## Abstract A one‐flask reaction sequence comprising ring closing metathesis (RCM) of butenoates derived from allylic alcohols and a base‐mediated ring opening gives 2__Z__,4__E__‐configured dienoic acids in high yields and stereoselectivities. Application of the method to the synthesis of the natu
ChemInform Abstract: One-Flask Tethered Ring Closing Metathesis—Electrocyclic Ring Opening for the Highly Stereoselective Synthesis of Conjugated Z/E-Dienes.
✍ Scribed by Bernd Schmidt; Oliver Kunz
- Book ID
- 112045888
- Publisher
- John Wiley and Sons
- Year
- 2012
- Weight
- 40 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v