86996-96-5

Upstream product

• 86996-94-3 (-)-herbertenolide 

Downstream Products

• 81784-14-7 1-methoxy-12-oxoherbertene 
• 81784-12-5 (-)-α-bromoherbertenol 
• 81784-18-1 (-)-α-formylherbertenol 
• 81784-13-6 (1S)-1,2,2-trimethyl-1-(2-methoxy-5-methyl)phenylcyclopentane 
• 103412-34-6 1-(3,5-dinitrobenzoyloxy)herbertene 
• 103412-33-5 1-benzoyloxy-2-hydroxy-herbertene 
• 103412-31-3 2-benzoyloxy-1-hydroxy-herbertene 
• 103412-30-2 (-)-1,2-diacetoxyherbertene 
• 103412-35-7 1-methoxy-12-norherbertene 
• 103412-32-4 1,2-dibenzoyloxyherbertene 
• 86996-98-7 14-ethylthio-1-hydroxyherbertene 
• 86996-95-4 (S)-5-methyl-3-(1,2,2-trimethylcyclopentyl)benzene-1,2-diol 
• 81784-10-3 4-methyl-2-[(1S)-1,2,2-trimethylcyclopentyl]phenol 
• 86996-97-6 14-hydroxy-1-methoxyherbertene 

Relevant academic research and scientific papers

(-)-HERBERTENEDIOL AND (-)-HERBERTENOLIDE, TWO NEW SESQUITERPENOIDS OF THE ENT-HERBERTANE CLASS FROM THE LIVERWORT HERBERTA ADUNCA

The structures of (-)-herbertenediol and (-)-herbertenolide, the new aromatic sesquiterpenoids with the ent-herbertane skeleton isolated from the liverwort Herberta adunca, have been determined on the basis of the chemical and spectral evidence.

Structures of ent-Herbertane Sesquiterpenoids displaying Antifungal Properties from the Liverwort Herberta adunca

Several aromatic sesquiterpenoids displaying antifungal propaerties have been isolated from the liverwort Herberta adunca together with a mother hydrocarbon with a novel irregular sesquiterpene skeleton, ent-herbertane, and their structures and absolute configurations have been determined on the basis of extensive degradation reactions and spectroscopic evidence.The biological activity is also described.