Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pavan Sudheer Akula"'
Publikováno v:
Organic Letters. 23:4688-4693
The organocatalytic α-alkylation of vinylogous carbonyl compounds to hydroxynitroolefins for the synthesis of hemiacetals was realized with excellent enantioselectivities and in high yields. High diastereoselectivity (up to >20:1) has been accomplis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ffc5b3753d4c4df3edb3b591bb9f4c8
https://doi.org/10.1021/acs.orglett.1c01426
https://doi.org/10.1021/acs.orglett.1c01426
Publikováno v:
Organic letters. 24(18)
First total synthesis of ulodione A has been achieved via the key-step reactions of DIPEA-promoted dialkytion of 1,3-cyclopentadione with a bromonitroolefin and DABCO promoted/catalytic semipinacol-like ring-expansion rearrangement, with regioselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b770be385b34df7f93386f6e4a8ce52
https://pubmed.ncbi.nlm.nih.gov/35499378
https://pubmed.ncbi.nlm.nih.gov/35499378
Publikováno v:
Organic Letters. 20:7835-7839
The first regioselective, diastereoselective, and enantioselective organocatalyzed Michael-Michael cascade of vinylogous ketone enolates and nitroalkenes for the construction of fully substituted cyclobutanes is achieved by the deployment of the appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1dd720046cc75473e1a1e879af07c3e
https://doi.org/10.1021/acs.orglett.8b03335
https://doi.org/10.1021/acs.orglett.8b03335
Publikováno v:
Organic letters. 22(1)
New types of organocatalytic 1,2-rearrangements, which resemble the Smiles-like or semi-pinacol-like rearrangement, of Michael adducts of 1,3-dicarbonyl-2-alkyl compounds and nitroalkenes have been realized. Unlike the well-known conjugate addition,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ad8a3042e86317c7e8d3c779f1d6c0f
https://pubmed.ncbi.nlm.nih.gov/31829018
https://pubmed.ncbi.nlm.nih.gov/31829018
Publikováno v:
Organic letters. 21(19)
A mild and convenient process for direct transformation of nitroalkanes to the corresponding nitriles was developed using a visible-light photoredox catalysis strategy with household decorative blue LEDs and the additives of Et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c346629dde2b668d44fe7d23f0cc456d
https://pubmed.ncbi.nlm.nih.gov/31513414
https://pubmed.ncbi.nlm.nih.gov/31513414
Publikováno v:
RSC advances. 8(35)
A convenient photocatalyzed oxidative coupling reaction of 4-alkyl-3,4-dihydroquinoxalin-2(1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c0099d23757cfc9efcd461fa79a18f21
https://pubmed.ncbi.nlm.nih.gov/35540997
https://pubmed.ncbi.nlm.nih.gov/35540997