Unknown

Dataset Information

0

Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.


ABSTRACT: Strained polycyclic oxetanes generated photochemically from the Diels-Alder adducts of cyclic dienes and enones undergo deep skeletal rearrangements under protolytic ring-opening conditions offering expeditious access to chlorohydrins and other products of unique skeletal topology.

SUBMITTER: Valiulin RA 

PROVIDER: S-EPMC2912957 | biostudies-literature | 2010 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.

Valiulin Roman A RA   Arisco Teresa M TM   Kutateladze Andrei G AG  

Organic letters 20100801 15


Strained polycyclic oxetanes generated photochemically from the Diels-Alder adducts of cyclic dienes and enones undergo deep skeletal rearrangements under protolytic ring-opening conditions offering expeditious access to chlorohydrins and other products of unique skeletal topology. ...[more]

Similar Datasets

| S-EPMC4793204 | biostudies-literature
| S-EPMC2756614 | biostudies-literature
| S-EPMC5930398 | biostudies-literature
| S-EPMC9310094 | biostudies-literature
| S-EPMC1383653 | biostudies-literature
| S-EPMC2837476 | biostudies-literature
| S-EPMC3600475 | biostudies-literature
| S-EPMC1863511 | biostudies-literature
| S-EPMC7776973 | biostudies-literature
| S-EPMC6204778 | biostudies-literature