메뉴 건너뛰기




Volumn 74, Issue 5, 2009, Pages 1964-1970

Reductions of aliphatic and aromatic nitriles to primary amines with diisopropylaminoborane

Author keywords

[No Author keywords available]

Indexed keywords

ALIPHATIC NITRILES; AMBIENT CONDITIONS; AMBIENT TEMPERATURES; AROMATIC NITRILES; AROMATIC RINGS; BENZONITRILES; BENZYL CYANIDES; BENZYLAMINES; CATALYTIC AMOUNTS; ELECTRON-DONATING GROUPS; ELECTRON-WITHDRAWING GROUPS; ELECTRON-WITHDRAWING SUBSTITUENTS; HIGHER YIELDS; LITHIUM BOROHYDRIDE; LITHIUM IONS; METHOXYBENZONITRILE; METHYL IODIDES; MULTIFUNCTIONAL COMPOUNDS; NITRILE GROUPS; PRIMARY AMINES; REDUCING SYSTEMS; REFLUXING; SELECTIVE REDUCTIONS; TETRAHYDROFURAN; TETRAPHENYLBORATE; TRIMETHYLSILYL CHLORIDES;

EID: 64249093753     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8023329     Document Type: Article
Times cited : (80)

References (31)
  • 1
    • 64249098615 scopus 로고    scopus 로고
    • Aliphatic Amines In Ullmann's Encyclopedia of Industrial Chemistry, 7th ed.; Wiley-VCH: Weinheim, Germany, 2008; AZ p 2.
    • Aliphatic Amines In Ullmann's Encyclopedia of Industrial Chemistry, 7th ed.; Wiley-VCH: Weinheim, Germany, 2008; Vol. AZ p 2.
  • 4
    • 0002204826 scopus 로고
    • Trost, R. M, Fleming, I, Eds, Pergamon: Oxford, UK
    • (b) Mitsunobu, O. Comprehensive Organic Synthesis; Trost, R. M., Fleming, I., Eds.; Pergamon: Oxford, UK, 1991; Vol. 6, p 65.
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 65
    • Mitsunobu, O.1
  • 15
    • 0001588329 scopus 로고    scopus 로고
    • Reductions in Organic Chemistry
    • 2nd ed, American Chemical Society: Washington, DC
    • (a) Hudlicky, M. Reductions in Organic Chemistry, 2nd ed.; ACS Monograph 188; American Chemical Society: Washington, DC, 1996.
    • (1996) ACS Monograph , vol.188
    • Hudlicky, M.1
  • 23
    • 64249114447 scopus 로고    scopus 로고
    • It should be noted that BH2N(ZPr)2 can be prepared from iPrLAB and TMSCl by using a slight excess of n-BuLi so that it contains a catalytic amount of LiBH4. BH2N(ZPr)2 prepared in this manner is also able to reduce nitriles with no additives
    • 2 prepared in this manner is also able to reduce nitriles with no additives.
  • 30
    • 64249114448 scopus 로고    scopus 로고
    • The crude yield of phene thy lamine is reported. A small amount of the crude phenethylamine was purified by forming the oxalate salt and then recrystalizing from methanol
    • The crude yield of phene thy lamine is reported. A small amount of the crude phenethylamine was purified by forming the oxalate salt and then recrystalizing from methanol.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.