Efficient synthesis of optically active 2-amino-2'-diphenylphosphino-1,1'-binaphthyl and its derivatives

2000 ◽  
Vol 78 (6) ◽  
pp. 697-703 ◽  
Author(s):  
Kenzo Sumi ◽  
Takao Ikariya ◽  
Ryoji Noyori

Optically active 2-amino-2'-diphenylphosphino-1,1'-binaphthyls having various functional groups, such as amino, alkoxycarbonylamino, acylamino, mono- and dialkylamino, and sulfonylamino at C2 position were prepared. The key intermediate of the above aminophosphines was 2-carbamoyl-2'-diphenylphosphinyl-1,1'-binaphthyl synthesized from optically active 2-cyano-2'-diphenylphosphinyl-1,1'-binaphthyl. The transformation of the carbamoyl group to an amino group was effected by the Hofmann reaction.Key words: aminophosphine ligand, Hofmann reaction, optically active phosphine ligand.

ChemInform ◽  
2005 ◽  
Vol 36 (8) ◽  
Author(s):  
J. S. Yadav ◽  
B. V. S. Reddy ◽  
G. Satheesh ◽  
P. Naga Lakshmi ◽  
S. Kiran Kumar ◽  
...  

Heterocycles ◽  
1992 ◽  
Vol 33 (2) ◽  
pp. 831 ◽  
Author(s):  
Seiichi Takano ◽  
Masashi Akiyama ◽  
Takumichi Sugihara ◽  
Kunio Ogasawara

Synthesis ◽  
1983 ◽  
Vol 1983 (08) ◽  
pp. 676-678 ◽  
Author(s):  
Jean-Alain Fehrentz ◽  
Bertrand Castro

Synlett ◽  
2019 ◽  
Vol 30 (20) ◽  
pp. 2273-2278 ◽  
Author(s):  
Piroska Gyárfás ◽  
János Gerencsér ◽  
Warren S. Wade ◽  
László Ürögdi ◽  
Zoltán Novák ◽  
...  

An efficient method for nucleophilic aromatic substitution on 7-azaindoles has been developed. The reaction is facilitated by the unique dual influence of SEM as both protecting and activating group, permitting mild conditions and short reaction times that are compatible with sensitive functional groups. The method is suitable for the synthesis of a broad range of products, most notably ethers.


1986 ◽  
Vol 17 (50) ◽  
Author(s):  
N. TAMURA ◽  
Y. KAWANO ◽  
Y. MATSUSHITA ◽  
K. YOSHIOKA ◽  
M. OCHIAI

Synthesis ◽  
1991 ◽  
Vol 1991 (02) ◽  
pp. 162-164 ◽  
Author(s):  
M. Larchevêque ◽  
Y. Petit

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