1996
DOI: 10.1016/0040-4039(96)00083-4
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of substituted phenols Via photoaddition-fragmentation-aromatic annelation sequence

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1996
1996
2016
2016

Publication Types

Select...
3
2

Relationship

0
5

Authors

Journals

citations
Cited by 6 publications
(1 citation statement)
references
References 14 publications
0
1
0
Order By: Relevance
“…The intramolecular [2 + 2] photocycloaddition of 2,3-dihydro-4 H -pyran-4-ones was applied by Haddad and Salman to the synthesis of (+)-ligudentatol. More recently, Porco Jr. and co-workers employed the intramolecular [2 + 2] photocycloaddition of the pyran-2,4-dione rac - 266 to elucidate its constitution and relative configuration via a crystal structure of product rac - 267 (Scheme ). …”
Section: Direct Excitation and Sensitizationmentioning
confidence: 99%
“…The intramolecular [2 + 2] photocycloaddition of 2,3-dihydro-4 H -pyran-4-ones was applied by Haddad and Salman to the synthesis of (+)-ligudentatol. More recently, Porco Jr. and co-workers employed the intramolecular [2 + 2] photocycloaddition of the pyran-2,4-dione rac - 266 to elucidate its constitution and relative configuration via a crystal structure of product rac - 267 (Scheme ). …”
Section: Direct Excitation and Sensitizationmentioning
confidence: 99%