reactions of Enaminones and Aldehydes

Doi:10.1021/acs.joc.6b01149
(2016)

Article Doi