1987
DOI: 10.1002/chin.198702123
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Synthesis of Cyclic N‐Thioacylamidines from Aminothiocarbonyl Compounds and Activated Lactames.

Abstract: Derivatives of lactames such as amide‐chlorides or lactame‐acetals, are synthesized in situ by the reaction of (I) with POCl3 or with (CH3)2SO4/NaOEt.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2001
2001
2001
2001

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 1 publication
0
1
0
Order By: Relevance
“…[57] When 100 was treated with various alkylating agents like substituted benzyl bromides or chlorides, or phenacyl halogenides, the S-alkyl derivatives 102 were obtained, which underwent ring closure to thiazoles 103. [58] Contrary to the examples described above, the semicyclic aminoacrylonitrile 104 contains an exo double bond activ- Scheme 13 ating position 2. Its reaction with hydrazine follows the general route, and results in formation of the pyrazole compound 105.…”
Section: E Pseudo Ring Transformations (Ring Chain Transformations)mentioning
confidence: 93%
“…[57] When 100 was treated with various alkylating agents like substituted benzyl bromides or chlorides, or phenacyl halogenides, the S-alkyl derivatives 102 were obtained, which underwent ring closure to thiazoles 103. [58] Contrary to the examples described above, the semicyclic aminoacrylonitrile 104 contains an exo double bond activ- Scheme 13 ating position 2. Its reaction with hydrazine follows the general route, and results in formation of the pyrazole compound 105.…”
Section: E Pseudo Ring Transformations (Ring Chain Transformations)mentioning
confidence: 93%