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Volumn 60, Issue 46 SPEC. ISS., 2004, Pages 10385-10396

Conversion of chiral unsaturated cyanohydrins into chiral carba- and heterocycles via ring-closing metathesis

Author keywords

Cyanohydrins; Cyclic ethanolamines; Heterocycles; Ring closing metathesis

Indexed keywords

1 BENZYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 1,2,3,6 TETRAHYDROPYRIDIN 3 OL; 1 BENZYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 2,3,4,7 TETRAHYDROAZEPINE; 2 [(TERT BUTYLDIPHENYLSILYL)OXY]HEX 5 ENE NITRILE; 2 [(TERT BUTYLDIPHENYLSILYL)OXY]PENT 3 ENE NITRILE; ALCOHOL DERIVATIVE; ALLYLAMINE; BENZYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 2,3,4,7 TETRAHYDRO 1H AZEPINE 1 CARBOXYLATE; BENZYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 3,4,5,8 TETRAHYDROAZOCINE 1(2H) CARBOXYLATE; BENZYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 3,6 DIHYDROPYRIDINE 1(2H) CARBOXYLATE; BENZYL 6 [(TERT BUTYLDIPHENYLSILYL)OXYCYCLOHEX 3 EN 1 YL]CARBAMATE; BENZYL[(TERT BUTYLDIPHENYLSILYL)OXYCYCLOHEPT 3 EN 1 YL]CARBAMATE; BENZYL[(TERT BUTYLDIPHENYLSILYL)OXYCYCLOHEPT 4 EN 1 YL]CARBAMATE; BENZYL[(TERT BUTYLDIPHENYLSILYL)OXYCYCLOOCTA 4 EN 1 YL]CARBAMATE; BENZYL[2 (TERT BUTYLDIPHENYLSILYL)OXYCYCLOHEX 3 EN 1 YL]CARBAMATE; BENZYL[2 (TERT BUTYLDIPHENYLSILYL)OXYCYCLOPENT 3 EN 1 YL]CARBAMATE; BORON DERIVATIVE; CYANOHYDRIN; ETHANOLAMINE DERIVATIVE; HYDROGEN; PYRIDINE DERIVATIVE; SODIUM DERIVATIVE; TERT BUTYL 2 [(TERT BUTYLDIPHENYLSILYL)OXYCYCLOHEPT 4 EN 1 YL]CARBAMATE; TERT BUTYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 2,3,4,7 TETRAHYDRO 1H AZEPINE 1 CARBOXYLATE; TERT BUTYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 3,4,5,8 TETRAHYDROAZOCINE 1(2H) CARBOXYLATE; TERT BUTYL 3 [(TERT BUTYLDIPHENYLSILYL)OXY] 3,6 DIHYDROPYRIDINE 1(2H)CARBOXYLATE; TERT BUTYL 6 [(TERT BUTYLDIPHENYLSILYL)OXYCYCLOHEX 3 EN 1 YL]CARBAMATE; TERT BUTYL[(TERT BUTYLDIPHENYLSILYL)OXYCYCLOHEPT 3 EN 1 YL]CARBAMATE; TERT BUTYL[2 (TERT BUTYLDIPHENYLSILYL)OXYCYCLOPENT 3 EN 1 YL]CARBAMATE; UNCLASSIFIED DRUG;

EID: 4944258883     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.07.103     Document Type: Article
Times cited : (25)

References (22)
  • 5
    • 0002509997 scopus 로고    scopus 로고
    • Biocatalysis in the enantioselective formation of chiral cyanohydrins, valuable building blocks in organic chemistry
    • R.N. Patel Marcel Dekker New York
    • J. Brussee, and A. van der Gen Biocatalysis in the enantioselective formation of chiral cyanohydrins, valuable building blocks in organic chemistry R.N. Patel Stereoselective Biocatalysis 2000 Marcel Dekker New York 289 320 Chapter 11
    • (2000) Stereoselective Biocatalysis , pp. 289-320
    • Brussee, J.1    Van Der Gen, A.2
  • 6
    • 0000532201 scopus 로고    scopus 로고
    • Hydroxynitrile lyases in stereo selective synthesis
    • R.N. Patel Marcel Dekker New York
    • F. Effenberger Hydroxynitrile lyases in stereo selective synthesis R.N. Patel Stereoselective Biocatalysis 2000 Marcel Dekker New York 321 342 Chapter 12
    • (2000) Stereoselective Biocatalysis , pp. 321-342
    • Effenberger, F.1
  • 17
    • 4944223984 scopus 로고    scopus 로고
    • note
    • Bis(tricyclohexylphosphine)benzylidine ruthenium(IV) dichloride, Grubbs' catalyst, was obtained from Strem.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.