1963
DOI: 10.1021/ja00906a008
|View full text |Cite
|
Sign up to set email alerts
|

Proximity Effects. XXXVII. Proximity Effects in the Solvolysis of 1-Octene Oxide

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1967
1967
2002
2002

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 6 publications
(1 citation statement)
references
References 0 publications
0
1
0
Order By: Relevance
“…This type of alternative was proposed to account for small proportions (<I%) of 1,3-, 1,4-, etc. diols formed in the solvolysis of 1-octene oxide (4). Nevertheless, such shifts are likely to be rare in acyclic systems (5), because of the proximity requirement for orbital overlap, in contrast to their prominence in alicyclic systems that offer suitable geometry (e.g., see ref.…”
Section: Modes Of Deuterium Incorporationmentioning
confidence: 99%
“…This type of alternative was proposed to account for small proportions (<I%) of 1,3-, 1,4-, etc. diols formed in the solvolysis of 1-octene oxide (4). Nevertheless, such shifts are likely to be rare in acyclic systems (5), because of the proximity requirement for orbital overlap, in contrast to their prominence in alicyclic systems that offer suitable geometry (e.g., see ref.…”
Section: Modes Of Deuterium Incorporationmentioning
confidence: 99%