Some phospholene oxides were transformed into the corresponding phosph
ine-boranes. The reaction of a 2-phospholene-borane with dichlorocarbe
ne gave the phospholene- and the phospholane-dichloromethyl-boranes as
the major products, and the cyclopropane derivative as the minor comp
onent. A similar reaction of 3-phospholene-boranes afforded only the p
hopholene- and the phospholane-dichloromethyl-boranes. A phosphabicycl
ohexane-borane was synthesized from the P-oxide by change in the funct
ionality. The dihydrophosphinine-boranes were prepared by cyclopropane
ring opening of a phosphabicyclohexane, or by change in the functiona
lity of the dihydrophosphinine oxides. The reaction of dihvdrophosphin
ine-boranes with dichlorocarbene did not result in the formation of th
e desired phosphepine. This species was eventually synthesized by chan
ge in the functionality of the P-oxide. The preparation of unsaturated
phosphine-boranes was usually complicated by reduction side-reactions
.