Substrate-Directed Diastereoselective Hydroformylation of Methallylic Alcohols. -An effective directing metal-coordinating group is required for the diastereoselective hydroformylation. A key auxiliary is the Dpb group. Thus, the educts lead by catalytic hydroformylation to syn-aldehydes in very hi
ChemInform Abstract: Diastereoselective Hydroformylation of Certain Protected Allylic Alcohols.
β Scribed by T. DOI; H. KOMATSU; K. YAMAMOTO
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Substrate Directed Diastereoselective Hydroformylation of Acyclic Homomethallylic Alcohols. -Diastereoselective hydroformylation of acyclic alcohols is achieved with the aid of a catalyst-directing group. In all cases the corresponding aldehydes are formed in good yields with high anti-selectivity.
## 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 βFull Textβ option. The original article is trackable v
Substrate-Directed Diastereoselective Hydroformylation. Part 1. Substrate-Directed Diastereoselective Hydroformylation of Methallylic Alcohols -Development of an Efficient Catalyst-Directing Group for Rhodium-Catalyzed Hydroformylation. -The protection of methallylic alcohols (I) with the o-( diphen
## 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 βFull Textβ option. The original article is trackable v