152365-71-4

Upstream product

• 82518-06-7 3,5,6,8-tetraphenyl-2,9-dithia-1-phosphabicyclo<4.3.0>-nona-3,7-diene 1-sulfide 

Downstream Products

• 632-51-9 1,1,2,2-tetraphenylethylene 
• 1170009-11-6 2,7-dibromo-3',5'-diphenylspiro[fluorene-9,6'-[2]thia[1]phosphabicyclo[3.1.0]hex[3]ene] 
• 1170008-87-3 3',5'-diphenylspiro[fluorene-9,6'-[2]thia[1]phosphabicyclo[3.1.0]hex[3]ene] 

Relevant academic research and scientific papers

Syntheses of 1,2-Thiaphospholes and Their Thermal and Lewis Acid-Promoted Addition Reactions

3,5-Di-substituted 1,2-thiaphospholes were efficiently prepared by treating 2,9-dithia-1-phosphabicyclo-nona-3,7-diene 1-sulfides with n-Bu3P.The thiaphospholes reacted thermally with norbornadiene, norbornene or dietyl azodicarboxylate to produce

Different thermal reactivity of a 1,2-thiaphospholo[a]phosphirane in free and metal carbonyl complexed form

The W(CO)5 and Fe(CO)4 complexes of the bicyclic phosphirane 3,5,6,6-tetraphenyl-1-phospha-2-thiabicyclo-[3.1.0]hex-3-ene undergo a thermal 2-phenylphosphirane → dihydrophosphaisoindole ring expansion, while the free phosphirane suffers both a [2 + 1] cycloreversion and a fragmentation yielding a butadienyl sulfide.

Preparation and Reactions of 1,2-Thiaphospholes

Treatment of 2,9-dithia-1-phosphabicyclo-nona-3,7-diene 1-sulfides with n-Bu3P afforded 1,2-thiaphospholes in good yields.The thiaphospholes reacted thermally with norbornene to produce 1:2 double Diels-Alder cycloadducts, whereas they reacted with