1996
DOI: 10.1016/0040-4020(96)00887-3
|View full text |Cite
|
Sign up to set email alerts
|

Rearrangements of the 2,6-diaryl-3,7-dioxabicyclo[3.3.0] octane skeleton, part III. Reaction of gmelinol with BF3-etherate and N,N-dimethylaniline

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

1997
1997
2008
2008

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 10 publications
(1 citation statement)
references
References 7 publications
0
1
0
Order By: Relevance
“…3). The cis-orientation of HÀC (3) and HÀC(4) to each other was established from the coupling constant of HÀC(4) (J ¼ 6.5 Hz) by comparison with the values reported for cycloolivil (trans-orientation, J ¼ 10.0 Hz) [8] and di-O-methyl epicycloolivil (cis-orientation, J ¼ 5.5 Hz) [10]. In addition, the observed NOE correlations (Fig.…”
mentioning
confidence: 99%
“…3). The cis-orientation of HÀC (3) and HÀC(4) to each other was established from the coupling constant of HÀC(4) (J ¼ 6.5 Hz) by comparison with the values reported for cycloolivil (trans-orientation, J ¼ 10.0 Hz) [8] and di-O-methyl epicycloolivil (cis-orientation, J ¼ 5.5 Hz) [10]. In addition, the observed NOE correlations (Fig.…”
mentioning
confidence: 99%