95308-53-5

Upstream product

• 95308-46-6 methyl 2-azido-3,4-di-O-benzyl-2,6-dideoxy-α-D-arabinohex-5-enopyranoside 
• 95308-48-8 2S-(2β,3β,4α,5α) 4-azido-5-hydroxy-2,3-bis(phenylmethoxy)-cyclohexanone 

Downstream Products

• 153165-83-4 1R-(1β,4α,5β,6β) 4-azido-5,6-bis(phenylmethoxy)-2-cyclohexen-1-ol 
• 153221-61-5 <1R-(1α,4α,5β,6β)> N-<5,6-bis(phenylmethoxy)-4-hydroxy-2-cyclohexen-1-yl>-2,3,4-tris-(methoxy)-benzamide 
• 153165-93-6 <1R-(1α,4β,5β,6β)> N-<5,6-bis(phenylmethoxy)-4-hydroxy-2-cyclohexen-1-yl>-2,3,4-tris-(methoxy)-benzamide 
• 153221-59-1 <1R-(1α,4α,5β,6β)> N-<5,6-bis(phenylmethoxy)-4-hydroxy-2-cyclohexen-1-yl>-1,3 benzodioxole-4-hydroxy-5-carboxamide 
• 153165-91-4 <1R-(1α,4β,5β,6β)> N-<5,6-bis(phenylmethoxy)-4-hydroxy-2-cyclohexen-1-yl>-1,3 benzodioxole-4-hydroxy-5-carboxamide 
• 153165-92-5 <1R-(1α,4β,5β,6β)> N-<5,6-bis(phenylmethoxy)-4-hydroxy-2-cyclohexen-1-yl>-3,4-bis-(methoxy)-benzamide 
• 153221-53-5 <1R-(1α,4α,5β,6β)> N-<5,6-bis(phenylmethoxy)-4-hydroxy-2-cyclohexen-1-yl>-benzamide 
• 153165-89-0 <1R-(1α,4β,5β,6β)> N-<5,6-bis(phenylmethoxy)-4-hydroxy-2-cyclohexen-1-yl>-benzamide 
• 153221-51-3 1S-(1α,4α,5β,6β) 4-amino-5,6-bis(phenylmethoxy)-2-cyclohexen-1-ol 
• 153165-85-6 1R-(1β,4α,5β,6β) 4-amino-5,6-bis(phenylmethoxy)-2-cyclohexen-1-ol 
• 153165-87-8 1S-(1α,4α,5β,6β) 4-azido-5,6-bis(phenylmethoxy)-1-benzoyl-2-cyclohexene 

Relevant academic research and scientific papers

Enantiospecific synthesis and biological evaluation of seco analogues of antitumor amaryllidaceae alkaloids

Some "seco" analogues of Amaryllidaceae alkaloids narciclasine and lycoricidine have been prepared in enantiomerically pure form from D-glucose using Ferrier carbocyclization as the key step. N-acylation of the resulting amines 21, 22, 25 and 26 with seve

Chiral Cyclohexanes From Carbohydrates: Successful Carbocyclisation of a D-Arabino-Hex-5-enopyranoside Derivative

Carbocyclisation of a hex-5-enopyranoside of D-arabino configuration under modified Ferrier's conditions gave chiral substituted cyclohexanes, which are precursors of aminocyclitols and useful synthetic intermediates, in good yield and without side reacti