Page last updated: 2024-08-26

cyanates and oxazolidin-2-one

cyanates has been researched along with oxazolidin-2-one in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Ichikawa, Y; Kotsuki, H; Nakano, K; Yamaoka, T1
Hosotani, A; Lautens, M; Ninnemann, NM; Tsui, GC1
Hu, C; Khanna, K; Wu, J; Yin, Z; Zeng, H; Zhang, J; Zheng, S1
Adhikari, D; Baik, MH; Lord, RL; Nguyen, ST; Paddock, RL1
Bansagi, J; Batey, RA; Debrauwer, V; Narayanan, P; Wilson-Konderka, C1

Other Studies

5 other study(ies) available for cyanates and oxazolidin-2-one

ArticleYear
Synthesis of (-)-agelastatin A by [3.3] sigmatropic rearrangement of allyl cyanate.
    Organic letters, 2007, Aug-02, Volume: 9, Issue:16

    Topics: Alkaloids; Allyl Compounds; Catalysis; Cyanates; Molecular Structure; Oxazolidinones; Stereoisomerism; Sugar Alcohols

2007
Expedient synthesis of chiral oxazolidinone scaffolds via rhodium-catalyzed asymmetric ring-opening with sodium cyanate.
    Organic letters, 2013, Mar-01, Volume: 15, Issue:5

    Topics: Catalysis; Cyanates; Molecular Structure; Oxazolidinones; Rhodium; Stereoisomerism

2013
An expedient stereoselective and chemoselective synthesis of bicyclic oxazolidinones from quinols and isocyanates.
    Organic & biomolecular chemistry, 2013, May-14, Volume: 11, Issue:18

    Topics: Cyclization; Hydroquinones; Isocyanates; Molecular Structure; Oxazolidinones; Stereoisomerism

2013
[(Salcen)Cr(III) + Lewis base]-catalyzed synthesis of N-aryl-substituted oxazolidinones from epoxides and aryl isocyanates.
    Chemical communications (Cambridge, England), 2014, Dec-14, Volume: 50, Issue:96

    Topics: Catalysis; Chromium; Coordination Complexes; Cycloaddition Reaction; Epoxy Compounds; Isocyanates; Lewis Bases; Molecular Conformation; Oxazolidinones

2014
    The Journal of organic chemistry, 2022, 09-02, Volume: 87, Issue:17

    Topics: Alcohols; Amines; Biological Products; Carbamates; Hydantoins; Isocyanates; Oxazolidinones; Thiocarbamates; Urea

2022