903907-74-4

Usage

Uses

Used in Pharmaceutical Industry:
(3R,4R,5S)-4-acetylamino-5-amino-3-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester is used as a pharmaceutical intermediate for the development of new drugs, leveraging its unique functional groups and cyclohexene ring structure to create novel therapeutic agents.
Used in Biochemical Research:
In biochemical research, (3R,4R,5S)-4-acetylamino-5-amino-3-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester serves as a key compound for studying enzyme interactions, protein binding, and other biological processes due to its reactive functional groups and structural features.
Used in Organic Synthesis:
(3R,4R,5S)-4-acetylamino-5-amino-3-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester is utilized as a precursor in organic synthesis for the creation of complex organic molecules, taking advantage of its versatile functional groups and cyclohexene ring to form a variety of chemical products.

Upstream product

• 1333341-63-1 (3R,4R,5S)-ethyl 5-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-acetamido-3-hydroxycyclohex-1-enecarboxylate 
• 1333341-62-0 (3R,4R,5S)-ethyl 5-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-acetamido-3-(tert-butyldimethylsilyloxy)cyclohex-1-enecarboxylate 
• 903907-85-7 [(1R,2S)-2-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-1-((R)-1-methoxymethoxy-allyl)-pent-4-enyl]carbamic acid tert-butyl ester 
• 903907-81-3 [(2R)-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-(1R)-((1R)-hydroxy-allyl)-pent-4-enyl]carbamic acid tert-butyl ester 
• 903907-79-9 tert-butyl (R)-4-((S)-11,11-dimethyl-7-methylene-3-oxo-1,10,10-triphenyl-2,9-dioxa-4-aza-10-sila dodecan-5-yl)-2,2-dimethyloxazolidine-3-carboxylate 
• 903907-86-8 [(1R,2R,6S)-6-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-2-methoxymethoxy-cyclohex-3-enyl]carbamic acid tert-butyl ester 
• 903907-80-2 [(2S)-benzyloxycarbonylamino-4-(tert-butyldiphenylsilanyloxymethyl)-(1R)-hydroxymethyl-pent-4-enyl]carbamic acid tert-butyl ester 
• 903907-89-1 (3R,4R,5S)-5-benzyloxycarbonylamino-4-tert-butyloxycarbonylamino-3-methoxymethoxy-cyclohex-1-enecarboxylic acid ethyl ester 
• 903907-88-0 (3R,4R,5S)-5-Benzyloxycarbonylamino-4-tert-butoxycarbonylamino-3-methoxymethoxy-cyclohex-1-enecarboxylic acid 
• 903907-87-9 ((1S,5R,6R)-6-tert-butyloxycarbonylamino-3-hydroxymethyl-5-methoxymethoxy-cyclohex-3-enyl)carbamic acid benzyl ester 
• 903907-90-4 (3R,4R,5S)-4-acetylamino-5-benzyloxycarbonylamino-3-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester 

Relevant academic research and scientific papers

Diversity-oriented production of metabolites derived from chorismate and their use in organic synthesis

Biosynthesis as a model: Based on the branched structure of biosynthetic pathways, such as the shikimate pathway, the selective bioproduction of a set of diverse metabolites has been achieved by means of metabolic engineering (see scheme). A scale-up for

Ring-closing metathesis-based synthesis of (3R,4R,5S)-4-acetylamino-5- amino-3-hydroxy-cyclohex-1-ene-carboxylic acid ethyl ester: A functionalized cycloalkene skeleton of GS4104

(3R,4R,5S)-4-Acetylamino-5-amino-3-hydroxy-cyclohex-1-ene-carboxylic acid ethyl ester, a functionalized cyclohexene skeleton of GS4104, was diastereoselectively synthesized. A major advantage of this synthesis is the use of readily available L-serine to r