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Volumn 66, Issue 52, 2010, Pages 9902-9911

Chiral amines in the diastereoselective Mannich-related multicomponent synthesis of diarylmethylamines, 1,2-diarylethylamines, and β- arylethylamines

Author keywords

Cobalt; Diastereoselectivity; Multicomponent reactions; Organozinc compounds; Zinc

Indexed keywords

1 (2 FLUOROPHENYL) 2 PHENYL N (1 PHENYLETHYL)ETHYLAMINE; 1 ALLYL 4 (1,2 DIPHENYLETHYL) 2,5 DIMETHYLPIPERAZINE; 1 PHENYL N (1 PHENYLETHYL) 2 (O TOLYL)ETHYLAMINE; 1,2 DIARYLETHYLAMINE DERIVATIVE; 1,2 DIPHENYL N (1 PHENYLETHYL)ETHYLAMINE; 2 PHENYL N (1 PHENYLETHYL) 1 (THIOPHEN 3 YL)ETHYLAMINE; ALDEHYDE; ALPHA METHYLBENZYLAMINE; AMINE; BENZALDEHYDE; BENZYLZINC BROMIDE; BETA ARYLETHYLAMINE DERIVATIVE; BROMINE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; DIARYLMETHYLAMINE DERIVATIVE; ETHYL 1 (1,2 DIPHENYLETHYL)PYRROLIDINE 2 CARBOXYLATE; ETHYL 3 PHENYL 2 [(1 PHENYLETHYL)AMINO] PROPANOATE; METHYL 1 [(3 METHOXYPHENYL)(PHENYL)METHYL] PYRROLIDINE 2 CARBOXYLATE; METHYL 1 [PHENYL (PYRIDIN 4 YL)METHYL] PYRROLIDINE 2 CARBOXYLATE; METHYL 1 [PHENYL [4 (M TOLYL)METHYL]] PYRROLIDINE 2 CARBOXYLATE; METHYL 1 [PHENYL [4 (TRIFLUOROMETHYL)PHENYL] METHYL] PYRROLIDINE 2 CARBOXYLATE; N [1 (NAPHTHALEN 2 YL)ETHYL] 1,2 DIPHENYLETHYLAMINE; PIPERAZINE DERIVATIVE; PROLINE; REAGENT; TRANS 1 ALLYL 2,5 DIMETHYLPIPERAZINE; UNCLASSIFIED DRUG;

EID: 78649653060     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.10.058     Document Type: Article
Times cited : (15)

References (96)
  • 1
    • 84890597202 scopus 로고    scopus 로고
    • Wiley-VCH Weinheim
    • For a reference book, see: J. Zhu, H. Bienaymé, Multicomponent Reactions 2005 Wiley-VCH Weinheim
    • (2005) Multicomponent Reactions
    • J. Zhu1
  • 2
    • 78649664784 scopus 로고    scopus 로고
    • For recent reviews on multicomponent reactions (MCRs) and asymmetric MCRs (AMCRs), see
    • For recent reviews on multicomponent reactions (MCRs) and asymmetric MCRs (AMCRs), see:
  • 39
    • 78649658752 scopus 로고    scopus 로고
    • For systems employing the Petasis reaction, see
    • For systems employing the Petasis reaction, see:
  • 62
    • 78649664021 scopus 로고    scopus 로고
    • A single experiment involving the use of 1-phenylethylamine had been disclosed, see Ref. 9c for details
    • A single experiment involving the use of 1-phenylethylamine had been disclosed, see Ref. 9c for details.
  • 65
    • 78649638022 scopus 로고    scopus 로고
    • Proline esters were obtained as hydrochlorides thus 3 equiv of the organozinc reagent were used
    • Proline esters were obtained as hydrochlorides thus 3 equiv of the organozinc reagent were used.
  • 77
    • 78649648158 scopus 로고    scopus 로고
    • For some miscellaneous examples, see
    • For some miscellaneous examples, see:
  • 87
    • 78649647359 scopus 로고    scopus 로고
    • One can envisage the possible use of e.g., 4-methoxybenzyl or 2,4-dimethoxybenzyl groups, which might be selectively removed by different pathways, for some miscellaneous examples see
    • One can envisage the possible use of e.g., 4-methoxybenzyl or 2,4-dimethoxybenzyl groups, which might be selectively removed by different pathways, for some miscellaneous examples see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.