Unknown

Dataset Information

0

Stereodivergent synthesis of enantioenriched 4-hydroxy-2-cyclopentenones.


ABSTRACT: Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemical synthesis. A route to this class of compound has been developed. Key steps include Noyori reduction (which establishes the stereochemistry of the product), ring-closing metathesis, and simple functional group conversions to provide a set of substituted 4-HCPs in either enantiomeric form.

SUBMITTER: Singh G 

PROVIDER: S-EPMC3941174 | biostudies-literature | 2014 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Stereodivergent synthesis of enantioenriched 4-hydroxy-2-cyclopentenones.

Singh Gurpreet G   Meyer Angelica A   Aubé Jeffrey J  

The Journal of organic chemistry 20131220 1


Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemical synthesis. A route to this class of compound has been developed. Key steps include Noyori reduction (which establishes the stereochemistry of the product), ring-closing metathesis, and simple functional group conversions to provide a set of substituted 4-HCPs in either enantiomeric form. ...[more]

Similar Datasets

| S-EPMC5347846 | biostudies-literature
| S-EPMC9067570 | biostudies-literature
| S-EPMC7029798 | biostudies-literature
| S-EPMC3436603 | biostudies-literature
| S-EPMC4844805 | biostudies-literature
| S-EPMC5968508 | biostudies-literature
| S-EPMC4182949 | biostudies-other
| S-EPMC6385856 | biostudies-other
| S-EPMC3306479 | biostudies-literature