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Synthesis of a new class of pyrazolyl-1,2,4-triazole amine derivatives.

• Authors : Reddy, N. Bakthavatchala; Durgamma, S.; Zyryanov, Grigory V.

Subjects: AMINE derivatives; MOIETIES (Chemistry); ALKENES

• Source: AIP Conference Proceedings; 2022, Vol. 2390 Issue 1, p1-4, 4p

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Synthesis of a New Class of Heteroaryl Dipyrazolyl Carbothioamides and Heteroaryl Dipyrazolyl Thiazoles and Evaluation as Antioxidants.

• Authors : Nagarjuna, Ummadi; Sravya, Gundala; Durgamma, S.

Subjects: AROMATIC compound synthesis; THIOAMIDES; THIAZOLES

• Source: AIP Conference Proceedings; 2019, Vol. 2063 Issue 1, p040039-1-040039-5, 5p, 1 Diagram

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Staudinger/aza-Wittig reaction to access Nβ-protected amino alkyl isothiocyanates.

• Authors : Santhosh, L.; Durgamma, S.; Shekharappa

• Source: Organic & Biomolecular Chemistry; 7/14/2018, Vol. 16 Issue 26, p4874-4880, 7p

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Facile one-pot synthesis of 2-amino-1,3,4-oxadiazole tethered peptidomimetics by molecular-iodine-mediated cyclodeselenization.

• Authors : Santhosh, L.; Srinivasulu, C.; Durgamma, S.

Subjects: PEPTIDOMIMETICS; OXADIAZOLES; PEPTIDE analysis

• Source: New Journal of Chemistry; 10/7/2017, Vol. 41 Issue 19, p11225-11229, 5p

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Synthesis of N β -Protected Amino Sulfenyl Methyl Formamides and Sulfonyl Methyl Formamides: A Simple Protocol.

• Authors : Srinivasulu C; Peptide Research Laboratory, Department of Chemistry, Jnana Bharathi, Bangalore University, Bengaluru 560056, India.; Sagar NR

• Source: ACS omega [ACS Omega] 2021 Feb 10; Vol. 6 (7), pp. 4680-4686. Date of Electronic Publication: 2021 Feb 10 (Print Publication: 2021).Publisher: American Chemical Society Country of Publication: United States NLM ID: 101691658 Publication Model: eCollection Cited Medium: Internet

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Staudinger/aza-Wittig reaction to access N β -protected amino alkyl isothiocyanates.

• Authors : Santhosh L; # 109, Peptide Research Laboratory, Department of Studies in Chemistry, Central College Campus, Dr. B. R. Ambedkar Veedhi, Bangalore University, Bangalore, 560001, India. .; Durgamma S

• Source: Organic & biomolecular chemistry [Org Biomol Chem] 2018 Jul 04; Vol. 16 (26), pp. 4874-4880.Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101154995 Publication Model: Print Cited Medium: Internet ISSN:

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