Ring Chain Transformations. XII. Synthesis of N-(3-Aminothioacryloyl)lactam Imines and their Transformation to 4-(ω-Amino-alkyl)thiazoles or N-(Thien-2-yl)lactam Imines

DOI: 10.1002/prac.19933350712

Source and publish data:

Journal fur Praktische Chemie - Chemiker-Zeitung p. 639 - 643 (1993)

Update date:2022-08-17

Topics:

Authors:

Paetzel, Michael

Knoll, Alexander

Steinke, Thomas

Loewis, Michael von

Liebscher, Juergen

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

Article abstract of DOI:10.1002/prac.19933350712

Full text of DOI:10.1002/prac.19933350712

Products guided by the article

Product name:Pyrrolidine, 2,2-dimethoxy-1-methyl-

Cas No:39650-82-3

R&D Labs maybe for 39650-82-3

Chameleon Specialty Chemicals

Contact:+44 7958 511245

Address:PO Box 469, Manchester, UK
Hunan Shineway Enterprise Co., Ltd.

Contact:+86-731-86303875

Address:118, Huanghua International Airport Road, Huanghua Town, Changsha, Hunan 410137, China
Tomo Pharma Chem Co., Limited

Contact:+86-158-05817090

Address:ROOM 9F, FLAT 2, GUODU DEVELOPING BLDG, No.182, ZHAOHUI ROAD
Guangzhou Shiny Co., Ltd.

website:https://www.sinoshiny.com/products

Contact:+86-20-62802632;62802633

Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District
Chengdu Chengnuo New-Tech Co., Ltd

Contact:0086-028-85749078

Address:4 Jiuyang road,Jiulong industrial port,Chengdu, China

Relevant to this article

Pyridine C3-arylation of nicotinic acids accessible via a multicomponent reaction: an entry to all-substituted-3,4-diarylated pyridines

Doi:10.1039/c6ra28299g
(2017)
Synthetic access to the chlorocyclopentane cores of the proposed original and revised structures of palau'amine

Doi:10.1002/anie.200801969
(2008)
Incorporating Energetic Moieties into Four Oxadiazole Ring Systems for the Generation of High-Performance Energetic Materials

Doi:10.1002/cplu.201800107
(2018)
Doi:10.1021/ja00806a037
(1973)
Doi:10.1021/ja00438a044
(1976)
Generation and Oxidative Reactivity of a Ni(II) Superoxo Complex via Ligand-Based Redox Non-Innocence

Doi:10.1021/jacs.0c03244
(2020)

Article Doi