메뉴 건너뛰기




Volumn 16, Issue 43, 2010, Pages 12797-12800

The development of a general strategy for the synthesis of tyramine-based natural products by using continuous flow techniques

Author keywords

flow chemistry; Heck reaction; microwave chemistry; tyramine

Indexed keywords

CONTINUOUS FLOW TECHNIQUE; FLOW CHEMISTRY; GRAM SCALE; HECK COUPLING REACTION; HECK REACTION; HIGH TEMPERATURE; MICROWAVE CHEMISTRY; MULTI-STEP; NATURAL PRODUCTS; PROOF OF CONCEPT; ROOM TEMPERATURE; SYNTHETIC PROTOCOLS; TYRAMINE;

EID: 78449291149     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002102     Document Type: Article
Times cited : (32)

References (37)
  • 1
    • 78449295362 scopus 로고    scopus 로고
    • For recent reviews on flow chemistry, see
    • For recent reviews on flow chemistry, see
  • 12
    • 33746216295 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 2761 - 2766
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2761-2766
  • 16
    • 78449301809 scopus 로고    scopus 로고
    • For examples of natural products synthesis conducted in flow, see
    • For examples of natural products synthesis conducted in flow, see
  • 23
    • 78449289571 scopus 로고    scopus 로고
    • For the isolation of N-trans-feruloyl tyramine and N-trans-coumaroyl tyramine, see
    • For the isolation of N-trans-feruloyl tyramine and N-trans-coumaroyl tyramine, see
  • 26
  • 29
    • 30444442984 scopus 로고    scopus 로고
    • For the use of tyramines to inhibit acetylcholinesterase, see:, - 738
    • For the use of tyramines to inhibit acetylcholinesterase, see:, D. K. Kim, K. Lee, Arch. Pharmacal Res. 2003, 26, 735 - 738.
    • (2003) Arch. Pharmacal Res. , vol.26 , pp. 735
    • Kim, D.K.1    Lee, K.2
  • 30
    • 0141849446 scopus 로고    scopus 로고
    • For the use of tyramines to inhibit nitric oxide synthase, see:, - 985
    • For the use of tyramines to inhibit nitric oxide synthase, see:, Y. Kim, M. S. Han, S. Lee, J. Kim, Y. C. Kim, Phytother. Res. 2003, 17, 983 - 985.
    • (2003) Phytother. Res. , vol.17 , pp. 983
    • Kim, Y.1    Han, M.S.2    Lee, S.3    Kim, J.4    Kim, Y.C.5
  • 31
    • 78449281598 scopus 로고    scopus 로고
    • note
    • Tyramine, or one of its analogues (1.0equiv) was reacted with acryloyl chloride (1.0equiv) and Hunig's base (1.1equiv) in DMF. The crude amide was used directly in the subsequent Heck reaction.
  • 32
    • 78449303293 scopus 로고    scopus 로고
    • For other examples of the Heck reaction performed by using flow techniques, see
    • For other examples of the Heck reaction performed by using flow techniques, see
  • 35
    • 78449297110 scopus 로고    scopus 로고
    • For complete experimental details and full spectral characterization of all new compounds, see the Supporting Information
    • For complete experimental details and full spectral characterization of all new compounds, see the Supporting Information.
  • 36
    • 78449288609 scopus 로고    scopus 로고
    • For the structure of the double-Heck product and full spectral characterization, see the Supporting Information
    • For the structure of the double-Heck product and full spectral characterization, see the Supporting Information.
  • 37
    • 56949098267 scopus 로고    scopus 로고
    • During the course of our studies, the first synthesis of aplysamine 6 was reported, see:, - 160
    • During the course of our studies, the first synthesis of aplysamine 6 was reported, see:, N. Ullah, K. M. Arafeh, Tetrahedron Lett. 2009, 50, 158 - 160.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 158
    • Ullah, N.1    Arafeh, K.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.