Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pierre H. Storck"'
Autor:
Pierre H. Storck, Douglass F. Taber
Publikováno v:
The Journal of Organic Chemistry. 67:8273-8275
A one-pot preparation of unsymmetrical 1,4-alkynediols such as 2a by the coupling of trimethylsilylacetylene and two different aldehydes or ketones is reported. The dilithiated species 5 is generated by the sequential addition of the first aldehyde o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d61288625b788f4bb98c762557633996
https://doi.org/10.1021/jo020486x
https://doi.org/10.1021/jo020486x
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::419c507c09d27355b6cbaf769d49e0a4
https://doi.org/10.1002/chin.200741154
https://doi.org/10.1002/chin.200741154
Publikováno v:
The Journal of organic chemistry. 72(11)
The first enantioselective synthesis of a chamigrane sesquiterpene, (+)-majusculone, has been completed. The quaternary center was generated asymmetrically by alkylidene carbene insertion, with retention of absolute configuration, from a diastereomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63bdbc0dca42b163b2b639ff4b5f67ce
https://pubmed.ncbi.nlm.nih.gov/17447815
https://pubmed.ncbi.nlm.nih.gov/17447815
Autor:
Douglass F. Taber, Pierre H. Storck
Publikováno v:
The Journal of organic chemistry. 68(20)
The preparation of an advanced intermediate toward the enantioselective synthesis of tetrodotoxin is outlined. The enantiomerically pure cyclopentene 15 was generated from ketone 14 by alkylidene carbene insertion with retention of absolute configura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf934c4af757406c6a4401f6e5d23b50
https://pubmed.ncbi.nlm.nih.gov/14510553
https://pubmed.ncbi.nlm.nih.gov/14510553