Zobrazeno 1 - 10
of 227
pro vyhledávání: '"T V, RajanBabu"'
Publikováno v:
Dalton Transactions. 51:10148-10159
New synthesis of (L)[CoIX]-complexes from (L)CoX2 and Mashima's reagent.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bd9ebb9185f6850222750151de84677
https://doi.org/10.1039/d2dt01484j
https://doi.org/10.1039/d2dt01484j
Autor:
Stanley M. Jing, Vinayak Vishnu Pagar, Mahesh M. Parsutkar, Souvagya Biswas, T. V. RajanBabu, James H. Herbort
Publikováno v:
Acc Chem Res
ConspectusOne of the major challenges facing organic synthesis in the 21st century is the utilization of abundantly available feedstock chemicals for fine chemical synthesis. Regio- and enantioselective union of easily accessible 1,3-dienes and other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3cb6d94291c33c9635096cacc583434
https://doi.org/10.1021/acs.accounts.1c00573
https://doi.org/10.1021/acs.accounts.1c00573
Autor:
Dipshi Singh, T. V. RajanBabu
Publikováno v:
Angewandte Chemie International Edition. 62
Alkynes and 1,3-dienes are among the most readily available precursors for organic synthesis. We report two distinctly different, catalyst-dependent, modes of regio- and enantioselective cycloaddition reactions between these classes of compounds prov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::267b9d692dc9586b60383cbcf7fa5b96
https://doi.org/10.1002/anie.202216000
https://doi.org/10.1002/anie.202216000
Publikováno v:
ACS Catal
(E)-2-Trialkylsilyloxy-1,3-dienes and the corresponding 2-acetoxy derivatives participate in cobalt-catalyzed heterodimerization reactions with ethylene, giving mostly 4,1-hydrovinylation products with addition of the vinyl group to C(4) and H at C(1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9d2f98302f2e88a79b2eb548807c7e2
https://pubmed.ncbi.nlm.nih.gov/36110156
https://pubmed.ncbi.nlm.nih.gov/36110156
Publikováno v:
ACS Catalysis. 11:9605-9617
Two intermolecular hydroalkenylation reactions of 1,6-enynes are presented which yield substituted 5-membered carbo- and -heterocycles. This reactivity is enabled by a cationic bis-diphenylphosphinopropane (DPPP)CoI species which forms a cobaltacyclo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78d1104790c7754dc1876f06fd9bdc26
https://doi.org/10.1021/acscatal.1c02530
https://doi.org/10.1021/acscatal.1c02530
Autor:
Bill Nugent, T. V. RajanBabu
Publikováno v:
Angewandte Chemie. 133:2222-2229
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af5bdff291c0f5f5c29ed5f3d330545d
https://doi.org/10.1002/ange.202011838
https://doi.org/10.1002/ange.202011838
Autor:
William A. Nugent, T. V. RajanBabu
Publikováno v:
Angew Chem Int Ed Engl
While writing a comprehensive review on the reactions of epoxides with titanium(III) reagents, we encountered a series of mechanistic puzzles. Using clues from the literature, many of which were not available at the time that the mysteries emerged, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3edfa66cc6df0b1eae007b4166e0d2c1
https://doi.org/10.1002/anie.202011838
https://doi.org/10.1002/anie.202011838
Publikováno v:
ACS catalysis. 11(15)
Two intermolecular hydroalkenylation reactions of 1,6-enynes are presented which yield substituted 5-membered carbo- and -heterocycles. This reactivity is enabled by a cationic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9501a4b5034ac389b68ca297310ef6e1
https://pubmed.ncbi.nlm.nih.gov/34745711
https://pubmed.ncbi.nlm.nih.gov/34745711
Autor:
Mahesh M. Parsutkar, T. V. RajanBabu
Publikováno v:
J Am Chem Soc
Ketones are among the most widely used intermediates in organic synthesis, and their synthesis from inexpensive feedstocks could be quite impactful. Regio- and enantioselective hydroacylation reactions of dienes provide facile entry into useful keton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5135b025c46e69d8738cd7a5e88059c8
https://pubmed.ncbi.nlm.nih.gov/34351138
https://pubmed.ncbi.nlm.nih.gov/34351138
