Stereoselective synthesis of (3S,4R)- and (3R,4S)-4-(N-substituted-amino)- 2,2-dimethyl-6-nitrochroman-3-ols via the microwave assisted regioselective ring opening of epoxides in the presence of neutral alumina

Tetrahedron Asymmetry

Volumn 23, Issue 14, 2012, Pages 1029-1037

  Meng, Li Juan ^a   Vijaykumar, B V D ^a   Zuo, Hua ^b   Li, Zhu Bo ^b   Dupati, Gautam ^a   Jang, Kiwan ^a   Shin, Dong Soo ^a  

^a Changwon National University   (South Korea)

^b SOUTHWEST UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

2,2 DIMETHYL 6 NITRO 4 (4 NITROPHENYLAMINO)CHROMAN 3 OL; 2,2 DIMETHYL 6 NITRO 4 (PIPERIDIN 1 YL)CHROMAN 3 OL; 2,2 DIMETHYL 6 NITRO 4 1 PHENYLETHYLAMINO)CHROMAN 3 OL; 2,2 DIMETHYL 6 NITRO 4 [(TETRAHYDROFURAN 2 YL)METHYLAMINO)CHROMAN 3 OL ENT; 2,2 DIMETHYL 6 NITRO 4 [(TETRAHYDROFURAN 2 YL)METHYLAMINO]CHROMAN 3 OL; 4 (4 (4 METHOXYPHENYL)PIPERAZIN 1 YL) 2,2 DIMETHYL 6 NITROCHROMAN 3 OL; 4 (BENZYLAMINO) 2,2 DIMETHYL 6 NITROCHROMAN 3 OL; 4 (CYCLOHEXYLAMINO) 2,2 DIMETHYL 6 NITROCHROMAN 3 OL; 4 (CYCLOHEXYLMETHYLAMINO) 2,2 DIMETHYL 6 NITROCHROMAN 3 OL; 4 (DIMETHYLAMINO) 2,2 DIMETHYL 6 NITROCHROMAN 3 OL; 4 (HEXYLAMINO) 2,2 DIMETHYL 6 NITROCHROMAN 3 OL; 4 (N AMINO) 2,2 DIMETHYL 6 NITROCHROMAN 3 OL; CHROMAN DERIVATIVE; UNCLASSIFIED DRUG;

AMINOLYSIS; ARTICLE; EPOXIDATION; MICROWAVE RADIATION; PRIORITY JOURNAL; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION;

EID: 84865473130     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2012.07.002     Document Type: Article

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