1992
DOI: 10.1002/chin.199212192
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: A Novel Dieckmann‐Type Cyclization, the Final Step of the Synthesis of a Carbacephem Derivative.

Abstract: A Novel Dieckmann-Type Cyclization, the Final Step of the Synthesis of a Carbacephem Derivative.-Upon treatment with sodium bis(trimethylsilyl)amide followed by triflic anhydride, the azetidinone (I) is cyclized forming the carbacephem derivative (III) as the sole product.-(NEYER, G.; UGI, I.; Synthesis (1991) 9, 743-744; Inst. Org. Chem. Tech. Univ. Muenchen, D-8046 Garching, Fed. Rep. Ger.; EN)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?