(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Base Information

Chemical Name:(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane
CAS No.:116005-53-9
Molecular Formula:C₃₇H₄₉N₃O₆Si
Molecular Weight:659.898
Hs Code.:

(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Synonyms:(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Suppliers and Price of (+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

There total 10 articles about (+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane 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: 62.0%

: 87-52-5
3-(Dimethylaminomethyl)indole

: 116005-50-6,116126-23-9
6-<(2E)-4-<(tert-butyldimethylsilyl)oxy>but-2-enyl>-3-(carbomethoxy)-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

: 116005-53-9
(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Guidance literature:: With tributylphosphine; In acetonitrile; for 7h; Heating;

Reference yield:

: 116005-52-8
(-)-2,5-diketo-6-(R)-allyl-4-(methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

: 116005-53-9
(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / O₃ / methanol

2: 2.) NaBH₄ / 2.) EtOH

3: 1.) Et₃N, DMAP, 2.) n-BuLi / 1.) CH₂Cl₂, 2.) THF

4: 62 percent / Bu₃P / acetonitrile

With dmap; sodium tetrahydroborate; n-butyllithium; tributylphosphine; ozone; triethylamine; In methanol; acetonitrile;
DOI:10.1021/ja00225a069

Reference yield:

: 116051-29-7
(-)-2,5-diketo-6-(R)-(formylmethyl)-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

: 116005-53-9
(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Guidance literature:: Multi-step reaction with 3 steps

1: 2.) NaBH₄ / 2.) EtOH

2: 1.) Et₃N, DMAP, 2.) n-BuLi / 1.) CH₂Cl₂, 2.) THF

3: 62 percent / Bu₃P / acetonitrile

With dmap; sodium tetrahydroborate; n-butyllithium; tributylphosphine; triethylamine; In acetonitrile;
DOI:10.1021/ja00225a069