neorustmicin-a and allyl-alcohol

neorustmicin-a has been researched along with allyl-alcohol* in 1 studies

Other Studies

1 other study(ies) available for neorustmicin-a and allyl-alcohol

Article	Year
A total synthesis of galbonolide B. The Journal of organic chemistry, 2007, Nov-23, Volume: 72, Issue:24 An ester enolate rearrangement/silicon mediated fragmentation cascade was used to convert 7 and 8 into the alcohol 9. The alcohol 9 was converted into the allylic alcohol 12 and then to the ester 14. A further ester enolate rearrangement furnished the stereochemical identity of galbonolide B 1. Base mediated macrocyclization of the acetate ester 16 followed by base mediated alkylation and acetal deprotection gave galbonolide B 1. Topics: Acetals; Acetates; Alkylation; Antifungal Agents; Cyclization; Lactones; Models, Chemical; Propanols	2007

Article

Year

The Journal of organic chemistry, 2007, Nov-23, Volume: 72, Issue:24

An ester enolate rearrangement/silicon mediated fragmentation cascade was used to convert 7 and 8 into the alcohol 9. The alcohol 9 was converted into the allylic alcohol 12 and then to the ester 14. A further ester enolate rearrangement furnished the stereochemical identity of galbonolide B 1. Base mediated macrocyclization of the acetate ester 16 followed by base mediated alkylation and acetal deprotection gave galbonolide B 1.

Topics: Acetals; Acetates; Alkylation; Antifungal Agents; Cyclization; Lactones; Models, Chemical; Propanols

2007