Vellalath S - Search Results

1

Enzymatic assembly of the salinosporamide γ-lactam-β-lactone anticancer warhead.

Bauman KD, Shende VV, Chen PY, Trivella DBB, Gulder TAM, Vellalath S, Romo D, Moore BS. Bauman KD, et al. Among authors: vellalath s. Nat Chem Biol. 2022 May;18(5):538-546. doi: 10.1038/s41589-022-00993-w. Epub 2022 Mar 21. Nat Chem Biol. 2022. PMID: 35314816 Free PMC article.

2

(-)-Homosalinosporamide A and Its Mode of Proteasome Inhibition: An X-ray Crystallographic Study.

Groll M, Nguyen H, Vellalath S, Romo D. Groll M, et al. Among authors: vellalath s. Mar Drugs. 2018 Jul 19;16(7):240. doi: 10.3390/md16070240. Mar Drugs. 2018. PMID: 30029468 Free PMC article.

3

Asymmetric Organocatalysis: The Emerging Utility of α,β-Unsaturated Acylammonium Salts.

Vellalath S, Romo D. Vellalath S, et al. Angew Chem Int Ed Engl. 2016 Nov 2;55(45):13934-13943. doi: 10.1002/anie.201602217. Epub 2016 Sep 21. Angew Chem Int Ed Engl. 2016. PMID: 27650693 Free PMC article. Review.

4

Multicomponent Enantioselective Synthesis of Tetrahydropyridazinones Employing Chiral α,β-Unsaturated Acylammonium Salts.

Kiledal SA, Jourdain R, Vellalath S, Romo D. Kiledal SA, et al. Among authors: vellalath s. Org Lett. 2021 Sep 3;23(17):6622-6627. doi: 10.1021/acs.orglett.1c02044. Epub 2021 Aug 26. Org Lett. 2021. PMID: 34436913

5

Direct catalytic asymmetric synthesis of N-heterocycles from commodity acid chlorides by employing α,β-unsaturated acylammonium salts.

Vellalath S, Van KN, Romo D. Vellalath S, et al. Angew Chem Int Ed Engl. 2013 Dec 16;52(51):13688-93. doi: 10.1002/anie.201306050. Epub 2013 Oct 31. Angew Chem Int Ed Engl. 2013. PMID: 24173690

6

Enantioselective Synthesis of Medium-Sized Lactams via Chiral α,β-Unsaturated Acylammonium Salts.

Kang G, Yamagami M, Vellalath S, Romo D. Kang G, et al. Among authors: vellalath s. Angew Chem Int Ed Engl. 2018 May 28;57(22):6527-6531. doi: 10.1002/anie.201802483. Epub 2018 May 2. Angew Chem Int Ed Engl. 2018. PMID: 29624841

7

Formal reductive addition of acetonitrile to aldehydes and ketones.

Muratov K, Kuchuk E, Vellalath S, Afanasyev OI, Moskovets AP, Denisov G, Chusov D. Muratov K, et al. Among authors: vellalath s. Org Biomol Chem. 2018 Nov 7;16(41):7693-7701. doi: 10.1039/c8ob01992d. Epub 2018 Oct 5. Org Biomol Chem. 2018. PMID: 30288533

8

The catalytic asymmetric acetalization.

Kim JH, Čorić I, Vellalath S, List B. Kim JH, et al. Among authors: vellalath s. Angew Chem Int Ed Engl. 2013 Apr 15;52(16):4474-7. doi: 10.1002/anie.201300120. Epub 2013 Mar 19. Angew Chem Int Ed Engl. 2013. PMID: 23512823 No abstract available.

9

N-phosphinyl phosphoramide--a chiral Brønsted acid motif for the direct asymmetric N,O-acetalization of aldehydes.

Vellalath S, Corić I, List B. Vellalath S, et al. Angew Chem Int Ed Engl. 2010 Dec 10;49(50):9749-52. doi: 10.1002/anie.201005347. Angew Chem Int Ed Engl. 2010. PMID: 21064072 No abstract available.

10

N-heterocyclic carbene catalyzed reaction of enals and 1,2-dicarbonyl compounds: stereoselective synthesis of spiro gamma-butyrolactones.

Nair V, Vellalath S, Poonoth M, Mohan R, Suresh E. Nair V, et al. Among authors: vellalath s. Org Lett. 2006 Feb 2;8(3):507-9. doi: 10.1021/ol052926n. Org Lett. 2006. PMID: 16435871

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