Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Subba Rao Jammula"'
Autor:
Rajesh Jinkala, Shiva Kumar K. B., Venkateshwarlu Rapolu, Nikumbh Satish P., Subba Rao Jammula, Siddaiah Vidavalur, Ramamohan Hindupur, Krishnaji Tadiparthi, Akula Raghunadh
Publikováno v:
Synthetic Communications. 52:258-267
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a79c897ddc1e13b02416d550b0572816
https://doi.org/10.1080/00397911.2021.2019278
https://doi.org/10.1080/00397911.2021.2019278
Autor:
M. V. Madhubabu, Subba Rao Jammula, L. Vaikunta Rao, Akula Raghunadh, Krishnaji Tadiparthi, V. Narayana Murthy, Satish P. Nikumbh
Publikováno v:
RSC Advances. 8:22331-22334
A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a catalyst, giving good to moderate yields. In this reaction the substrate scope for amines and alde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5d73b4c9cf5d53c82d775374b204f26
https://doi.org/10.1039/c8ra03308k
https://doi.org/10.1039/c8ra03308k
Autor:
Venkateswara Rao Anna, B. Yogi Sreenivas, Thalishetti Krishna, Subba Rao Jammula, Sudhakar Tatina, Manojit Pal
Publikováno v:
Tetrahedron Letters. 57:3924-3928
A highly efficient synthesis of (S)-1-(furan-2-yl)pent-4-en-1-ol, known to be an initial precursor of Ipomoeassin family of compounds and C1–C15 domain of halichondrins has been achieved via a sequence involving the use of Weinreb amide formation f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75c0b34b9fc5c75b2760160227613aac
https://doi.org/10.1016/j.tetlet.2016.07.059
https://doi.org/10.1016/j.tetlet.2016.07.059
Autor:
Hanumiah Telikepalli, Subba Rao Jammula, K.V.Jagannadha Rao, Sridhara Babu Pepalla, Ronald H. Thomson
Publikováno v:
Phytochemistry. 30:3741-3744
From the acetone extract of the root bark of Ventilago goughii four new benzisochromanquinones, ventiloquinones L, M, N and O have been isolated. The structures of ventiloquinone-L as cis -9-hydroxy-7-methoxy-1,3-dimethyl-3,4,5,10-tetrahydro-1 H -nap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7866d7bccb069eb0abf2942862a80f2
https://doi.org/10.1016/0031-9422(91)80100-f
https://doi.org/10.1016/0031-9422(91)80100-f
Autor:
Ecaterina Misilim, Georgeta Cernaianu, Subba Rao Jammula, Shimon Oami, Anatoly Leytin, Francine R. Dembitzer, D. Stave Kohtz, Caryn Chu, James A. Strauchen, David Burstein
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 15(7)
Monoclonal antibody 12D11 (MAb 12D11) has been shown to bind histone H1 isolated from human placenta and other tissues but not histone H1 that has been digested with bacterial alkaline phosphatase. We show here that phosphorylation of phosphatase-tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd06ff53d9a205266ace211ecebe823
https://pubmed.ncbi.nlm.nih.gov/12118107
https://pubmed.ncbi.nlm.nih.gov/12118107
Publikováno v:
Phytochemistry. 31:2103-2104
Seventeen compounds have been isolated from the acetone extract of the stem bark of Ventilago bombaiensis . They were identified as chrysophanol, 10-(chrysophanol-7′-yl)-10-hydroxychrysophanol-9-anthrone, chrysophanol 8-methyl ether, citreorosein,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65606363cc7d7730f79ec7932c851bd6
https://doi.org/10.1016/0031-9422(92)80371-k
https://doi.org/10.1016/0031-9422(92)80371-k
Autor:
Subba Rao Jammula, Kolluru Venkata Jagannadha Rao, Kesava Rao Bhattiprolu, Sridhara Babu Pepalla, Hanumaiah Telikepalli
Publikováno v:
Phytochemistry. 30:4193-4194
A new naphthalene glucoside lactone was isolated from the acetone extract of the stem bark of Rhamnus wightii . Cynodontin, chrysophanol, physcion, musizin, lupeol, sitosterol, 7-hydroxy-5-methoxyphthalide, emodin, sitosterol glycoside, β-sorigenin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b84fa65d90475c3324e315eb721976
https://doi.org/10.1016/0031-9422(91)83502-c
https://doi.org/10.1016/0031-9422(91)83502-c