methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate

Base Information

Chemical Name:methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate
CAS No.:85390-39-2
Molecular Formula:C₁₇H₂₂O₅Se
Molecular Weight:385.319
Hs Code.:

Synonyms:methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate

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Chemical Property of methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate

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Technology Process of methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate

There total 7 articles about methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: 85390-38-1
methyl (1R,2S,3S,4S)-2,3-<(dimethylmethylene)dioxy>-4-formyl-4-(phenylseleno)cyclopentane-1-carboxylate

: 85390-39-2
methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate

Guidance literature:: With sodium tetrahydroborate; In methanol; dichloromethane; at -78 ℃; for 0.25h;
DOI:10.1021/ja00350a050

Reference yield:

: 84955-43-1
(3aS,4R,6S,6aR)-6-Formyl-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxole-4-carboxylic acid

: 85390-39-2
methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 2.42 g

2: 73 percent / p-(dimethylamino)pyridine, triethylamine / tetrahydrofuran / 16 h / Ambient temperature

3: 47.1 percent / silver trifluoroacetate / CH₂Cl₂ / 2 h / Ambient temperature

4: 95 percent / NaBH₄ / CH₂Cl₂; methanol / 0.25 h / -78 °C

With dmap; sodium tetrahydroborate; silver trifluoroacetate; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja00350a050

Reference yield:

: 85390-36-9
methyl (1R,2S,3R,4R)-2,3-<(dimethylmethylene)dioxy>-4-formyl-cyclopentane-1-carboxylate

: 85390-39-2
methyl (1R,2S,3S,4R)-2,3-<(dimethylmethylene)dioxy>-4-(hydroxymethyl)-4-(phenylseleno)cyclopentane-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / p-(dimethylamino)pyridine, triethylamine / tetrahydrofuran / 16 h / Ambient temperature

2: 47.1 percent / silver trifluoroacetate / CH₂Cl₂ / 2 h / Ambient temperature

3: 95 percent / NaBH₄ / CH₂Cl₂; methanol / 0.25 h / -78 °C

With dmap; sodium tetrahydroborate; silver trifluoroacetate; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja00350a050