RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2006(19): 3309-3315
DOI: 10.1055/s-2006-950229
DOI: 10.1055/s-2006-950229
SPECIALTOPIC
© Georg Thieme Verlag Stuttgart · New York
Aluminum Amalgam for the Reduction of Sensitive β-Nitroamines to 1,2-Diamines
Weitere Informationen
Received
25 July 2006
Publikationsdatum:
05. September 2006 (online)
Publikationsverlauf
Publikationsdatum:
05. September 2006 (online)
Abstract
A two-step reduction protocol for the conversion of a range of sensitive β-nitroamines to 1,2-diamines has been developed that is operationally simpler, cheaper and higher-yielding than the previously reported SmI2 protocol. Reduction of the nitro function to a hydroxylamine was achieved with Al amalgam and then reduced to the 1,2-diamine product with H2, Pd/C or LiAlH4 with no erosion of diastereoselectivity. A representative selection of 9 β-nitroamines were reduced in 71-94% yield.
Key words
reduction - aluminum - amines - β-nitroamine - 1,2-diamine
- 1
Adams H.Anderson JC.Peace S.Pennell AMK. J. Org. Chem. 1998, 63: 9932 - 2
Anderson JC.Blake AJ.Howell GP.Wilson C. J. Org. Chem. 2005, 70: 549 - 3
Anderson JC.Howell GP.Lawrence RM.Wilson CS. J. Org. Chem. 2005, 70: 5665 - 4
Johnson JS.Evans DA. Acc. Chem. Res. 2000, 33: 325 - The nitro-Mannich reaction had previously been described, but with no reference to stereoselectivity:
-
5a
Henry L. Bull. Acad. Roy. Belg. 1896, 32: 33 -
5b
Senkus M. J. Am. Chem. Soc. 1946, 68: 10 -
5c
Johnson HG. J. Am. Chem. Soc. 1946, 68: 12 -
5d
Johnson HG. J. Am. Chem. Soc. 1946, 68: 14 -
5e
Lambert A.Rose JD. J. Chem. Soc. 1947, 1511 -
5f
Hurd CD.Strong JS. J. Am. Chem. Soc. 1950, 72: 4813 -
5g
Kozlov LM.Fink EF. Tr. Kazan. Khim. Tekhnol. Inst. im. S.M. Kirova 1956, 21: 163 ; Chem. Abstr. 1957, 51, 66364 -
6a
Yamada K.Harwood SJ.Gröger H.Shibasaki M. Angew. Chem. Int. Ed. 1999, 38: 3504 -
6b
Yamada K.Moll G.Shibasaki M. Synlett 2001, 980 -
6c
Knudsen KR.Risgaard T.Nishiwaki N.Gothelf KV.Jørgensen KA. J. Am. Chem. Soc. 2001, 123: 5843 -
6d
Nishiwaki N.Knudsen KR.Gothelf KV.Jørgensen KA. Angew. Chem. Int. Ed. 2001, 40: 2992 -
6e
Qian C.Gao F.Chen R. Tetrahedron Lett. 2001, 42: 4673 -
6f
Okino T.Nakamura S.Furukawa T.Takemoto Y. Org. Lett. 2004, 6: 625 -
6g
Nugent BM.Yoder RA.Johnston JN. J. Am. Chem. Soc. 2004, 126: 3418 -
6h
Lee A.Kim W.Lee J.Hyeon T.Kim BM. Tetrahedron: Asymmetry 2004, 15: 2595 -
6i
Bernardi L.Bonini BF.Capitò E.Dessole G.Comes-Franchini M.Fochi M.Ricci A. J. Org. Chem. 2004, 69: 8168 -
6j
Yoon TP.Jacobsen EN. Angew. Chem. Int. Ed. 2005, 44: 466 -
6k
Li Z.Li C.-J. J. Am. Chem. Soc. 2005, 127: 3672 -
6l
Knudsen KR.Jørgensen KA. Org. Biomol. Chem. 2005, 3: 1362 -
6m
Ruano JLG.Topp M.López-Cantarero J.Alemán J.Remuiňán MJ.Cid MB. Org. Lett. 2005, 7: 4407 -
6n
Palomo C.Oiarbide M.Laso A.López R. J. Am. Chem. Soc. 2005, 127: 17622 - 7
Larock RC. Comprehensive Organic Transformations Wiley; New York: 1999. 2nd ed. - 8
Sturgess MA.Yarberry DJ. Tetrahedron Lett. 1993, 34: 4743 -
9a
Bhagwatheeswaran H.Gaur SP.Jain PC. Synthesis 1976, 615 -
9b
Tsuritani N.Yamada K.Yoshikawa N.Shibasaki M. Chem. Lett. 2002, 276 - 10
Iffland DC.Cassis FA. J. Am. Chem. Soc. 1952, 74: 6284 - 11
Bunce SC.Clemans SD.Bennett BA. J. Org. Chem. 1975, 40: 961 - 12
Osby JO.Ganem B. Tetrahedron Lett. 1985, 26: 6413 - 13
Johnson K.Degering EF. J. Am. Chem. Soc. 1939, 61: 3194 - 14
Fitch R.Luzzio F. Tetrahedron Lett. 1994, 35: 6013 -
15a
Reduction with Zn (45 equiv) in aq NH4Cl/THF proceeded in 89% yield, but degraded substrate 1h.
-
15b This mild reducing system was reported for N-O bond cleavage:
White JD.Hansen JD. J. Org. Chem. 2005, 70: 1963 - 16
Anderson JC.Peace S.Pih S. Synlett 2000, 850