Synthetic Communications
 1993
DOI: 10.1080/00397919308011135
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Asymmetric Synthesis. XVIII. Stereocontrolled Synthesis of α-Substituted-2-furfurylamines via Chiral Intermediates

Liu Shikui
1
,
Aiqiao Mi
2
,
Wu Lanjun
3
et al.
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Cited by 10 publications
(1 citation statement)
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“…Following the same methodology, homochiral (R)-αallyl-2-furfurylamine was prepared in 48% (96% ee) yields from the pinanone ketimine, derived from 2-furfurylamine [77].…”
Section: [33]-sigmatropic Rearrangement Of N-protectedmentioning
confidence: 99%

Recent advancements in the homoallylamine chemistry

Puentes
1
,
Kouznetsov
2
2002
Journal of Heterocyclic Chem
153
1
63
1
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“…Following the same methodology, homochiral (R)-αallyl-2-furfurylamine was prepared in 48% (96% ee) yields from the pinanone ketimine, derived from 2-furfurylamine [77].…”
Section: [33]-sigmatropic Rearrangement Of N-protectedmentioning
confidence: 99%

Recent advancements in the homoallylamine chemistry

Puentes
1
,
Kouznetsov
2
2002
Journal of Heterocyclic Chem
153
1
63
1
View full textAdd to dashboardCite
show abstract

Wasser als kritische Größe in der asymmetrischen Allylborierung vonN-Trimethylsilylbenzaldiminen mitB-Allyldiisopinocampheylboran

Chen
1
,
Ramachandran
2
,
Brown
3
1999
Angewandte Chemie
8
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ChemInform Abstract: Asymmetric Synthesis. Part 38. Stereocontrolled Synthesis of α‐ Substituted 2‐Furfurylamines via Chiral Intermediates.

Sh
1
,
Mi
2
,
Wu
3
et al. 1994
ChemInform
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0
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