Add to ORKGSummary: The reaction of nucleophiles with bridgehead bromides 3 and 4 affords rearrangement products resulting from addition of the nucleophile to the carbonyl group followed by ring contraction. This rearrangement has been employed in a direct synthesis of epi-modhephene
The BF₃-catalysed rearrangements of three epoxy-cholestanes have been reinvestigated. The products i...
This thesis is concerned with the synthesis and radical cyclisations of compounds containing a methy...
The cyclopropyl carbinols 8 and 9 obtained by either borohydride reduction (or Grignard addition) of...
Summary: The reaction of nucleophiles with bridgehead bromides 3 and 4 affords rearrangement product...
A Synthesis of modhephene has been achieved, the key feature of which is the use of a novel nucleoph...
The stereochemistry of reaction of phenylmagnesium bromide with camphor (43) has been determined. Th...
The rearrangement of 7,7-dibromonorcar-2-ene to syn-7-bromo-7-methylnorbornene upon treatment with M...
Treatment of (+)-methylenecamphor (2) with NBS in the presence of pyridine resulted in a rapid and r...
A series of macrocycles were successfully prepared using electrophilic halogen-mediated semipinacol ...
A novel protocol for the oxidative rearrangement of alkenes using in situ generated hypervalent iodi...
A novel protocol for the oxidative rearrangement of alkenes using in situ generated hypervalent iodi...
In 1941, Arnold, Bank and Liggett suggested that the formation of allylbenzene from the reaction of ...
A convenient method for the two-step synthesis of arenediynes from 1,2-arenedialdehydes is reported...
In 1941, Arnold, Bank and Liggett suggested that the formation of allylbenzene from the reaction of ...
AbstractA novel protocol for the oxidative rearrangement of alkenes using in situ generated hyperval...
The BF₃-catalysed rearrangements of three epoxy-cholestanes have been reinvestigated. The products i...
This thesis is concerned with the synthesis and radical cyclisations of compounds containing a methy...
The cyclopropyl carbinols 8 and 9 obtained by either borohydride reduction (or Grignard addition) of...
Summary: The reaction of nucleophiles with bridgehead bromides 3 and 4 affords rearrangement product...
A Synthesis of modhephene has been achieved, the key feature of which is the use of a novel nucleoph...
The stereochemistry of reaction of phenylmagnesium bromide with camphor (43) has been determined. Th...
The rearrangement of 7,7-dibromonorcar-2-ene to syn-7-bromo-7-methylnorbornene upon treatment with M...
Treatment of (+)-methylenecamphor (2) with NBS in the presence of pyridine resulted in a rapid and r...
A series of macrocycles were successfully prepared using electrophilic halogen-mediated semipinacol ...
A novel protocol for the oxidative rearrangement of alkenes using in situ generated hypervalent iodi...
A novel protocol for the oxidative rearrangement of alkenes using in situ generated hypervalent iodi...
In 1941, Arnold, Bank and Liggett suggested that the formation of allylbenzene from the reaction of ...
A convenient method for the two-step synthesis of arenediynes from 1,2-arenedialdehydes is reported...
In 1941, Arnold, Bank and Liggett suggested that the formation of allylbenzene from the reaction of ...
AbstractA novel protocol for the oxidative rearrangement of alkenes using in situ generated hyperval...
The BF₃-catalysed rearrangements of three epoxy-cholestanes have been reinvestigated. The products i...
This thesis is concerned with the synthesis and radical cyclisations of compounds containing a methy...
The cyclopropyl carbinols 8 and 9 obtained by either borohydride reduction (or Grignard addition) of...