Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jan Paciorek"'
Publikováno v:
Journal of the American Chemical Society. 144(43)
We report a general synthetic entry to dihydrooxepine-spiroisoxazoline (DOSI) natural products that culminated in the first racemic total synthesis of psammaplysin A. For the synthesis of the unique spirocyclic fragment we employed a strategy that fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e8268273b12ea95a8fe9b2148d1fcb5
https://pubmed.ncbi.nlm.nih.gov/36270001
https://pubmed.ncbi.nlm.nih.gov/36270001
Here, we report a general synthetic entry to dihydrooxepine-spiroisoxazoline (DOSI) natural products that culminated in the first total synthesis of psammaplysin A. For the synthesis of the unique spirocyclic fragment we employed a strategy that feat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::687c74e67c3a51aff1ca5756757423b4
https://doi.org/10.26434/chemrxiv-2022-px26h-v2
https://doi.org/10.26434/chemrxiv-2022-px26h-v2
Publikováno v:
The Journal of Organic Chemistry. 85:6992-7000
The mechanism of acetylene bromoboration in neat boron tribromide was studied carefully by means of experiment and theory. Besides the syn-addition mechanism through a four-center transition state,...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::766344ed2e4fcbd66cada2f20af4bbf9
https://doi.org/10.1021/acs.joc.0c00341
https://doi.org/10.1021/acs.joc.0c00341
Publikováno v:
The Journal of organic chemistry. 85(11)
The mechanism of acetylene bromoboration in neat boron tribromide was studied carefully by means of experiment and theory. Besides the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::77dce9761a205377dc44d7cf7ca83101
https://pubmed.ncbi.nlm.nih.gov/32436705
https://pubmed.ncbi.nlm.nih.gov/32436705