Direct Conversion of Nitroalkenes to Carbonyl Compounds:

Hass, H. B., A. G. Susie, and R. L. Heider J. Org. Chem., 15, 8 (1950)
Nightingale, D., and J. R. James. J. Am. Chem. Soc., 55, 352 (1944)
Torii, S., H. Tanaka, and T. Katoh. Chem. Lett., 607 (1983)
Bordoloi, M. J. Chem. Soc., Chem. Common, 922 (1993)
Mourad, M. S., R. S. Varma, and G. W Kabalka Synthesis, 654 (1985 )
Varma, R. S., M. Barma, and G. W Kabalka. Tetrahedron Lett, 26, 3777 (1985)
Monti, D.,P. Gramatica, G. Speranza, and P. Manitto - Tetrahedron Lett., 24,417(1983)

Somebody can send me this literature ?

The ebook "The Nitro Group in Organic Synthesis" reports on page 165 yields from 80 to 88% of Carbonyl Compounds and ref. the literature in my thread. I want to find the way for high yields.

Hass, H. B., A. G. Susie, and R. L. Heider J. Org. Chem., 15, 8 (1950)

Post 389629

(Barium: "PNP and P2P", Stimulants)

Mourad, M. S., R. S. Varma, and G. W Kabalka Synthesis, 654 (1985 )

Post 394699

(demorol: "Nitroalkene reduction using trialkylborohydrides", Novel Discourse)

References for Conversion of Nitroalkenes to Carbonyl Compounds (djvu articles courtesy of lugh)

JOC 15, 8-14 (1950)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/nitrostyrenes.fe-hcl.pdf)

Synthesis, 654 (1985)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/p2p.l-selectride.pdf)

JACS 66 352-354 (1944)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/nightingale.djvu)

Chem. Lett. 607 (1983)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/torii.djvu)

Tet. Lett. 26, 3777 (1985)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/varma.djvu)

J. Chem. Soc. Chem. Commun. 922 (1993)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/bordoloi.djvu)

Tetrahedron Lett. 24, 417(1983)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/monti.djvu)

(All *.djvu articles can be viewed with the browser plugin found at

http://www.djvu.com/download/

)