115 related articles for article (PubMed ID: 23460025)
1. The Staudinger reaction with 2-imino-1,3-thiaselenanes toward the synthesis of C4 spiro-β-lactams.
Toyoda Y; Ninomiya M; Ebihara M; Koketsu M
Org Biomol Chem; 2013 Apr; 11(16):2652-9. PubMed ID: 23460025
[TBL] [Abstract][Full Text] [Related]
2. The mechanism of the ketene-imine (staudinger) reaction in its centennial: still an unsolved problem?
Cossío FP; Arrieta A; Sierra MA
Acc Chem Res; 2008 Aug; 41(8):925-36. PubMed ID: 18662024
[TBL] [Abstract][Full Text] [Related]
3. Sequential Diimination, Staudinger [2 + 2] Ketene-Imine Cycloaddition, and Ring-Closing Metathesis (RCM) Reactions: In Route to Bis(4-spiro-fused-β-lactams)-Based Macrocycles.
Habib OM; Mohamed AS; Ibrahim YA; Al-Awadi NA
J Org Chem; 2021 Nov; 86(21):14777-14785. PubMed ID: 34609859
[TBL] [Abstract][Full Text] [Related]
4. Annuloselectivity in cycloadditions of ketenes with imines: a DFT study.
Li X; Xu J
J Org Chem; 2013 Jan; 78(2):347-55. PubMed ID: 23267672
[TBL] [Abstract][Full Text] [Related]
5. Dispirooxindole-β-Lactams: Synthesis via Staudinger Ketene-Imine Cycloaddition and Biological Evaluation.
Filatov VE; Iuzabchuk DA; Tafeenko VA; Grishin YK; Roznyatovsky VA; Lukianov DA; Fedotova YA; Sukonnikov MA; Skvortsov DA; Zyk NV; Beloglazkina EK
Int J Mol Sci; 2022 Jun; 23(12):. PubMed ID: 35743110
[TBL] [Abstract][Full Text] [Related]
6. Enantiomerically pure polyheterocyclic spiro-beta-lactams from trans-4-hydroxy-L-proline.
Cremonesi G; Dalla Croce P; Fontana F; La Rosa C
J Org Chem; 2010 Mar; 75(6):2010-7. PubMed ID: 20187611
[TBL] [Abstract][Full Text] [Related]
7. Access to Spiro Bis-β-lactams via a Metal-Free Microwave-Assisted Wolff Rearrangement/Staudinger [2+2] Cycloaddition Cascade Involving 3-Diazotetramic Acids and Imines.
Krivovicheva V; Lyutin I; Kantin G; Dar'in D
J Org Chem; 2024 Mar; 89(5):3585-3589. PubMed ID: 38363730
[TBL] [Abstract][Full Text] [Related]
8. Diastereoselective [2+2]-cycloaddition reactions of unsymmetrical cyclic ketenes with imines: synthesis of modified prolines and theoretical study of the reaction mechanism.
Macías A; Alonso E; Del Pozo C; Venturini A; González J
J Org Chem; 2004 Oct; 69(21):7004-12. PubMed ID: 15471445
[TBL] [Abstract][Full Text] [Related]
9. Chiral N-heterocyclic carbene catalyzed staudinger reaction of ketenes with imines: highly enantioselective synthesis of N-Boc beta-lactams.
Zhang YR; He L; Wu X; Shao PL; Ye S
Org Lett; 2008 Jan; 10(2):277-80. PubMed ID: 18085789
[TBL] [Abstract][Full Text] [Related]
10. Enantioselective Staudinger synthesis of beta-lactams catalyzed by a planar-chiral nucleophile.
Hodous BL; Fu GC
J Am Chem Soc; 2002 Feb; 124(8):1578-9. PubMed ID: 11853423
[TBL] [Abstract][Full Text] [Related]
11. Do reaction conditions affect the stereoselectivity in the Staudinger reaction?
Wang Y; Liang Y; Jiao L; Du DM; Xu J
J Org Chem; 2006 Sep; 71(18):6983-90. PubMed ID: 16930052
[TBL] [Abstract][Full Text] [Related]
12. Microwave- and photoirradiation-induced staudinger reactions of cyclic imines and ketenes generated from alpha-diazoketones. A further investigation into the stereochemical process.
Liang Y; Jiao L; Zhang S; Xu J
J Org Chem; 2005 Jan; 70(1):334-7. PubMed ID: 15624943
[TBL] [Abstract][Full Text] [Related]
13. Dicobalt hexacarbonyl complexes of alkynyl imines in a sequential Staudinger/Pauson-Khand process. A route to new fused tricyclic beta-lactams.
Olier C; Azzi N; Gil G; Gastaldi S; Bertrand MP
J Org Chem; 2008 Nov; 73(21):8469-73. PubMed ID: 18844409
[TBL] [Abstract][Full Text] [Related]
14.
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]
15. Asymmetric synthesis of anticancer beta-lactams via Staudinger reaction: utilization of chiral ketene from carbohydrate.
Banik BK; Banik I; Becker FF
Eur J Med Chem; 2010 Feb; 45(2):846-8. PubMed ID: 19962794
[TBL] [Abstract][Full Text] [Related]
16. Novel asymmetric approach to proline-derived spiro-beta-lactams.
Khasanov AB; Ramirez-Weinhouse MM; Webb TR; Thiruvazhi M
J Org Chem; 2004 Aug; 69(17):5766-9. PubMed ID: 15307755
[TBL] [Abstract][Full Text] [Related]
17. A versatile method for the synthesis of 3-alkoxycarbonyl beta-lactam derivatives.
Jiao L; Zhang Q; Liang Y; Zhang S; Xu J
J Org Chem; 2006 Jan; 71(2):815-8. PubMed ID: 16409001
[TBL] [Abstract][Full Text] [Related]
18. Notable and obvious ketene substituent-dependent effect of temperature on the stereoselectivity in the Staudinger reaction.
Li B; Wang Y; Du DM; Xu J
J Org Chem; 2007 Feb; 72(3):990-7. PubMed ID: 17253821
[TBL] [Abstract][Full Text] [Related]
19. Stereocontrolled synthesis of anticancer beta-lactams via the Staudinger reaction.
Banik BK; Banik I; Becker FF
Bioorg Med Chem; 2005 Jun; 13(11):3611-22. PubMed ID: 15862989
[TBL] [Abstract][Full Text] [Related]
20. [2 + 1 + 1] Assembly of spiro β-lactams by Rh(ii)-catalyzed reaction of diazocarbonyl compounds with azirines/isoxazoles.
Golubev AA; Smetanin IA; Agafonova AV; Rostovskii NV; Khlebnikov AF; Starova GL; Novikov MS
Org Biomol Chem; 2019 Jul; 17(28):6821-6830. PubMed ID: 31250875
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
