Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Thondikkal Sulfikarali"'
Autor:
Jayaprakash, Ajay, Jha, Vikas Kumar, Krishnapriya, Vilakkathala U., Sanil, Gana, Thondikkal, Sulfikarali, Krishnan, Gayathri, Suresh, Cherumuttathu H., Iyer, E. Siva Subramaniam, Gokulnath, Sabapathi
Publikováno v:
ACS Applied Bio Materials; 10/25/2024, Vol. 7 Issue 10, p2146-2155, 10p
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 27:190-200
In this study, we have prepared new tripyrranes embedded with azulene bearing two meso-pentafluorophenyl substituents. They were obtained as diastereomers in high yield which were separated using conventional column chromatography. Their distinct sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d7312eeb1d34ed46a0aa82902de0228
https://doi.org/10.1142/s1088424622500808
https://doi.org/10.1142/s1088424622500808
Publikováno v:
Organic Letters. 24:1000-1004
Two conformationally different [26]rubyrin(1.1.0.1.1.0) macrocycles with varying heteroatoms (S/O) and their bis-BODIPYs are reported. The solid-state structure confirms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84ded4ce627bed0a9160747db0a4c0e9
https://doi.org/10.1021/acs.orglett.1c04043
https://doi.org/10.1021/acs.orglett.1c04043
Autor:
Thondikkal Sulfikarali, Govind Behera, Jayaprakash Ajay, Shigeki Mori, Akhil Chakravarthy Kakarlamudi, Sivaranjana Reddy Vennapusa, Sabapathi Gokulnath
Publikováno v:
Organic Letters. 24:245-249
1,4-Phenylene-linked cyclotrimer (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bf82694f74362a34e761dd316d628ed
https://doi.org/10.1021/acs.orglett.1c03903
https://doi.org/10.1021/acs.orglett.1c03903
Autor:
Jayaprakash Ajay, George Mariya Sandra, Masatoshi Ishida, Sabapathi Gokulnath, Thondikkal Sulfikarali
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 25:1143-1151
A simple rigid precursor termed as a “diheterole” bearing thiophene linked to [Formula: see text]-pyrrole at 4-position was prepared using a three-step synthetic strategy. This functionalized diheterole was allowed to undergo acid-catalyzed conde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::264317ab14e342efcc39fba3b07a668e
https://doi.org/10.1142/s108842462150108x
https://doi.org/10.1142/s108842462150108x
Autor:
Sabapathi Gokulnath, Thondikkal Sulfikarali, Kakarlamudi Akhil Chakravarthy, Jayaprakash Ajay, Vennapusa Sivaranjana Reddy
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 25:484-492
A simple non-rigid precursor termed as a “triheterole” comprising of 2,2[Formula: see text]-bithiophene linked to [Formula: see text]-pyrrole was prepared using a four-step synthetic strategy. This functionalized triheterole was allowed to underg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4183bd6d89d0e16bea6e3bd5736d6a9f
https://doi.org/10.1142/s1088424621500322
https://doi.org/10.1142/s1088424621500322
Autor:
Jayaprakash Ajay, Cherumuttathu H. Suresh, Sabapathi Gokulnath, Thondikkal Sulfikarali, Padinjare Veetil Bijina
Publikováno v:
The Journal of Organic Chemistry. 85:8021-8028
Acid-catalyzed condensation of a newly prepared di-m-benzipentapyrrane with appropriate mono- and diheterocyclic dialcohols selectively produced stable di-m-benzihexaphyrins and di-m-benziheptaphyrins with only two meso-carbon bridges. Single-crystal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::984fcab300c7693a7a362a3219ad263c
https://doi.org/10.1021/acs.joc.0c00754
https://doi.org/10.1021/acs.joc.0c00754
Autor:
Thondikkal, Sulfikarali, Jayaprakash, Ajay, Cherumuttathu H, Suresh, Padinjare V, Bijina, Sabapathi, Gokulnath
Publikováno v:
The Journal of organic chemistry. 85(12)
Acid-catalyzed condensation of a newly prepared di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22839af950be8610ed184740515ce6c6
https://pubmed.ncbi.nlm.nih.gov/32390421
https://pubmed.ncbi.nlm.nih.gov/32390421