97552-35-7

Upstream product

• 97552-22-2 trans-3-<1-(hydroxymethyl)-1(E)-propenyl>-6-oxabicyclo<3.1.0>hexane 
• 97552-24-4 (2R^*,3S^*)-ethyl-2-(3-cyclopentenyl)-3-hydroxybutanoate 
• 97552-31-3 (E,3aR^*,5S^*,6aS^*)-3-(phenylmethyl)-2-oxo-3,3a,4,5,6,6a-hexahydro-5-<1-<<(triisopropylsilyl)oxy>methyl>propenyl>-6a-<2-(trimethylacetamido)benzoyl>-2H-cyclopentoxazole 
• 97552-32-4 (E,3aR^*,5S^*,6aR^*)-3-(phenylmethyl)-2-oxo-3,3a,4,5,6,6a-hexahydro-5-<1-<<(triisopropylsilyl)oxy>methyl>propenyl>-6a-<1-<2-(trimethylacetamido)phenyl>ethenyl>-2H-cyclopentoxazole 
• 97570-06-4 (E,3aR^*,5R^*,6aS^*)-6a-<(2-aminophenyl)ethenyl>-3-(phenylmethyl)-5-<1-<<(tert-butyldimethylsilyl)oxy>methyl>propenyl>-3,3a,4,5,6,6a-hexahydro-2H-cyclopentoxazole 
• 97570-05-3 (E,2S^*,4R^*)-2--4-<1-<<(triisopropylsilyl)oxy>methyl>propenyl>cyclopentan-1-one 
• 97552-30-2 (E,1R^*,2R^*,4S^*)-2--1-hydroxy-4-<1-<<(triisopropylsilyl)oxy>methyl>propenyl>cyclopentane 
• 97552-33-5 (E,3aR^*,5R^*,6aS^*)-6a-<1-<2-aminophenyl>ethenyl>-5-<1-(hydroxymethyl)propenyl>-3-(phenylmethyl)-3,3a,4,5,6,6a-hexahydro-2H-cyclopentoxazole 
• 97552-20-0 (E,3aR^*,5S^*,11bS^*)-5-<1-(hydroxymethyl)propenyl>-2,3,3a,4,5,6-hexahydro-3-(phenylmethyl)-1H-pyrrolo<2,3-d>carbazole 
• 97552-34-6 (1S,2S,4R)-1-[1-(2-Amino-phenyl)-vinyl]-2-benzylamino-4-((E)-1-hydroxymethyl-propenyl)-cyclopentanol 
• 97552-29-9 (1R,2R,4S)-2-Benzylamino-4-((E)-1-triisopropylsilanyloxymethyl-propenyl)-cyclopentanol 
• 97552-43-7 (2S,3R)-2-Cyclopent-3-enyl-3-methanesulfonyloxy-butyric acid ethyl ester 
• 97552-27-7 (E)-trans-3-<1-<<(triisopropylsilyl)oxy>methyl>-1(E)-propenyl>-6-oxabicyclo<3.1.0>hexane 
• 97552-26-6 trans-3-(1-carbethoxy-1(E)-propenyl)-6-oxabicyclo<3.1.0>hexane 

Downstream Products

• 97552-36-8 (E,3aR^*,5S^*,6aR^*,11bS^*)-5-<1-<<(tert-butyldimethylsilyl)oxy>methyl>propenyl>-7-(methoxycarbonyl)-3-(phenylmethyl)-2,3,3a,4,5,6,6a,7-octahydro-1H-pyrrolo<2,3-d>carbazole 

Relevant academic research and scientific papers

Synthesis Applications of Cationic Aza-Cope Rearrangements. Stereocontrolled Synthesis of Hexahydro-1H-pyrrolocarbazoles

The synthesis of a series of 5-substituted octahydro-1H-pyrrolocarbazoles 4, potential intermediates for the synthesis of the Strychnos alkaloid akuammicine 2, is described.The known β-keto ester 9 was converted to the (E)-epoxy alcohol 7 in 39perc