2003
DOI: 10.1039/b302460a
|View full text |Cite
|
Sign up to set email alerts
|

Total synthesis of the marine sponge metabolites (+)-rottnestol, (+)-raspailol A and (+)-raspailol BTaken in part from the PhD thesis of I. R. Czuba, The University of Melbourne, 2002.

Abstract: The asymmetric syntheses of (+)-rottnestol (1) and the related marine sponge metabolites (+)-raspailols A (5) and B (6) are described. The key step in each of these sequences was a Stille coupling to form the C9-C10 sp2-sp2 bond and connect the polyene sidechains to the appropriate optically active tetrahydropyran core. For rottnestol (1), both C12 epimers were synthesised by a coupling between stannane 7 and (R)- or (S)-8 followed by acid hydrolysis which allowed for the assignment of the absolute configurati… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
19
0

Year Published

2003
2003
2017
2017

Publication Types

Select...
6
3

Relationship

0
9

Authors

Journals

citations
Cited by 26 publications
(19 citation statements)
references
References 40 publications
0
19
0
Order By: Relevance
“…The route in Fig. 4 is more efficient than those disclosed previously (21.5% vs. 3.7% overall yield) 43 and which resulted in no more than milligram quantities of the target molecule.…”
Section: Gram Scale Total Synthesis Of Rottnestolmentioning
confidence: 65%
“…The route in Fig. 4 is more efficient than those disclosed previously (21.5% vs. 3.7% overall yield) 43 and which resulted in no more than milligram quantities of the target molecule.…”
Section: Gram Scale Total Synthesis Of Rottnestolmentioning
confidence: 65%
“…Condensation of the known 4 [6] and 5 [7] led to 6, which on saponification gave free acid 7. To this end, the C-23 ketone carbonyl group in 9 was setereoselectively reduced with Me 4 NB(OAc) 3 H [8] to afford 13 (Scheme 3). However, subsequent condensation of 7 with aldol subunit 9 (prepared as described before, Scheme 2) did not occur as reported [3] before.…”
Section: Resultsmentioning
confidence: 99%
“…129 The absolute configuration of the ring portion was determined by Mosher's method, but the full stereochemical assignment was only accomplished by total synthesis. 130 Although the crude sponge extract showed mild antibacterial activity, no activity has been reported for the pure compounds.…”
Section: Secondary Metabolites Reported From the Genus Raspailiamentioning
confidence: 99%