US EPA

7551788 

Journal Article 

Synthesis of New Active o ‐Nitrophenyl Carbamates 

Simon, M; Csunderlik, C; Cotarca, L; Căproiu, MT; Neda, Ion; Turoczi, MC; Volpicelli, R; , 

2005 

1 

Synthetic Communications
ISSN: 0039-7911 

TAYLOR & FRANCIS INC 

PHILADELPHIA 

35 

11 

1471-1479 

English 

10.1081/SCC-200057986 

WOS:000230107300007 

http://www.tandfonline.com/doi/abs/10.1081/SCC-200057986
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A very high-yielding reaction of bis(o-nitrophenyl) carbonate with aliphatic amines under mild conditions has been developed. The resulting o-nitrophenyl carbamates were characterized by IR, H-1-NMR, C-13-NMR, and elemental analysis. 

Bis(o-nitrophenyl) carbonate; O-nitrophenyl carbamates; Phosgene-free carbonylations; Triphosgene; bis(2 nitrophenyl)carbonate; carbamic acid derivative; carbonic acid derivative; n benzyl 2 nitrophenyl carbamate; n butyl 2 nitrophenyl carbamate; n cyclohexyl 2 nitrophenyl carbamate; n isobutyl 2 nitrophenyl carbamate; n isopenthyl 2 nitrophenyl carbamate; n isopropyl 2 nitrophenyl carbamate; n isopropyl 4 nitrophenyl carbamate; n propyl 2 nitrophenyl carbamate; n propyl 4 nitrophenyl carbamate; n sec butyl 2 nitrophenyl carbamate; n,n dibenzyl 2 nitrophenyl carbamate; n,n diisobutyl 2 nitrophenyl carbamate; n.n' dicyclohexylurea; unclassified drug; article; carbon nuclear magnetic resonance; chemical analysis; chemical structure; infrared radiation; proton nuclear magnetic resonance; synthesis