Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Murugaiah, A M Subbaiah"'
Publikováno v:
Green Chemistry. 25:2368-2377
We report a metal catalyst-free, HF-free and open-flask green protocol for the electrophilic hydrazination of enoxy silanes at an energy-efficient room temperature, taking advantage of the eco-safe EtOH–H2O solvent.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74e6b88ca59caa1967db027d43ab5425
https://doi.org/10.1039/d2gc04607e
https://doi.org/10.1039/d2gc04607e
Publikováno v:
The Journal of Organic Chemistry. 87:14778-14792
Synthetically important α-oxoketene aminal intermediates can now be accessed from readily available and inexpensive carbodiimides as starting materials via the nucleophilic addition of palladium enolates derived from enol silane precursors. This ope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90f7b8fd5130aa467a525b6a3bda2b15
https://doi.org/10.1021/acs.joc.2c02107
https://doi.org/10.1021/acs.joc.2c02107
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd4b98e419d0b2015bda6099dfc0eb2d
https://doi.org/10.1021/acs.joc.3c00502
https://doi.org/10.1021/acs.joc.3c00502
Publikováno v:
The Journal of organic chemistry. 87(21)
The scope of an umpolung approach to expand synthetic access to bifunctional γ-keto hydrazine intermediates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99501ed7cfad9a7267b0dea82a0aeb5f
https://pubmed.ncbi.nlm.nih.gov/36190309
https://pubmed.ncbi.nlm.nih.gov/36190309
Publikováno v:
Journal of Medicinal Chemistry. 64:14046-14128
The benzene moiety is the most prevalent ring system in marketed drugs, underscoring its historic popularity in drug design either as a pharmacophore or as a scaffold that projects pharmacophoric elements. However, introspective analyses of medicinal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5ac2ef7ec0f24171683257ae23e25e5
https://doi.org/10.1021/acs.jmedchem.1c01215
https://doi.org/10.1021/acs.jmedchem.1c01215
Publikováno v:
The Journal of Organic Chemistry. 86:14356-14370
In contrast to the conventional 1,4-addition process, regioselective 1,2-addition of silyl enol ethers to quinones can now be achieved via a palladium(II) enolate pathway that provides access to 4-hydroxy-4-(2-oxo-2-arylethyl)cyclohexa-2,5-dien-1-one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33a6b0bb652aaf601028f122be4258f3
https://doi.org/10.1021/acs.joc.1c00857
https://doi.org/10.1021/acs.joc.1c00857
Autor:
Murugaiah, A M Subbaiah, Lakshumanan, Subramani, Thangeswaran, Ramar, Salil, Desai, Sarmistha, Sinha, Sandhya, Mandlekar, John F, Kadow, Susan, Jenkins, Mark, Krystal, Murali, Subramanian, Srikanth, Sridhar, Shweta, Padmanabhan, Priyadeep, Bhutani, Rambabu, Arla, Nicholas A, Meanwell
Publikováno v:
Journal of medicinal chemistry. 65(16)
Structure-property relationships associated with a series of (carbonyl)oxyalkyl amino acid ester prodrugs of the marketed HIV-1 protease inhibitor atazanavir (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e708bfe7b3076c0aafd6bdaec770723a
https://pubmed.ncbi.nlm.nih.gov/35952307
https://pubmed.ncbi.nlm.nih.gov/35952307
Autor:
Siddheshwar Kisan Chauthe, Anuradha Gupta, Muralidhararao Bagadi, Lakshumanan Subramani, Murugesan Shyamsundar, Lakshmikant Bajpai, Arvind Mathur, Murugaiah A. M. Subbaiah
Publikováno v:
SEPARATION SCIENCE PLUS. 4:16-23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::128ec375fba46bac7a03420b3a43df0d
https://doi.org/10.1002/sscp.202000046
https://doi.org/10.1002/sscp.202000046
Publikováno v:
The Journal of organic chemistry. 87(7)
The scope of chemoselective β-hydride elimination in the context of arylation/alkenylation of homoenolates from cyclopropanol precursors using organoboronic reagents as transmetalation coupling partners was examined. The reaction optimization paradi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e785f3ac00de1759eb9ac240a9977f3
https://pubmed.ncbi.nlm.nih.gov/35289619
https://pubmed.ncbi.nlm.nih.gov/35289619
Publikováno v:
The Journal of organic chemistry. 85(12)
Organoborane reagents were investigated as coupling partners to cyclopropanol-derived β-ketone enolates in the presence of a chelated Pd(II) catalyst. Efficient coupling of a range of electronically and sterically diverse cyclopropanols and aryl/alk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6488e950433c30ab8020bf7d81618f9d
https://pubmed.ncbi.nlm.nih.gov/32519863
https://pubmed.ncbi.nlm.nih.gov/32519863