150 related articles for article (PubMed ID: 36500222)
1. One-Pot Sequence of Staudinger/aza-Wittig/Castagnoli-Cushman Reactions Provides Facile Access to Novel Natural-like Polycyclic Ring Systems.
Lebedev R; Dar'in D; Kantin G; Bakulina O; Krasavin M
Molecules; 2022 Nov; 27(23):. PubMed ID: 36500222
[TBL] [Abstract][Full Text] [Related]
2. The Use of Aryl-Substituted Homophthalic Anhydrides in the Castagnoli-Cushman Reaction Provides Access to Novel Tetrahydroisoquinolone Carboxylic Acid Bearing an All-Carbon Quaternary Stereogenic Center.
Moshnenko N; Kazantsev A; Bakulina O; Dar'in D; Krasavin M
Molecules; 2022 Dec; 27(23):. PubMed ID: 36500582
[TBL] [Abstract][Full Text] [Related]
3. Imines with rare α-heteroatom substituted amine components generated
Paramonova P; Eliseev I; Dar'in D; Bakulina O
Org Biomol Chem; 2024 Feb; 22(8):1733-1744. PubMed ID: 38323438
[TBL] [Abstract][Full Text] [Related]
4. Mechanistic Investigation of Castagnoli-Cushman Multicomponent Reactions Leading to a Three-Component Synthesis of Dihydroisoquinolones.
Howard SY; Di Maso MJ; Shimabukuro K; Burlow NP; Tan DQ; Fettinger JC; Malig TC; Hein JE; Shaw JT
J Org Chem; 2021 Sep; 86(17):11599-11607. PubMed ID: 34351161
[TBL] [Abstract][Full Text] [Related]
5. Trifluoroethanol Promoted Castagnoli-Cushman Cycloadditions of Imines with Homophthalic Anhydride.
Bayles T; Guillou C
Molecules; 2022 Jan; 27(3):. PubMed ID: 35164109
[TBL] [Abstract][Full Text] [Related]
6. New reagent space and new scope for the Castagnoli-Cushman reaction of oximes and 3-arylglutaconic anhydrides.
Bannykh A; Levashova E; Bakulina O; Krasavin M
Org Biomol Chem; 2022 Nov; 20(44):8643-8648. PubMed ID: 36281787
[TBL] [Abstract][Full Text] [Related]
7. Skeletal Diversity in Combinatorial Fashion: A New Format for the Castagnoli-Cushman Reaction.
Lepikhina A; Dar'in D; Bakulina O; Chupakhin E; Krasavin M
ACS Comb Sci; 2017 Nov; 19(11):702-707. PubMed ID: 29019643
[TBL] [Abstract][Full Text] [Related]
8. Further Insight into the Castagnoli-Cushman-type Synthesis of 1,4,6-Trisubstituted 1,6-Dihydropyridin-2-(3
Firsov A; Bakulina O; Dar'in D; Guranova N; Krasavin M
J Org Chem; 2020 May; 85(10):6822-6829. PubMed ID: 32338899
[TBL] [Abstract][Full Text] [Related]
9. Unexpected formal [4 + 2]-cycloaddition of chalcone imines and homophthalic anhydrides: preparation of dihydropyridin-2(1
Guranova N; Golubev P; Bakulina O; Dar'in D; Kantin G; Krasavin M
Org Biomol Chem; 2021 May; 19(17):3829-3833. PubMed ID: 33949583
[TBL] [Abstract][Full Text] [Related]
10. Beyond the Five and Six: Evaluation of Seven-Membered Cyclic Anhydrides in the Castagnoli-Cushman Reaction.
Adamovskyi MI; Ryabukhin SV; Sibgatulin DA; Rusanov E; Grygorenko OO
Org Lett; 2017 Jan; 19(1):130-133. PubMed ID: 28001424
[TBL] [Abstract][Full Text] [Related]
11. Unusually Reactive Cyclic Anhydride Expands the Scope of the Castagnoli-Cushman Reaction.
Chizhova M; Khoroshilova O; Dar'in D; Krasavin M
J Org Chem; 2018 Oct; 83(20):12722-12733. PubMed ID: 30226770
[TBL] [Abstract][Full Text] [Related]
12. A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-
Bakulina O; Ivanov A; Suslonov V; Dar'in D; Krasavin M
Beilstein J Org Chem; 2017; 13():1413-1424. PubMed ID: 28781707
[TBL] [Abstract][Full Text] [Related]
13. Extending the Scope of the New Variant of the Castagnoli-Cushman Cyclocondensation onto
Guranova N; Yakovleva L; Bakulina O; Dar'in D; Krasavin M
Molecules; 2022 Oct; 27(21):. PubMed ID: 36364037
[TBL] [Abstract][Full Text] [Related]
14. The Castagnoli-Cushman Reaction.
Ramiro JL; Martínez-Caballero S; Neo AG; Díaz J; Marcos CF
Molecules; 2023 Mar; 28(6):. PubMed ID: 36985626
[TBL] [Abstract][Full Text] [Related]
15. One-step route to tricyclic fused 1,2,3,4-tetrahydroisoquinoline systems via the Castagnoli-Cushman protocol.
Pashev A; Burdzhiev N; Stanoeva E
Beilstein J Org Chem; 2020; 16():1456-1464. PubMed ID: 32647547
[TBL] [Abstract][Full Text] [Related]
16. Toward lead-oriented synthesis: one-pot version of Castagnoli condensation with nonactivated alicyclic anhydrides.
Ryabukhin SV; Panov DM; Granat DS; Ostapchuk EN; Kryvoruchko DV; Grygorenko OO
ACS Comb Sci; 2014 Mar; 16(3):146-53. PubMed ID: 24479637
[TBL] [Abstract][Full Text] [Related]
17.
Paramonova P; Lebedev R; Bakulina O; Dar'in D; Krasavin M
Org Biomol Chem; 2022 Dec; 20(48):9679-9683. PubMed ID: 36412083
[TBL] [Abstract][Full Text] [Related]
18. De novo synthesis of sugar-aza-crown ethers via a domino Staudinger aza-Wittig reaction.
Ménand M; Blais JC; Valéry JM; Xie J
J Org Chem; 2006 Apr; 71(8):3295-8. PubMed ID: 16599634
[TBL] [Abstract][Full Text] [Related]
19. Cyclic Hydroxamic Acid Analogues of Bacterial Siderophores as Iron-Complexing Agents prepared through the Castagnoli-Cushman Reaction of Unprotected Oximes.
Bakulina O; Bannykh A; Dar'in D; Krasavin M
Chemistry; 2017 Dec; 23(70):17667-17673. PubMed ID: 29072340
[TBL] [Abstract][Full Text] [Related]
20. Synthesis of γ-Sultam-Annelated δ-Lactams via the Castagnoli-Cushman Reaction of Sultam-Based Dicarboxylic Acids.
Firsov A; Bakulina O; Dar'in D; Sokolov VV; Krasavin M
J Org Chem; 2022 Jan; 87(2):1537-1540. PubMed ID: 35000381
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
